- freely available
Plants 2013, 2(1), 107-147; doi:10.3390/plants2010107
Abstract: The pollen tube is a fast tip-growing cell carrying the two sperm cells to the ovule allowing the double fertilization process and seed setting. To succeed in this process, the spatial and temporal controls of pollen tube growth within the female organ are critical. It requires a massive cell wall deposition to promote fast pollen tube elongation and a tight control of the cell wall remodeling to modify the mechanical properties. In addition, during its journey, the pollen tube interacts with the pistil, which plays key roles in pollen tube nutrition, guidance and in the rejection of the self-incompatible pollen. This review focuses on our current knowledge in the biochemistry and localization of the main cell wall polymers including pectin, hemicellulose, cellulose and callose from several pollen tube species. Moreover, based on transcriptomic data and functional genomic studies, the possible enzymes involved in the cell wall remodeling during pollen tube growth and their impact on the cell wall mechanics are also described. Finally, mutant analyses have permitted to gain insight in the function of several genes involved in the pollen tube cell wall biosynthesis and their roles in pollen tube growth are further discussed.
Fertilization of flowering plants requires the delivery of two sperm cells carried by the pollen tube, a fast tip-polarized growing cell, to the egg cell. In plants such as Arabidopsis thaliana, this process begins with the adhesion of the pollen grains on the stigmatic papillae after the pollen coat has contacted the papillae (Figure 1a–d). Following hydration of the pollen grain, the pollen tube emerges either from one of the three pollen grain apertures (Figure 1c) or through the exine wall (Figure 1e) . Then, pollen tubes invade the cell wall of the papillae (Figure 1b–d), enter the short style, and grow in the apoplast of the specialized transmitting tract cells (Figure 1b) enriched in extracellular nutrient [2,3].
During this invasive growth, pollen tubes are guided to the ovules via signals that need to pass through the cell wall to reach their membrane-associated or intracellular targets [4,5,6,7,8,9,10,11]. In addition to being the interface between the tube cell and the surrounding (culture medium or female tissues), the cell wall of pollen tubes plays a crucial role in the control of the cell shape, in the protection of the generative cells and in the resistance against turgor pressure induced tensile stress [12,13]. Thus, a tight control of cell wall deposition and remodeling during pollen tube growth is required to fulfill all these functions.
In this review, we describe our current knowledge on the biosynthesis, distribution and biochemistry of cell wall polymers including pectin, hemicellulose, cellulose and callose from several pollen tube species (including plants with dry stigma and solid style like Arabidopsis thaliana and tobacco and wet stigma and hollow style like in lily). The structure and functions of arabinogalactan-proteins in pollen tube growth will not be addressed as it was recently detailed by . Finally, the enzymes from the male gametophyte and the female sporophytic counterpart possibly involved in the cell wall remodeling during pollen tube growth are further discussed in relation with the mechanical properties of the cell wall.
2. Cell Wall Polymers in Pollen Tubes
Despite the importance of pollen tubes for the delivery of the sperm cells to the egg, little is known about the underlying molecular mechanisms that regulate the mechanical interaction of pollen tubes with the female floral tissues and only very scarce data are available concerning the biosynthesis and remodeling of the pollen tube cell wall.
Pollen tubes in most species display in the tip region a clear zone like in A. thaliana (Figure 2a), composed of numerous Golgi-derived vesicles that migrate toward the apex in the cell cortex and accumulate in an annulus-shaped region adjacent to the extreme tip (apical flank) where they fuse with the plasma membrane to sustain pollen tube growth . At the extreme apex and in the distal region of the pollen tube, endocytosis takes place possibly by clathrin-dependent and -independent pathways [10,16,17,18,19].
Transmission electron microscope observations of in vitro and in vivo grown pollen tubes from many species including lily , tobacco [21,22], A. thaliana [23,24,25,26] and in several but not all the gymnosperm investigated species like Pinus sylvestris , Podocarpus nagi or Pinus banksiana  showed a cell wall composed of two layers at the shank of the pollen tube: a fibrillar outer layer and a weakly electron-dense inner wall (Figure 2b). In contrast, the inner cell wall layer is generally lacking at the pollen tube tip in normal condition [20,23,24,27].
2.1. Distribution of Carbohydrate Epitopes in the Pollen Tube Cell Wall
Distribution of pollen tube cell wall polymers was investigated by using mostly cytochemical reagents, enzymes and/or antibodies (Table 1). In most of the immunolocalization studies, monoclonal antibodies (mAbs) are applied on the whole pollen tube [24,25,26,27,28,29,30,31,32], allowing a cell surface labeling that may mislead in the interpretation as epitopes may have been masked by other polymers. To avoid this problem, enzyme treatments were sometimes applied on fixed tubes or pollen tubes were embedded in resin and sectioned . Another possible artifact is caused by the slow penetration of the chemical fixative that arrests pollen tube growth while exocytosis is still ongoing, or the other way round, that arrests of enzymatic reactions in the wall while the tube is still growing.
|Probe a||Polysaccharide b||Epitope recognized c||Refs.|
|LM15||XyG||XXXG, XXLG, XLXG, XXGG|||
|JIM5||weakly methylesterified HG||α-MeGalA-(1→4)-α-GalA(4)-(1→4)-α-MeGalA|||
|LM19||weakly methylesterified HG||α-GalA-(1→4)(4)|||
|JIM7||partially methylesterified HG||α-GalA-(1→4)-α-MeGalA(4)-(1→4)-α-GalA|||
|LM20||partially methylesterified HG||α-MeGalA-(1→4)(4)|||
|LM6||(1→5)-α-l-arabinan (RG-I)||Branched α-Ara-(1→5)(5)|||
|LM13||(1→5)-α-l-arabinan (RG-I)||Linear α-Ara-(1→5)(5)|||
|Anti-RG-II||Monomeric and dimeric RG-II||unknown|||
a CCRC-M. Complex Carbohydrate Research Center-Monoclonal, LM, Leeds Monoclonal, JIM, John Innes Monoclonal, LAMP, LAMinarin Pentaose, RG-II. Rhamnogalacturonan-II, PI. Propidium iodide, CBH-I. Cellobiohydrolase-I, CBM3a. Cellulose binding module3a. b XyG. Xyloglucan, HG. Homogalacturonan, RG-I. Rhamnogalacturonan-I. c Ara. arabinose, Fuc. fucose, Gal. galactose, GalA. galacturonic acid, Glc, glucose, MeGalA, 6-O-methyl-galacturonate, na. not applicable. For more information see .
Distribution of cell wall polymers in pollen tubes was investigated in plant species of the angiosperm eudicots such as A. thaliana [23,24,25,26], Nicotiana tabacum [21,22,29], Solanum chacoense , Camellia japonica , Torenia fournieri  and Actinidia deliciosa  as well as angiosperm monocots like Lilium longiflorum [48,49] and Zea mays . More recent studies have focused on the gymnosperms like Pinus sylvestris , Picea meyeri  and several others [28,52].
One of the main differences between the primary cell wall of somatic and pollen tube cells is despite its presence, the low abundance of cellulose, a β-(1→4)-glucan. Instead, callose, a β-(1→3)-glucan, is the main cell wall polysaccharide. Callose is mostly localized in the inner cell wall and is absent from the tube tip of most angiosperm pollen tubes [53,54] including A. thaliana (Figure 2c) . In contrast, in Cycas and several Pinus species, callose was not detected in the pollen tube wall by aniline blue staining . However, in P. sylvestris, a strong fluorescence was detected with aniline blue at the tube tip . In addition, callose is deposited at periodic intervals to form callose plugs that maintain the tube cell in the apical expanding region of angiosperm pollen tubes (Figure 2c) and separates the viable from the degenerating region of the tube . In tobacco using CBH-I-gold and LAMP MAb  and in A. thaliana using CBM3a  and LAMP MAb , callose and cellulose are localized in the plugs and in the inner cell wall of the pollen tube. In contrast, in long-living and slow-growing gymnosperm pollen tubes, the callose plug deposition is apparently not a consistent feature as well as the permanent callose wall in pollen tubes . This observation suggests that in the evolution of flowering plants a permanent callose wall and callose plug deposition appeared through the short-lived and fast-growing pollen tubes of angiosperms . Cellulose is present in the entire cell wall of pollen tubes with a weaker staining with calcofluor white or CBH-I-gold labeling at the tip in most angiosperms [22,25,27,30]. Recently, Chebli et al.  using CBM3a that binds to crystalline cellulose found two populations of A. thaliana pollen tubes displaying intense or weak labeling at their tips suggesting that the labeling was related to temporal growth rate. Similarly, in T. fournieri, the distribution of cellulose changed temporally and spatially, being abundant in freshly germinated pollen tubes, and absent from the tube tip of older pollen tubes . Using atomic force microscopy, Wu et al.  also revealed that cellulose microfibrils were more abundant in the apical region of slow-growing tubes whereas only few microfibrils were observed in the auxin-stimulated pollen tubes suggesting a correlation between cellulose abundance and pollen tube growth. In Conifers, pollen tubes have cellulose in the entire cell wall and may contain more cellulose deposited at the tube tip, which may explain the slower growth [52,56].
Pectins are complex polymers consisting of homogalacturonan (HG), which can be methyl- and acetyl-esterified, rhamnogalacturonan-I (RG-I), rhamnogalacturonan-II (RG-II), and xylogalacturonan . HG is a polymer of repeated units of (1→4)-α-d-galacturonic acid. Upon block wise action of pectin methylesterases on methylesterified HG, several parallel HG chains can be cross-linked via the interaction of the negative charges of the carboxyl groups of galacturonic acid and calcium . RG-II has a galacturonan backbone with four well defined oligosaccharides composed of unusual sugars such as apiose, aceric acid and 3-deoxy-d-manno-2-octulosonic acid (Kdo) of unknown function . RG-II is present in the primary cell wall of all higher plants and its structure is evolutionarily conserved in the plant kingdom. In the cell wall, it exists predominantly in the form of a dimer that is cross-linked by a borate di-ester between two apiosyl residues . On the other hand, RG-I consists of the repeating disaccharide unit, (1→4)-α-d-galacturonic acid-(1→2)-α-l-rhamnose. On the rhamnosyl residues, a wide variety of side chains can be detected ranging from monomers to large oligosaccharides such as (1→4)-β-d-galactan, (1→5)-α-l-arabinan, and/or type I arabinogalactan .
Most of the studies on the pectic wall of the pollen tube focused on the detection of HG domains using the JIM5 and JIM7 mAbs (Table 1). To date, localization data of other pectic domains such as xylogalacturonan and RG-I side chains in the pollen tube wall are scarce. Immunofluorescence labeling of weakly and highly methylesterified HG with JIM5 and JIM7 or the newly introduced LM19 and LM20 depends clearly on the species, the in vitro growth condition and the growth rate of the pollen tube . It is however generally observed that in most angiosperms, highly methylesterified HG is mostly detected at the tip (Figure 2d) and weakly methylesterified HG epitopes are preferentially detected either in the entire pollen tube or in the pollen tube except in the tip region as shown in the Brassicacae (A. thaliana) , Solanaceae (wild potato, tobacco, petunia), Oleaceae (jasmine), Poaceae (corn) , Scrophulariaceae (T. fournieri)  and Liliaceae (lily) [48,49]. Similar observations were obtained in Picea meyeri  and Picea wilsonii  pollen tubes. In other gymnosperm species like P. macrophyllus and P. banksiana, pollen tubes were not labeled with JIM5 and JIM7 using electron microscopy observation .
Based on Elisa assays and dot-blots, it was clearly shown that JIM5 and JIM7 as well as LM19 and LM20 have specific but also overlapping binding capabilities to different degrees of methylesterification (DM) of HG domains after random or blockwise action of pectin methylesterases (PME) [37,62]. LM20 binds to HG with DM ranging between 85 and 16%, whereas LM19 binds to HG with DM between 66% and the demethylesterified form . Using these data and assuming that PME has a blockwise action to allow calcium cross-linking in the shank of the tube, we can estimate that the DM of HG at the tip is probably over 70% and back from the tip, the DM is less than 15%. In lily, this change of methylesterification level occurs between 15 and 20 µm from the pole of the pollen tube corresponding exactly to the transition zone between the apical dome and the cylindrical shank of the cell . In A. thaliana, this modification takes place closer to the tip (between 3 and 10 µm) . Recently, propidium iodide (PI) was used to probe low methylesterified HG on living A. thaliana and L. longiflorum pollen tubes, which allowed following the dynamics of the pectin during pollen tube growth. The fluorescence of PI was detected at the tip and the shank of the pollen tubes with PI fluorescence oscillations preceding growth rate oscillations . Finally, in certain species such as lily , Ornithogalum , tobacco  and others , periodic ring-like labeling patterns of weakly methylesterified HG were clearly visible along the pollen tube and originated from cell wall deposition during the slow growth pulses .
Side chains of RG-I are also present in the cell wall of pollen tubes. Using LM6 and/or LM13, epitopes associated with arabinan are evenly distributed along the entire pollen tube in A. thaliana , A. deliciosa  and P. wilsonii . At the electron microscopy level, arabinan is mostly detected in the outer cell wall layer in A. thaliana  consistent with the location of other pectic motifs such as HG. Galactan is also detected in A. thaliana pollen tubes but the labeling intensity is weak  and almost absent in Picea .
Xyloglucan (XyG) is the major hemicellulosic polysaccharide of the primary cell wall of angiosperm eudicots and non-commelinid monocots [64,65]. Classic XyG consists of a (1→4)-β-d-glucan backbone substituted with xylose, galactose-xylose or fucose-galactose-xylose motifs . In the primary cell wall, XyG interacts with cellulose via hydrogen bonds and participates in the control of cell expansion . The presence of fucosylated and galactosylated XyG was assessed only recently in A. thaliana pollen tubes using CCRC-M1 [25,68] and LM15 . Labeling with both mAbs is detected in the entire pollen tube wall and at the electron microscopy level; it was shown that XyG is present in the outer and inner layers of the pollen tube cell wall  suggesting a possible interaction with cellulose microfibrils.
All these data reveal a common organization of the pollen tube cell wall in the species from the angiosperm eudicots and the non-commelinid monocots. In contrast, with the slow-growing and short-traveling gymnosperm pollen tubes, it appears that the distribution of cell wall polymers, especially the callose, is altered . However, more studies using the probes listed in Table 1 are required to draw a general conclusion. To date, the investigation on the distribution of RG-II in pollen tubes is very limited but with the development of new specific probes for each individual side chains, the gap might be soon overcome. Another attracting method that may develop in the near future in the study of cell wall dynamics during pollen tube growth is the use of sugar analogs compatible to click chemistry associated with in vivo cell imaging . In this method, sugar analogs are metabolically incorporated into cell wall polymers and subsequently labeled with covalent linkages to fluorescent probes  as shown with alkynylated fucose analog incorporated in the pectin of A. thaliana root cell wall . This method will allow for insight into the dynamics and recycling of cell wall polymers on living pollen tubes.
2.2. Chemical Composition of Pollen Tube Cell Wall
Only very scarce studies have focused on the biochemical characterization of the pollen tube cell wall. The most striking point observed in the few biochemical characterizations of the cell wall of tobacco, C. japonica, lily, tulipa and A. thaliana pollen tubes is consistently the high level of arabinosyl residues [25,73,74]. In A. thaliana, Ara represents 43%, Glc 20%, GalA 11%, Gal 8% and Rha 5% of the total sugars . Linkage analyses show that most of the arabinosyl residues are T-Ara,5-linked and to a lesser extent 2,5-linked. These data indicate that the pectin of A. thaliana pollen tube cell wall is composed of 6% HG, 5% RG-I backbone harboring abundant chains of (1→5)-α-l-arabinan. This common feature suggests that arabinan may have an important role during pollen tube growth. Finally, linkage analyses also indicate (1) that most of the Glc is 3-linked indicating the abundance of callose [25,73] and (2) confirm that XyG is also present based on the detection of 4-Glc, 2-Xyl and T-Xyl, T-Gal and Fuc residues . According to the one letter code proposed by Fry et al. , the unsubtituted glucosyl residue of the backbone is represented by the letter G. X, L and F represent the substitution by xylose, galactose-xylose and fucose-galactose-xylose, respectively. XyG can also be O-acetylated generally on the galactose, indicated by an underline letter, but the biological significance of O-acetylation is not known yet . Generally, every four or five glucoses of the glucan backbone are not substituted allowing the cleavage of the polymer by endo-glucanase. The small oligosaccharides can then be analyzed by MALDI-TOF mass spectrometry, known as OLIMP method (OLIgosaccharide Mass Profiling) . Using this technique, the fine structure of A. thaliana pollen tube XyG was recently determined. It revealed significant differences with the XyG from vegetative organs such as leaves (Figure 3). Whereas XXXG is the main fragment of leaf XyG [25,78], the fucosylated and O-acetylated fragments (XXFG and XLFG) are the major motifs in A. thaliana pollen tube XyG  suggesting an important role of these two features in pollen tube growth and/or in the interaction with the female tissues.
Used in the mid-90s to study the cell wall composition of algae  and later widely adopted to screen flax and A. thaliana cell wall mutants [81,82], Fourier transform infrared (FT-IR) microspectrometry associated with principal component analysis was recently used to study the effect of hormones, minerals or drugs on the cell wall composition of elongating pollen tubes [51,83]. It shows that treatments of P. meyeri pollen grains with brefeldin A, a drug able to inhibit the secretory pathway, reduce the pollen germination and tube growth by disrupting the secretory vesicles at the tip and significantly decrease the content of pectin in the apical region . Treatments with nitric oxide donor or NO synthase inhibitor induce the accumulation of acidic HG and callose in the tip region . Interestingly, blocking the release of intracellular calcium with drugs significantly alters the cell wall structure in Picea pollen tubes with the accumulation of callose and the disappearance of methylesterified HG at the tube tip . Finally, treatment of T. fournieri pollen tubes with auxin promotes the growth by stimulating the synthesis of pectin, reducing the cellulose density and modifying the orientation of cellulose microfibrils as observed by atomic force microscopy . However, whereas the vibrations associated with cellulose, phenolics, the methylester and the carboxyl groups of GalA are well assigned by FT-IR, the technique does not allow discriminating clearly other pectin motifs such as arabinan and/or galactan side chains of RG-I in the cell wall network. It is, however, a non destructive method that may be convenient to use in the future for determining the overall composition of pollen tube cell wall mutants compared to wild type. It may also be useful to follow the evolution of the cell wall composition in different portions of the pollen tube during growth.
Due to the technical challenges involved such as the labor intensive work to collect enough material, the number of studies focused on the biochemistry of pollen tube cell wall is limited. As a consequence, it does not permit to assess clearly the differences in the cell wall composition between angiosperm (monocot and eudicot) and gymnosperm. However, with the development of more sensitive equipments such as mass spectrometry, more information may be soon collected.
3. Cell Wall Polymer Biosynthesis in Pollen Tubes
3.1. Pectin Biosynthesis
Pectin represents one of the main carbohydrate polymers found in the cell wall of pollen tubes. Given the complexity of its structure, it is predicted that 67 different glycosyltransferases, methyltransferases and acetyltransferases are required for its biosynthesis . The synthesis of the different pectin motifs is carried out in the Golgi apparatus and they are secreted via Golgi-derived vesicles .
The synthesis of HG requires the activity of GALACTURONOSYLTRANSFERASEs (GAUTs) that was biochemically demonstrated in Petunia axillaris pollen tubes . In A. thaliana, the multigenic family of GALACTURONOSYLTRANSFERASE (GAUTs) is composed of 15 genes [86,89] whose members are related to another family representing the GALACTURONOSYLTRANSFERASE-LIKE (GATLs), composed of 10 genes . GAUT1 (CAZy family GT8) is a galacturonosyltransferase gene that first was shown to be functionally implicated in the HG synthesis in A. thaliana vegetative organs . The inactivation of GAUT8 induces a reduction of the level of HG epitopes, a decrease of the amount of GalA in the cell wall of vegetative organs and a partial sterile phenotype . Among all these genes, 13 GAUTs and 8 GATLs are expressed in the inflorescence of A. thaliana [89,90]. According to transcriptomic data, only two GAUTs (GAUT13 and GAUT14) and two GATLs (GATL4 and GATL7) are expressed in pollen tubes [90,93]. Interestingly, the GALT4 expression seems to be pollen specific and is highly expressed in A. thaliana pollen tubes , which may suggest its implication in the synthesis of HG in pollen tubes but functional studies are necessary to assess the role of these genes in pollen tube growth.
In A. thaliana, the gene At5g33290 is involved in the xylogalacturonan biosynthesis, but the xgd1 (xylogalacturonan deficient1) mutants do not display any visible pollen or pollen tube phenotype . Other xylogalacturonan biosynthesis genes are undoubtedly implicated in this process but it remains to be established.
The backbone of RG-I is made of a repeating disaccharide α-(1→4)-d-GalA-α-(1→2)-l-Rha with Rha residues that can be substituted with galactan, arabinan and/or arabinogalactan . In the arabinan side chain, arabinosyl residues are almost entirely in the furanose configuration. Interestingly, rice REVERSIBLY GLYCOSYLATED PEPTIDEs (RGPs) show strong amino acid sequence identity (~80%) with an UDP-arabinopyranose mutase implicated in the interconversion of UDP-Arap and UDP-Araf . Moreover, in A. thaliana, double knock-out mutations in two RGPs (RGP1 and RGP2) showed a strong defect in the inner pollen wall and pollen lethality  suggesting that RGP1 and RGP2 act redundantly during pollen development. More recently, Rautengarten et al.  have shown that RGP1 and RGP2 are cytosolic and able to perform this interconversion indicating that RGPs may be part of the arabinan biosynthesis network. However, further studies are required to verify if RGP1 and RGP2 are also involved in the growth of pollen tubes. Moreover, biochemical evidence is needed to verify if the arabinan side chains of RG-I in the mutants are structurally different to the one found in wild type pollens and if other cell wall molecules containing Ara residues such as arabinogalactan proteins are not also affected.
Studies of the possible involvement of RG-II in pollen tube growth are very recent. In 2006, it was shown in tobacco that the mutation in NpGUT1 (Nicotiana plumbaginifolia GLUCURONOSYLTRANSFERASE1) resulted in the inhibition of pollen tube elongation, presumably due to an abnormal deposition of RG-II and boron in the pollen tube tip cell wall . However, it was shown recently that in A. thaliana, IRX10 (IRREGULAR XYLEM10) and IRX10-L (IRREGULAR XYLEM10-LIKE) proteins, which are closely related to NpGUT1, play a critical role in the synthesis of glucuronoxylan and not RG-II. [100,101]. To our knowledge, no report has shown any glucuronoxylan in the cell wall of A. thaliana or tobacco pollen tubes and these data contrast with the proposed function of NpGUT1 in the RG-II synthesis in pollen tubes.
Recently, three other genes involved in the biosynthesis of RG-II were shown to play an important role during A. thaliana pollen tube elongation. KDO-8-P SYNTHASEs (AtKDSA1 and AtKDSA2) are involved in the synthesis of Kdo, one of the rare sugars composing the RG-II, with eight carbons. Atkdsa1 and Atkdsa2 double pollen mutants in quartet background are unable to form an elongated pollen tube properly and to perform fertilization . In 2010, two male gametophyte defective (mgp) mutants, impaired in the biosynthesis of RG-II were isolated: mgp4, knock-out for a RG-II XYLOSYLTRANSFERASE  and mgp2, knock-out for a SIALYLTRANSFERASE-LIKE . Both mutants display similar phenotypes with a strong inhibition of pollen germination and a delayed pollen tube growth in vitro and in vivo compared to wild type. Because the three A. thaliana sialyltransferase-like proteins, homologous to mammalian sialyltransferases, do not show any sialyltransferase activity in vitro and that the nucleotide sugar donor of the sialyltransferase CMP-Sia is similar to CMP-Kdo, Deng et al.  suggested that these genes may be involved in the RG-II biosynthesis pathway. Another contribution pointing out the critical role of RG-II in pollen tube growth was recently brought by Kobayashi et al. . They studied the gene coding for the enzyme CTP:Kdo cytidylyltransferase (CMP:Kdo Synthetase, CKS) that activates Kdo as a nucleotide sugar during the biosynthesis of RG-II. They showed that the protein is located in the mitochondria and that this gene is essential for pollen tube development as the mutation in CKS induces the inhibition of pollen tube elongation . All these studies indicate that RG-II is important for pollen tube growth but none of the studies have shown biochemically that the RG-II structure in the pollen or the pollen tube was impaired. The development of specific probes targeting the different side chains of RG-II should facilitate studies on this non-abundant but important pectin motif in pollen tube growth but to date such tools are not available.
3.1.5. Pectin Methyltransferase and Pectin/XyG Acetyltransferase
The transferase activity of methyl and acetyl groups on HG was shown in vitro [106,107]. QUASIMODO2 and 3 (QUA2 and QUA3) are two genes coding for putative HG methyltransferases but their biochemical activities and their function during pollen tube growth have not been confirmed [108,109]. In 2011, a mutant designated as reduced wall acetylation2 (rwa2) was studied. The loss-of-function in the RWA2 gene was accompanied by a decrease of the level of acetylated cell wall polymers  but no phenotype was observed on the pollen tube indicating that other genes are likely to be involved in this process.
3.2. Xyloglucan Biosynthesis
Based on the structure of XyG, its biosynthesis requires a combination of (1→4)-β-glucan synthases, (1→6)-α-xylosyltransferases, (1→2)-β-galactosyltransferases, (1→2)-α-fucosyltransferases and O-acetyltransferases . In A. thaliana, CSL4 codes for a (1→4)-β-glucan synthase involved in the synthesis of the XyG backbone but transcriptomic data indicate that this gene is not expressed in pollen . At least five XYLOGLUCAN XYLOSYLTRANSFERASEs (XXTs) have been identified in A. thaliana [76,113,114] but their implications during pollen tube growth have not been assessed yet. Two XYLOGLUCAN GALACTOSYLTRANSFERASEs were also characterized: MUR3 in A. thaliana  and more recently XLT2 in Tropaeolum majus . However, none of these genes is expressed in pollen grains or pollen tubes . MUR1 codes for an enzyme that catalyzes the first step of the biosynthesis of GDP-fucose and the mur1 mutants show a lack of labeling of fucosylated XyG epitopes with CCRC-M1 in hypocotyls, shoots or leaves . However, the mutation does not affect the distribution of the fucosylated XyG epitopes in the pollen tube suggesting that this gene is not implicated in the XyG biosynthesis in pollen tubes. Mutation in the FUCOSYLTRANSFERASE gene (FUT1, FT1 or MUR2) eliminates the fucosyl residues on the XyG side chains in all major plant organs indicating that FUT1 is involved in most of the XyG fucosyltransferase activity in A. thaliana [117,118]. MUR1 and FUT1 are not expressed in pollen grains or pollen tubes but are strongly expressed in the stigma and in ovarian tissues in A. thaliana  suggesting that XyG from the female tissues may be highly fucosylated but more direct experimental evidence is required.
3.3. Cellulose Biosynthesis
It is generally assumed that cellulose microfibrils are assembled by cellulose synthases (CESs) located at the plasma membrane in a form of rosette terminal complex. However, the possibility that the first step of cellulose biosynthesis begins in the Golgi apparatus in higher plants cannot be ruled out . Different multigenic families are implicated in cellulose biosynthesis. Ten CESA (CELLULOSE SYNTHASE A) genes were found in the A. thaliana genome and it was shown by mutant analyses that they play distinct roles in the cellulose synthesis process [120,121]. Another multigenic family, CSLD (CELLULOSE SYNTHASE LIKE-D), related to CESA, seems also to be involved in cellulose biosynthesis and contains six members in the A. thaliana genome [122,123]. In rice, the genome contains 7 CESA and 5 CSLD genes . In tobacco, NaCSLD1 (Nicotiana alata CELLULOSE SYNTHASE-LIKE D1) was found to be only expressed in the anther and in vitro-grown pollen tubes and was predicted to code for a cellulose synthase in pollen . In N. tabacum pollen tubes, CESA and CSLD were detected along the entire length of the pollen tubes with a higher concentration at the apex . Similarly, in A. thaliana, CESA6, CSLD1 and CSLD4 were found at the plasma membrane of the pollen tube both at the tip and in the shank [26,127]. Moreover, crystalline cellulose was also found inside cytoplasmic vesicles and the trans Golgi network in A. thaliana pollen tubes leading to the hypothesis that the synthesis of short cellulose microfibrils may initiate in this compartment giving the pollen tubes the head start in assembling the cell wall necessary to promote rapid elongation . Alternatively, the vesicles containing the cellulose may originate from endocytosis suggesting that cellulose in the shank of the tube may be degraded and recycled .
The CESA1 and CESA3 mutations are both gametophytic lethal. 50% of pollen grains from the heterozygous cesa1+/− or cesa3+/− plants are significantly deformed and do not produce pollen tube . The cesa6 null mutants display subtle growth defect and the pollen is not deformed . On the other hand, the triple cesa2/6/9 mutants are sterile and pollen grains are strongly deformed . The data indicates that CESA2 is functionally redundant with CESA6. As CESA9 is strongly expressed in pollen grains, these studies suggest that CESA1, 3, 6 and 9 play a critical role during pollen grain formation. Recently, it was shown using pCESA6::GFP-CESA6 construction that CESA6 is expressed in pollen tubes indicating that in addition to CESA1, 3 and 9, CESA6 may also play a role during pollen tube growth .
Three genes from the CSLD family are also implicated in pollen tube growth. Csld1 and csld4 homozygous mutants are sterile. Mutant pollen grains show abnormal germination and reduce pollen tube growth in vitro and in vivo. In addition, high level of pollen tubes is bursting due to a reduced cellulose content, abnormal callose deposition and thickened and highly irregular cell wall [123,127]. Finally, mutation in CSLC6 results in a strong reduction of pollen tube growth . All these data support the fact that despite the low abundance of cellulose in the cell wall of pollen tubes, it has an important function in maintaining the integrity of the tube cell.
3.4. Callose Biosynthesis
Callose is also synthesized at the plasma membrane by callose synthases (CALSs) located at the apex and the distal regions of tobacco pollen tubes. In longer pollen tubes, CALS accumulates also close to the callose plug . Twelve putative CALS genes (CALS1-12) have been identified in the A. thaliana genome . Among these 12 genes, CALS5 is implicated in the normal deposition and patterning of the exine pollen grain [131,132] but opposite data are obtained concerning the pollen viability and the ability of the pollen tube to grow normally. NaGSL1 (Nicotiana alata GLUCAN SYNTHASE-LIKE1) was shown to be a callose synthase  involved in the control of callose synthesis during pollen tube growth . In 2011, a study brought evidence that CALS5 orthologues are expressed in pollen grains of many different angiosperms and gymnosperms but CALS5 was only expressed in fast-growing pollen tubes (i.e., angiosperms), suggesting that CALS5 plays different but crucial roles during pollen formation and/or germination and pollen tube growth . This study also supports the reports showing that the callose wall in slow-growing pollen tubes is generally transiently detected and the callose plug has so far not been observed in gymnosperm pollen tubes. Based on such variability and transient expression of callose in the pollen of Pinus, Pacini et al.  suggested that the callose may not have a structural function but rather serves as a reserve polysaccharide. In contrast, in fast growing pollen tubes like in S. chacoense and Lilium orientalis, callose was shown to have an important mechanical function .
4. Cell Wall Remodeling during Pollen Tube Growth
4.1. Cell Expansion: Xyloglucan-Cellulose Reassembly
Expansins were first discovered in cucumber hypocotyls  and oat coleoptiles . According to Sampedro and Cosgrove , expansins belong to a superfamily composed of four families: (1) EXPANSIN A (EXPA), also called α-expansin; (2) EXPANSIN B (EXPB), also known as β-expansin; (3) EXPANSIN-LIKE (EXLA); and (4) EXPANSIN-LIKE B (EXLB). α- and β-expansins are involved in cell expansion: EXPAs may promote separation of cellulose microfibrils by inducing local dissociation and slippage of XyG on the surface of the cellulose, whereas EXPBs work on different polymers, maybe xylan, with a similar effect . The precise role of EXLA and EXLB has not been has not been established yet  and to date, no enzymatic activity has been detected for these proteins [140,141].
The A. thaliana genome contains 36 genes encoding putative EXPs [141,142]. Expression profile analyses of the transcripts reveal that two expansin genes one α-(EXPA4) and one β-(EXPB5) are strongly expressed in dry pollen grains, during pollen imbibition and pollen tube growth (Table 2). In addition, four other EXPs are strongly expressed in the stigma and one in the ovary of A. thaliana (Table 2). To date and to our knowledge, no study has pointed out the role of expansins in the remodeling of the pollen tube cell wall in eudicot plants. Most of the work on expansins comes from the Poales in which the development of pollen grains is accompanied by the expression of EXPB. In rice, several putative EXPBs were found in pollen grains by proteomics approach  and 4 isoforms were purified from the maize pollen . During the maturation of wheat and triticale male gametophytes, a strong expression of two EXPB genes is detected but unlike the β-expansins from maize, they are not expressed in the mature pollen [145,146]. Even if the exact function of pollen EXPBs remains unanswered, Cosgrove et al.  suggested that they are released from the pollen grain on the pistil to soften the cell wall of the stigma thus facilitating the penetration and the growth of the pollen tube. Some others hypothesized that EXPBs are implicated in the formation of the exine wall during the male gametophyte formation .
|Cell wall metabolism||Locus||Protein name||Expression level|
|Pollen grain||Pollen tube||Pistil|
|Dry||Imbibed||4 h in vitro||Semi in vivo||stigma||ovary|
|CBMs||At1g20190||Expansin A11 (EXPA11)||<50||<50||<50||<50||1,614.7||421.6|
|At1g26770||Expansin A10 (EXPA10)||<50||<50||<50||<50||1,893.9||641.8|
|At2g28950||Expansin A6 (EXPA6)||<50||<50||<50||<50||1,919.8||1,614.2|
|At2g39700||Expansin A4 (EXPA4)||4,069.6||3,962.1||3,950.8||2,106.8||321.3||429.6|
|At3g45970||Expansin-like A1 (EXLA1)||<50||<50||<50||<50||1,462.7||322.1|
|At3g60570||Expansin B5 (EXPB5)||1,020.2||1,139.5||1,347.1||3,002.9||53.9||52.7|
CBMs. Carbohydrate-Binding Modules, GH. Glycoside hydrolase, XTH. Xyloglucan endo-transglucosylase hydrolase.
4.1.2. Xyloglucan endo-Transglucosylase Hydrolase
The two known activities of XyG endo-transglucosylase hydrolase proteins (XTHs) are XyG endo-transglucosylase (XET) and XyG endo-hydrolase (XEH) . The XET activity consists of cleaving XyG polymers and joining the newly generated end to another XyG chain whereas XEH activity hydrolyzed XyG polymers . XET activity was detected in extracts of the growing portions of various eudicots (including pea, lupin, tomato, sycamore, cow parsley, dandelion and bean), monocots (chive, maize, brome grass and Yorkshire fog) and Bryophytes (liverwort and moss) [153,154]. XTHs are believed to play a central role in the construction and the disassembly of the cell wall architecture . XTHs are encoded by large gene families in land plants and A. thaliana and rice contain 33 and 29 XTH genes dispersed across their genomes, respectively [155,156]. Among the 33 XTHs in the A. thaliana genome, 4 are strongly expressed in flowers. Becnel et al.  have studied the expression of the XTH genes using XTH::GUS constructions and they showed that pXTH29::GUS and pXTH30::GUS activities are clearly detected during the anther development and in the mature pollen grain . In contrast, pXTH1::GUS and pXTH33::GUS activities are restricted to very young flowers. Microarray data extracted from EFP browser are consistent with these results (Table 2). Moreover, expression profiles of XTH29 and XTH30 appear to be pollen specific suggesting a specialized function during pollen development.
However, to date, no evidence demonstrates a role of XTHs in the pollen tube growth and cell wall remodeling. Only one XTH was linked to pollination. The loss of function of AtXTH28 led to a dramatic decrease in seed setting due to the inability of the plants to self-pollinate. This phenotype was caused by a net reduction of the stamen filament length due presumably to a reduced capability of the filament cells to expand .
4.2. Pectin Methylesterase and Pectin/Xyloglucan Acetylesterase
HG is synthesized in the Golgi apparatus and deposited in the expanding tube tip in a highly methylesterified form . The methylesterified HG in the apical zone is thought to provide sufficient plasticity for sustaining the pollen tube growth . Upon block-wise action of PMEs, de-methylesterified HG polymers can form multimers via ionic bonds between the negatively charged carboxyl groups of several HG and Ca2+ ions forming a pectate gel that may provide rigidification of the pollen tube cell wall [12,58]. Therefore, the control of the cell wall plasticity by PMEs is critical to ensure a proper fertilization. Conversely, upon random action of PMEs, the partial removal of methylester groups may allow the pectin-degrading enzymes, polygalacturonases (PGs) or pectate lyases (PLs) (see lower section) to cleave the HG backbone thus affecting the rigidity of the cell wall [58,160]. This sequential action of PME and PG was demonstrated in the quartet mutants that release pollen grains as tetrads due to the persistence of pectic polysaccharides . The QUARTET1 gene encodes a PME that is required in association with the QUARTET3 encoding a PG for the degradation of the HG of the tetrad resulting in the normal pollen separation during microsporogenesis [162,163].
The A. thaliana genome contains 66 putative PMEs. Most of the genes encoding PMEs display a tissue-specific expression pattern, especially for 14 of them that are specifically expressed in pollen grains or pollen tubes (Table 3) [93,164]. Moreover, proteomics studies of germinated pollen grains from maize, wheat, rice and A. thaliana have identified two putative PMEs in germinated maize pollen , one in rice  and at least one in A. thaliana pollen tubes . In tobacco pollen tubes, biochemical analyses have shown the presence of seven isoforms with a wide isoelectric point range . Two PME isoforms were co-localized with methylesterified HG in the cell wall and Golgi-derived vesicles suggesting that PMEs are transported to the tip under an inactive precursor form .
The first functional characterization of PME genes and their critical roles in pollen tube growth were obtained from two knock-out mutants vanguard1(vgd1)  and atppme1 . The disruption of VGD1 resulted in the burst of pollen tubes in vitro and marked retardation of the vgd1 pollen tube elongation in the pistil resulting in a strong reduction of male fertility and seed set . The lack of AtPPME1 activity in knock-out mutants affects the shape and the growth rates of the pollen tubes, indicating that AtPPME1 is required for the integrity of the cell wall and for the tip-polarized growth . Moreover, when PME from orange peel is exogenously applied to pollen tubes of Lilium formosanum and tobacco or when PME is overexpressed, the pollen tube growth is inhibited .
|Cell wall metabolism||Locus||Protein name||Expression level|
|Pollen grain||Pollen tube||Pistil|
|Dry||Imbibed||4 h in vitro||Semi in vivo||stigma||ovary|
CE. Carbohydrate Esterases, PAE. Pectin AcetylEsterase, PME. Pectin MethylEsterase, PPME. Pollen Pectin MethylEsterase, VGD. Vanguard, VGDH. Vanguard Homolog.
The main regulators of PMEs are PME inhibitors (PMEIs). Sequence analyses indicate that several PMEs contain, in addition to the catalytic domain, an N-terminal extension domain (the PRO region) showing similarity with PMEI domains . Based on this, PMEs are classified in two distinct groups depending on the presence or absence of this putative PMEI domain. Group 1 PMEs do not have the PRO region, whereas PMEs from group 2 can contain from 1 to 3 PMEI domains . It is hypothesized that the PRO region is cleaved during the maturation of PME, as so far, only PMEs lacking this domain were found in the cell wall .
Recently, Wolf et al.  indicated that the PRO region of the group 2 PMEs might regulate the release of the mature PMEs from the Golgi apparatus. It was also suggested that the PRO region might play an auto-inhibitory role during maturation . PMEIs are not only found in the PRO region of PMEs but also exist as individual proteins sharing strong sequence similarities with invertase inhibitors (Inv inhibitors). However, there is no clear evidence of a similar function and mode of action between PMEIs/Inv inhibitors and PMEI domains of PMEs. The A. thaliana genome contains 76 genes coding highly putative PMEIs/Inv inhibitors. The expression patterns of PMEIs/Inv inhibitors are all regulated in a tissue-specific manner [171,172] and transcriptomic data reveal that PMEIs/Inv inhibitors are highly expressed in the A. thaliana pollen compared to other tissues [171,173]. As 9 out of the 14 PMEs specifically expressed in pollens are from the group 2 (with PMEI domains), it may suggest that PMEIs play a crucial role in regulating the activity of PMEs during pollen germination and pollen tube growth. Suppression of the expression of At1g10770 (coding for a putative PMEI) leads to a partial male sterility reducing the seed set by inhibition of pollen tube growth . Moreover, treatments of pollen tubes with exogeneous PMEI also result in an abnormal germination and burst of pollen tubes in A. thaliana . Finally, it was shown that AtPPME1 and AtPMEI2, both pollen specific, physically interact and in vitro assays revealed that AtPMEI2 was able to inactivate AtPPME1 . The transient expression of AtPPME1 and AtPMEI2 in tobacco pollen tubes demonstrated that AtPPME1 accumulates uniformly from the tip to the shank of the pollen tube. In contrast, the localization of AtPMEI2 is restricted to the tip and in endosomal vesicles suggesting its internalization and recycling . PMEs are thought to play an important role during the tip-polarized growth of the pollen tube by controlling the mechanistic properties of the cell wall. However, the function of PMEs is probably not restricted to the change of the mechanical properties of the cell wall. Weakly methylesterified HG have been implicated in other important physiological processes such as cell attachment in vegetative cells or organs [92,177,178] and in lily, associated with a stigma/style cysteine-rich adhesin (SCA), a secreted plant lipid transfer protein (LTP), in pollen tube adhesion [179,180]. Several LTPs are expressed in the transmitting tract of the A. thaliana pistil along the pollen tube path  that may be involved in this process. In tobacco, it was shown that TobLTP2 purified from the stigma exudates accumulate in the pistil and are able, as expansins do, to promote cell wall loosening. However, the pollen tube growth in LTP-silenced plants is similar to wild type plants, suggesting either that pollen tubes do not require this loosening protein or that other loosening agents may have act redundantly . Recently, LTP5, produced in A. thaliana pollen tubes and in the transmitting tract, was proposed to play important roles in maintaining the cell polarity at the tube tip and adhesion-mediated guidance perhaps by interactions with pectins . Direct evidence is lacking, but it appears highly probable that PMEs, by modifying the degree of methylesterification of HG, play a direct role in adhesion and guidance of the pollen tube.
Finally, one putative pectin acetylesterase was detected in rice pollen  and a recent report has shown that the overexpression of the Populus PECTIN-ACETYLESTERASE1 in tobacco affected the shape of the pollen grains and their abilities to germinate .
4.3. Pectin lyase
PL (PECTIN LYASE) and PLL (PECTIN LYASE-LIKE) genes are also abundantly expressed in tomato, tobacco, alfalfa and arabidopsis pollen [185,186,187] and several pollen allergens have PLL activities . Out of the 26 PLL genes, 14 are expressed in pollen . None of these 14 genes is specifically dedicated to the male gametophyte but 4 of them are strongly expressed in pollen grains (Table 4). To our knowledge, there is no experimental evidence of the implication of PLL in the remodeling of the pollen tube wall. Many promoter activities of the PLLs genes are similar to those exhibited by many POLYGALACTURONASEs (PGs) . This may imply a close functional association between PLLs and PGs, particularly in the digestion of the pollen grain cell wall prior to germination and during pollen tube growth [190,191].
|Cell wall metabolism||Locus||Protein name||Expression level|
|Pollen grain||Pollen tube||Pistil|
|Dry||Imbibed||4 h in vitro||Semi in vivo||stigma||ovary|
|PL1||At1g04680||Probable pectate lyase 1||<50||<50||<50||<50||681.0||1,457.2|
|At1g14420||Probable pectate lyase 3||3,922.2||3,514.5||3,591.2||1,171.3||<50||<50|
|At2g02720||Probable pectate lyase 6||3,608.0||3,599.7||3,533.1||4,007.9||<50||<50|
|At3g01270||Probable pectate lyase 7||6,694.0||6,572.3||6,546.1||7,161.1||166.1||112.7|
|At4g24780||Probable pectate lyase 18||<50||<50||<50||<50||1,969.1||1,173.3|
|At5g09280||Major pollen allergen like protein||<50||<50||<50||3,192.1||<50||<50|
|At5g15110||Probable pectate lyase 18||3,865.4||3,782.2||3,390.4||625.1||<50||<50|
PL. Pectin Lyase.
4.4. Glycoside Hydrolases
Glycoside hydrolases (GHs) are enzymes that catalyze the hydrolysis of glycosidic linkages between two or more glycosides or between a carbohydrate and a non-carbohydrate moiety. In 1991, GHs were classified into 35 families  and to date they are divided into over 100 families . GHs involved in the reassembly of the pollen tube cell wall belong to the GH3, 9, 10, 17, 28, 35, 43 and 51 families. Their activities as well as their possible functions during pollen tube growth are presented in Table 5.
|Family||Known activities||Possible function during pollen tube growth|
|GH3||β-d-xylosidase (EC 18.104.22.168)|
α-l-arabinofuranosidase (EC 22.214.171.124)
β-glucosidase (EC 126.96.36.199)
|Degradation of xylan/arabinoxylan|
Degradation of RG-I, arabinogalactan proteins.
|GH9||Endo-(1→4)-β-glucanase (EC 188.8.131.52)|
Cellobiohydrolase (EC 184.108.40.206)
β-glucosidase (EC 220.127.116.11)
|Degradation of cellulose and XyG backbone|
May control the diameter of the pollen tube.
May help to digest the cell wall of the stigma to facilitate the pollen tube penetration in the female tissues.
|GH10||Endo-(1→4)-β-xylanase (EC 18.104.22.168)||Degradation of xylan|
|GH17||Endo-Glucan (1→3)-β-glucosidase (EC 22.214.171.124)|
Glucan (1→3)-β-glucosidase (EC 126.96.36.199)
Endo-(1→3-1→4)-β-glucanase (EC 188.8.131.52)
β-(1→3)-glucanosyltransglycosylase (EC 2.4.1.)
|Degradation of callose or β-mixed-(1→3, 1→4) glucans.|
May promote pollen germination and control the mechanical properties of the pollen tube cell wall during elongation.
|GH28||Polygalacturonase (EC 184.108.40.206)|
Exo-polygalacturonase (EC 220.127.116.11)
Exo-polygalacturonosidase (EC 18.104.22.168)
Rhamnogalacturonase (EC 22.214.171.124)
Rhamnogalacturonan α-l-rhamnopyranohydrolase (EC 126.96.36.199)
Endo-xylogalacturonan hydrolase (EC 3.2.1.-)
|Degradation of weakly esterified HG: cell wall loosening.|
May control the stiffness of the tube during elongation and/or help to digest the cell wall of the stigma thus facilitating the penetration of the tube.
Degradation of RG-I backbone
Degradation of xylogalacturonan
|GH31||α-xylosidase (EC 188.8.131.52)||Degradation of XyG or RG-II side chains|
|GH35||β-galactosidase (EC 184.108.40.206)|
Exo-β-(1→4)-galactanase (EC 3.2.1.-)
|Degradation of RG-I, XyG and/or arabinogalactan proteins.|
Turn over of pollen tube cell wall. Pollen tube guidance
|GH43||β-d-xylosidase (EC 220.127.116.11)|
α-l-arabinofuranosidase (EC 18.104.22.168)
|Degradation of xylan/arabinoxylan|
Degradation of RG-I, arabinogalactan proteins, arabinoxylan.
|GH51||α-l-arabinofuranosidase (EC 22.214.171.124)||Degradation of RG-I, arabinogalactan proteins, arabinoxylan.|
Endo-(1→4)-β-glucanases and endo-(1→3)-β-glucosidases are members of the GH9 and GH17 families, respectively (Table 5, Table 6). In A. thaliana, 25 genes are encoding GH9 proteins and 49 the GH17 proteins. Among the 25 putative CELLULASES, two are strongly expressed in pollen grains and three in in vitro-grown pollen tubes (Table 6). Four members of the GH17 family are expressed in in vitro-grown pollen tubes (Table 6). Three and five genes encoding the GH9 and GH17 are also found in the pistil tissues, respectively. Twenty years ago, these two enzyme activities were assayed in pistils and anthers of bean and they were linked to the cell wall disruption occurring during the release of the pollen grain from the anther and during the penetration of the pollen tube through the stigma . Recently, and despite its low abundance in the pollen tube cell wall, it was shown that cellulose plays a crucial role by influencing the diameter of in vitro-grown pollen tubes . As described previously, the cell wall of fast-growing pollen tubes is enriched in callose and several studies have shown that moderate β-(1→3)-glucanase treatments are able to stimulate the germination of pollen grains [53,196]. Moreover, it was reported that exo-β-glucanases might play an important role in the regulation of pollen tube elongation in lily . On the contrary, treatments with inhibitors of glucosidases severely inhibited the growth of pollen tubes . It was hypothesized that the mechanical properties of callose and more precisely the resistance to lateral deformation of the tube was regulated by glucanases  (Table 5).
|Cell wall metabolism||Locus||Protein name||Expression level|
|Pollen grain||Pollen tube||Pistil|
|Dry||Imbibed||4 h in vitro||Semi in vivo||stigma||ovary|
|GH10||At4g33850||GH 10 protein||1,571.9||1,369.8||1,495.2||205.7||<50||<50|
|At4g33860||Endo-(1→4)-β xylanase, putative||1,571.9||1,369.8||1,495.2||205.7||<50||<50|
|At5g42100||Glucan endo-(1→3)-β-glucosidase 10||<50||<50||<50||<50||726.5||1,402.3|
GH. Glycoside Hydrolases, CEL. Cellulase, RSW.Radially Swollen, KOR. Korrigan, PGA. Polygalacturonase, BGAL. β-galactosidase, XYL. xylosidase.
Polygalacturonases (PGs) are involved in the HG degradation. They were characterized in the pollen from corn and other Poales  and have since been identified in various plants including rice, pea, tomato and arabidopsis [143,190,201,202]. PGs belong to the GH28 family composed of 69 genes in A. thaliana [203,204]. In 2000, Torki et al.  showed that 7 PG genes were strongly expressed in A. thaliana flowers. Publicly available microarray data are consistent with this result as 6 PG genes are strongly expressed in pollen tubes and one is expressed in the pistil (Table 6). Together with the strong expression of more than 10 PMEs and 4 PLLs in pollen tubes, these data suggest an important remodeling of the HG during pollen tube growth. PGs are involved, during pollen maturation of Brassica campestris, in the intine and/or exine formations [206,207] and in Turnera subulata, PGs are implicated in self-incompatibility . PGs are released upon rehydration of triticale pollen grains  and are also detected in the tip region of pollen tubes in Brassica napus during papillar cell penetration  suggesting that PGs are probably involved in the loosening of the stigma cell wall during pollination. As PGs degrade weakly methylesterified HG and that the demethylesterification of methylesterified HG by PMEs at the tip of the tube is accompanied by the release of protons, it was suggested that this local change of pH in the pollen tube cell wall may promote PG activity [58,210]. This activation of PGs might then control the loosening of the pollen tube cell wall back from the tip and then promote the proper pulse growth of the tube (Table 5). Alternatively, pollen tube PGs may also affect the loosening of the stigma and transmitting tract cell wall to facilitate the penetration of the pollen tube (Table 5).
β-galactosidases (BGALs) belong to the GH35 family. BGALs can act on different substrates including arabinogalactan proteins, galactolipids, RG-I and RG-II side chains of pectin and XyG releasing galactose . Eighteen genes are encoding BGALs in the A. thaliana genome and the functional genomics analysis reveals that BGAL expression levels are high in mature leaf, root, flower and silique but are low in young seedling . Publicly available microarray data (Table 6) show that 2 BGALs are highly expressed in mature pollen grains and 2 others are highly expressed in the pistil confirming the results obtained by Ahn et al. . Other BGAL genes are also strongly expressed during the microspore mitosis in developing pollen grains . In rice, 35 genes are encoding BGALs; among them, two are strongly expressed in dry pollen grains  (Table 6). As mutants defective in BGAL have impaired fertility, it was hypothesized that BGAL may be involved in the pollen tube wall turnover in Brassica campestris by hydrolyzing arabinogalactan . In 1995, it was suggested in tobacco that BGALs could be secreted from the pollen tube and released in the stylar transmitting tract to modify the branching pattern of arabinogalactan involved in the guidance of pollen tubes [215,216]. In tobacco, BGAL mRNAs are accumulated during the formation of pollen grains, presumably stored for future use during pollen germination and pollen tube growth as BGAL activities were detected in growing pollen tubes . In rice, 6 isoforms of putative BGALs were detected by proteomic . Finally, it was also suggested that BGALs might also be required for PME activity [218,219]. Transcriptomic data showed very strong pollen specific expression profile of one β-xylosidase gene in mature dry pollen grains , and in in vitro and semi-in vivo grown pollen tubes. The exact substrate of this enzyme is not known but it may degrade several cell wall polymers such as xylan, xylogalacturonan and possibly N-linked glycoproteins. All the other putative xylosidases (12 genes that belong to the families GH3 and GH31) are only expressed in the pistil (Table 6). In addition, transcriptomic data do not show a strong expression of arabinofuranosidase genes in the pollen (Table 6). This is somehow surprising considering that Ara is one of the main carbohydrates present in the cell wall of A. thaliana pollen tubes . It may suggest that the Ara containing polymers are not remodeled and/or that arabinofuranosidases originate from the female tissues (Table 6). The pattern of expression of α-xylosidase genes (GH31) is close to the one found for the arabinofuranosidase genes. α-xylosidase genes are not strongly expressed in dry pollen grains or pollen tubes. However, two α-xylosidase genes are expressed in the pistil (Table 6). Analyses of the A. thaliana Atxyl1 mutants show reduced α-xylosidase activity, altered XyG composition and shorter siliques compared to the wild type. Moreover pAtxyl1::GUS expression is strong in the style . It suggests that AtXYL1 may remodel the XyG of pollen tubes. However, it is difficult to directly implicate this α-xylosidase activity in pollen tube growth as seed production was apparently not affected.
By comparing the proteome of rice pollen grains and pollen tubes, Dai et al.  showed that several proteins involved in the cell wall biosynthesis and remodeling are either up- or down-regulated. Several RGP, PME, PG and EXPB isoforms are up-regulated upon pollen germination whereas others PGs, xylanases and EXPBs are down-regulated indicating that several proteins are dedicated to pollen germination and others to pollen tube growth. The authors suggested that the down-regulated proteins in the pollen tube may result from their release into the culture medium. In the in vivo context, the release of these proteins in the pistil tissues may facilitate the pollen tube growth. Finally, glycosylated and/or phosphorylated proteins were detected and contributed to the generation of new isoforms . The activity of enzymes is commonly regulated by phosphorylation, glycosylation and/or interaction with specific inhibitors but more studies are required to assess the fine tuning and the exact function of these posttranslational modifications in pollen tube growth .
5. Mechanical Properties of the Cell Wall Network during Pollen Tube Growth
In recent years, A. Geitmann’s lab has studied the mechanical properties of pollen tubes using micro-indentation and finite element technique . In A. thaliana, lily and S. chacoense, it is observed that the tip region is elastic and the shank of the tube is rigid [26,53]. The modification of the cell wall mechanical properties using exogenous and moderate pectinase concentrations promotes pollen tube growth and the overall stiffness of the pollen tube decreased in both the apical and distal regions  suggesting that pectins are important components in respect to the cell wall mechanics . As expected, an increase of the pectinase concentrations results at first by in apical swelling and ultimately bursting of the pollen tube. By contrast, PME treatments of pollen tubes increase the cellular stiffness at the apex and reduce the visco-elasticity. It reveals that the gradient from methylesterified (in the hemisphere-shape tip) to de-methylesterified (in the cylindrical shank) HG increases the cell wall rigidity  by promoting calcium cross-links with the negatively charged carboxylic groups of HG. This was also observed by Rounds et al.  using PI on pollen tubes treated with PME. A dramatic increase of the PI fluorescence at the apex of treated pollen tubes was detected due to an increase of demethylesterified HG. The authors suggested that PI interacted with demethylesterified HG by competing with calcium.
Despite its low abundance, cellulose plays an important role in stabilizing the pollen tube tip wall especially in the transition zone between the tip and the shank . Cellulose microfibrils display an oblique orientation along the pollen tube wall in Pinus  whereas a more longitudinal orientation is observed in Lilium, S. chacoense and A. thaliana suggesting that cellulose microfibrils are not the main stress bearing component against turgor pressure [26,195,221]. However, cellulose is of main importance in the mechanical stabilization of the tip region. Cellulase treatments or inhibition of cellulose crystal formation with drugs resulted in larger pollen tube diameters and promoted tip swelling and eventually bursting  as observed with the cellulose synthase mutants. Similar phenotypes were observed on Petunia and lily pollen tubes treated with 2,6-dichlorobenzonitrile (DCB), a cellulose biosynthesis inhibitor  or on conifer pollen tubes treated with isoxaben . Recently, Derksen et al.  have shown that the cell wall structure of tobacco pollen tubes is organized both at the tip and back from the tip of 40–50 nm spaced lattice of continuous fibers that will allow intake of substantial size molecules from the surroundings.
In planta, XyGs are known to interact by hydrogen bounding with cellulose microfibrils but no information is available in pollen tubes. O-acetyl groups and the fucose residues of XyG do not seem to play a major role in the interaction with cellulose. In vitro experiments have shown that acetylated or de-acetylated XyG can cross-link similarly cellulose microfibrils . In contrast, the presence of galactosyl residues appeared to be important in promoting the interaction with cellulose. XyG lacking Gal residues self-associated and did not interacted with cellulose . Moreover, A. thaliana mutants with XyG lacking xylosyl and galactosyl residues showed a reduction of the tensile strength  and abnormal bulging in root hairs, possibly due to impaired cellulose-XyG assembly [225,226]. All together, these data suggests that the high levels of fucosylation and O-acetylation in the A. thaliana pollen tube XyG and perhaps in other species may prevent a strong interaction with cellulose microfibrils at the tip, promoting the fast growth of the pollen tube. Moreover, the high level of O-acetylation in XyG pollen tubes may also modulate the interaction between cell wall polymers and/or hinder enzymatic degradation  perhaps from enzymes originating from the pistil. Very recently, in root hairs of A. thaliana, a new branching pattern of XyG was characterized with GalA residues instead of Gal . This motif was not detected in A. thaliana pollen tubes but it indicates clearly that tip-polarized cells can have specific XyG compositions to modulate the interaction with cellulose microfibrils and promote fast growth.
The amorphous callose is also important in the mechanical properties of the pollen tube cell wall. Treatments of pollen tubes with lyticase, an enzyme able to degrade callose, increase the diameter of the pollen tube, reduce the cellular stiffness and increase the cellular viscoelasticity in the distal part of S. chacoense pollen tubes suggesting that the callose wall may function in resistance to compression and/or tension stresses . Using a combination of PME, pectinase and lyticase on fixed pollen tubes, Chebli et al.  suggested that cellulose and pectin are closely linked in the tip region of A. thaliana pollen tubes as demonstrated in the A. thaliana primary cell wall  and in the shank of the tube, a tight network of cellulose and callose is formed. Recently, using cellular force microscopy on lily pollen tubes, Vogler et al.  revealed also that the apparent stiffness of the pollen tube was lower at the tip than in the shank. However, they suggested that these differences are not originating from the distribution of the cell wall polymers or the thickness of the cell wall but solely due to the geometry of the pollen tube.
Over the last 25 years, the use of in vitro systems has been very valuable and a lot of information was collected concerning the distribution of the cell wall polymers in many species, but mostly focused on HG, callose, cellulose and arabinogalactan-proteins. In A. thaliana, functional genomics approaches have allowed the characterization of several genes implicated in the biosynthesis of pollen tube cell wall polysaccharides (mostly callose and cellulose). However, considering the large number of genes necessary to synthesize pectin, very few of them have been functionally characterized (several in the RG-II biosynthesis) and so far, none involved in the synthesis of XyG. Similarly, very few pollen genes involved in the remodeling of the pollen tube cell wall have been experimentally characterized. In addition, in the in vitro studies of pollen mutants, it is sometimes difficult to compare the data due to the use of different culture media and conditions, which may enhance or reduce the observed phenotypes. In many cases, a mutation completely inhibits pollen germination thus preventing the investigation of functional studies during pollen tube growth. Moreover, very little information is available on “non model” pollen tube species especially in gymnosperms and monocots. However, in recent years, the number of sequenced genomes from evolutionary divergent species has increased and will probably provide important information in the search of orthologous genes as it was done with CALLOSE SYNTHASE5. The development of new probes targeting the cell wall components and the improvement of the technology have also allowed more detailed studies on the cell wall biochemistry and the mechanic of the pollen tube cell wall. Finally, to increase the complexity of the system during their journey pollen tubes travel in the female tissues where additional cell wall interactions, cross-linking, modification, degradation and recycling can occur (Figure 4). The challenge will be to integrate all the parameters from protein signaling and trafficking to cell wall deposition and remodeling in the in vivo context in response to extracellular cues. Solving this complex network of information will unravel the secret of pollen tube tip expansion and guidance.
Very special thanks are due to E.M. Lord (UC Riverside) for having passionately launched JCM onto the fascinating field of pollen tube biology and plant reproduction. JCM is also grateful to all the students who have worked on pollen tubes and our colleagues for the interesting discussions during our lab meetings. The authors wish to thank John Moore (Stellenbosch University, South Africa) and the four anonymous reviewers for their comments and suggestions for improving the quality of the manuscript. This work was partly supported by the University of Rouen and the research network VASI (Plant, Agronomy, Soils and Innovations) of the region Haute-Normandie, France. The authors are grateful to VASI for supporting FD during his PhD and the research network IRIB (Institute for Research and Innovation in Biomedicine) of the region Haute-Normandie, France for the doctoral fellowship to CL.
- Lord, E.M.; Russell, S.D. The mechanisms of pollination and fertilization in plants. Annu. Rev. Cell Dev. Biol. 2002, 18, 81–105. [Google Scholar] [CrossRef]
- Kandasamy, M.K.; Nasrallah, J.B.; Nasrallah, M.E. Pollen-pistil interactions and developmental regulation of pollen tube growth in Arabidopsis. Development 1994, 120, 3405–3418. [Google Scholar]
- Lennon, K.A.; Roy, S.; Hepler, P.K.; Lord, E.M. The structure of the transmitting tissue of Arabidopsis thaliana (L.) and the path of pollen tube growth. Sex. Plant Reprod. 1998, 11, 49–59. [Google Scholar]
- Palanivelu, R.; Preuss, D. Pollen tube targeting and axon guidance: Parallels in tip growth mechanisms. Trends Cell Biol. 2000, 10, 517–524. [Google Scholar] [CrossRef]
- Kim, S.; Mollet, J.C.; Dong, J.; Zhang, K.; Park, S.Y.; Lord, E.M. Chemocyanin, a small basic protein from the lily stigma, induces pollen tube chemotropism. Proc. Natl. Acad. Sci. USA 2003, 100, 16125–16130. [Google Scholar]
- McCormick, S.; Yang, H. Is there more than one way to attract a pollen tube? Trends Plant Sci. 2005, 10, 260–263. [Google Scholar]
- Boavida, L.C.; Vieira, A.M.; Becker, J.D.; Feijò, J.A. Gametophyte interaction and sexual reproduction: How plants make a zygote. Int. J. Dev. Biol. 2005, 49, 615–632. [Google Scholar]
- Johnson, M.A.; Lord, E.M. Extracellular guidance cues and intracellular signaling pathways that direct pollen tube growth. In The Pollen Tube: A Cellular and Molecular Perspective; Malho, R., Ed.; Springer: Berlin, Germany, 2006; Volume 3, pp. 223–242. [Google Scholar]
- Mollet, J.C.; Faugeron, C.; Morvan, H. Cell adhesion, separation and guidance in compatible plant reproduction. Annu. Plant Rev. 2007, 25, 69–90. [Google Scholar]
- Wang, H.J.; Huang, J.C.; Jauh, G.Y. Pollen germination and tube growth. Adv. Bot. Res. 2010, 54, 1–52. [Google Scholar]
- Boisson-Dernier, A.; Kessler, S.A.; Grossniklaus, U. The walls have ears: The role of plant CrRLK1Ls in sensing and transducing extracellular signals. J. Exp. Bot. 2011, 62, 1581–1591. [Google Scholar]
- Geitmann, A.; Steer, M. The Architecture and properties of the pollen tube cell wall. In The Pollen Tube: A Cellular and Molecular Perspective; Malhó, R., Ed.; Springer: Berlin, Germany, 2006; Volume 3, pp. 177–200. [Google Scholar]
- Geitmann, A. How to shape a cylinder: Pollen tube as a model system for the generation of complex cellular geometry. Sex. Plant Reprod. 2010, 23, 63–71. [Google Scholar]
- Nguema-Ona, E.; Coimbra, S.; Vicré-Gibouin, M.; Mollet, J.C.; Driouich, A. Arabinogalactan-proteins in root and pollen tube cells: Distribution and functional aspects. Ann. Bot. 2012, 110, 383–404. [Google Scholar]
- Cheung, A.Y.; Wu, H.M. Structural and signalling networks for the polar cell growth machinery in pollen tubes. Annu. Rev. Plant Biol. 2008, 59, 547–572. [Google Scholar]
- Moscatelli, A.; Ciampolini, F.; Rodigheiro, S.; Onelli, E.; Cresti, M.; Santo, N.; Idilli, A. Distinct endocytosis pathways identified in tobacco pollen tubes using charged nanogold. J. Cell Sci. 2007, 120, 3804–3819. [Google Scholar]
- Bove, J.; Vaillancourt, B.; Kroeger, J.; Hepler, P.K.; Wiseman, P.W.; Geitmann, A. Magnitude and direction of vesicle dynamics in growing pollen tubes using spatiotemporal image correlation spectroscopy and fluorescence recovery after photobleaching. Plant Physiol. 2008, 147, 1646–1658. [Google Scholar]
- Moscatelli, A.; Idilli, A.I. Pollen tube growth: A delicate equilibrium between secretory and endocytic pathways. J. Integr. Plant Biol. 2009, 51, 727–739. [Google Scholar]
- Zonia, L. Spatial and temporal integration of signalling networks regulating pollen tube growth. J. Exp. Bot. 2010, 61, 1939–1957. [Google Scholar]
- Roy, S.; Eckard, K.J.; Lancelle, S.; Hepler, P.K.; Lord, E.M. High-pressure freezing improves the ultrastructural preservation of in vivo grown lily pollen tubes. Protoplasma 1997, 20, 87–98. [Google Scholar]
- Li, Y.Q.; Faleri, C.; Geitmann, A.; Zhang, H.Q.; Cresti, M. Immunogold localization of arabinogalactan proteins, unesterified and esterified pectins in pollen grains and pollen tubes of Nicotiana tabacum L. Protoplasma 1995, 189, 26–36. [Google Scholar]
- Ferguson, C.; Teeri, T.T.; Siika-aho, M.; Read, S.M.; Bacic, A. Location of cellulose and callose in pollen tubes and grains of Nicotiana tabacum. Planta 1998, 206, 452–460. [Google Scholar]
- Lennon, K.A.; Lord, E.M. The in vivo pollen tube cell of Arabidopsis thaliana. I. Tube cell cytoplasm and wall. Protoplasma 2000, 214, 45–56. [Google Scholar]
- Derksen, J.; Knuiman, B.; Hoedemaekers, K.; Guyon, A.; Bonhomme, S.; Pierson, E.S. Growth and cellular organization of Arabidopsis pollen tubes in vitro. Sex. Plant Reprod. 2002, 15, 133–139. [Google Scholar]
- Dardelle, F.; Lehner, A.; Ramdani, Y.; Bardor, M.; Lerouge, P.; Driouich, A.; Mollet, J.C. Biochemical and immunocytological characterizations of Arabidopsis thaliana pollen tube cell wall. Plant Physiol. 2010, 153, 1563–1576. [Google Scholar]
- Chebli, Y.; Kaneda, M.; Zerzour, R.; Geitmann, A. The cell wall of the Arabidopsis thaliana pollen tube—Spatial distribution, recycling and network formation of polysaccharides. Plant Physiol. 2012, 160, 1940–1955. [Google Scholar]
- Derksen, J.; Li, Y.Q.; Knuiman, B.; Geurts, H. The wall of Pinus sylvestris L. pollen tubes. Protoplasma 1999, 208, 26–36. [Google Scholar]
- Yatomi, R.; Nakamura, S.; Nakamura, N. Immunochemical and cytochemical detection of wall components of germinated pollen of Gymnosperms. Grana 2002, 41, 21–28. [Google Scholar]
- Qin, Y.; Chen, D.; Zhao, J. Localization of arabinogalactan proteins in anther, pollen, and pollen tube of Nicotiana tabacum L. Protoplasma 2007, 231, 43–53. [Google Scholar]
- Parre, E.; Geitmann, A. Pectin and the role of the physical properties of the cell wall in pollen tube growth of Solanum chacoense. Planta 2005, 220, 582–592. [Google Scholar]
- Hasegawa, Y.; Nakamura, S.; Kakizoe, S.; Sato, M.; Nakamura, N. Immunocytochemical and chemical analyses of Golgi vesicles isolated from the germinated pollen of Camellia japonica. J. Plant Res. 1998, 111, 421–429. [Google Scholar]
- Wu, J.Z.; Lin, Y.; Zhang, X.L.; Pang, D.W.; Zhao, J. IAA stimulates pollen tube growth and mediates the modification of its wall composition and structure in Torenia fournieri. J. Exp. Bot. 2008, 59, 2529–2543. [Google Scholar]
- Abreu, I.; Oliveira, M. Immunolocalisation of arabinogalactan proteins and pectins in Actinidia deliciosa pollen. Protoplasma 2004, 224, 123–128. [Google Scholar]
- Puhlmann, J.; Bucheli, E.; Swain, M.J.; Dunning, N.; Albersheim, P.; Darvill, A.G.; Hahn, M.G. Generation of monoclonal antibodies against plant cell wall polysaccharides. I. Characterization of a monoclonal antibody to a terminal alpha-(1,2)-linked fucosyl-containing epitope. Plant Physiol. 1994, 104, 699–710. [Google Scholar]
- Marcus, S.E.; Verhertbruggen, Y.; Herve, C.; Ordaz-Ortiz, J.J.; Farkas, V.; Pedersen, H.L.; Willats, W.G.T.; Knox, J.P. Pectic homogalacturonan masks abundant sets of xyloglucan epitopes in plant cell walls. BMC Plant Biol. 2008, 8, 60–71. [Google Scholar]
- Clausen, M.H.; Willats, W.G.T.; Knox, J.P. Synthetic methyl hexagalacturonate hapten inhibitors of anti-homogalacturonan monoclonal antibodies LM7, JIM5 and JIM7. Carbohydr. Res. 2003, 338, 1797–1800. [Google Scholar]
- Verhertbruggen, Y.; Marcus, S.E.; Haeger, A.; Ordaz-Ortiz, J.J.; Knox, J.P. An extended set of monoclonal antibodies to pectic homogalacturonan. Carbohydr. Res. 2009, 344, 1858–1862. [Google Scholar]
- Willats, W.G.T.; McCartney, L.; Steele-King, C.G.; Marcus, S.E.; Mort, A.; Huisman, M.; van Alebeek, G.-J.; Schols, H.A.; Voragen, A.G.J.; Le Goff, A.; et al. A xylogalacturonan epitope is specifically associated with plant cell detachment. Planta 2004, 218, 673–681. [Google Scholar]
- Jones, L.; Seymour, G.B.; Knox, J.P. Localization of pectic galactan in tomato cell walls using a monoclonal antibody specific to (1->4)-beta-d-galactan. Plant Physiol. 1997, 113, 1405–1412. [Google Scholar]
- Willats, W.G.T.; Marcus, S.E.; Knox, J.P. Generation of a monoclonal antibody specific to (1->5)-alpha-l-arabinan. Carbohydr. Res. 1998, 308, 149–152. [Google Scholar]
- Moller, I.; Marcus, S.E.; Haeger, A.; Verhertbruggen, Y.; Verhoef, R.; Schols, H.; Mikklesen, J.D.; Knox, J.P.; Willats, W. High-throughput screening of monoclonal antibodies against plant cell wall glycans by hierarchial clustering of their carbohydrate microarray binding profiles. Glycoconj. J. 2008, 25, 49–58. [Google Scholar]
- Meikle, P.J.; Bonig, I.; Hoogenraad, N.J.; Clarke, A.E.; Stone, B.A. The location of (1→3)-beta-glucans in the walls of pollen tubes of Nicotiana alata using a (1→3)-beta-glucan-specific monoclonal antibody. Planta 1991, 185, 1–8. [Google Scholar]
- Matoh, T.; Takasaki, M.; Takabe, K.; Kobayashi, M. Immunocytochemistry of rhamnogalacturonan II in cell walls of higher Plants. Plant Cell Physiol. 1998, 39, 483–491. [Google Scholar]
- Johnson-Brousseau, S.A.; McCormick, S. A compendium of methods useful for characterizing Arabidopsis pollen mutants and gametophytically expressed genes. Plant J. 2004, 39, 761–775. [Google Scholar]
- Rounds, C.M.; Lubeck, E.; Hepler, P.K.; Winship, L.J. Propidium iodide competes with Ca2+ to label pectin in pollen tubes and Arabidopsis root hairs. Plant Physiol. 2011, 157, 175–187. [Google Scholar]
- Blake, A.W.; McCartney, L.; Flint, J.E.; Bolam, D.N.; Boraston, A.B.; Gilbert, H.J.; Knox, J.P. Understanding the biological rationale for the diversity of cellulose-directed carbohydrate-binding molecules in prokaryotic enzymes. J. Biol. Chem. 2006, 281, 29321–29329. [Google Scholar]
- WallMbDB. Available online: http://glycomics.ccrc.uga.edu/wall2/jsp/abIndex.jsp/ (accessed on 6 November 2012).
- Jauh, G.Y.; Lord, E.M. Localization of pectins and arabinogalactan-proteins in lily (Lilium longiflorum L.) pollen tube and style, and their possible roles in pollination. Planta 1996, 199, 251–261. [Google Scholar]
- Mollet, J.C.; Kim, S.; Jauh, G.Y.; Lord, E.M. AGPs, pollen tube growth and the reversible effects of Yariv phenylglycoside. Protoplasma 2002, 219, 89–98. [Google Scholar]
- Rubinstein, A.L.; Márque, J.; Cervera, M.S.; Bedinger, P.A. Extensin-like glycoproteins in the maize pollen tube wall. Plant Cell 1995, 7, 2211–2225. [Google Scholar]
- Chen, T.; Teng, N.J.; Wu, X.Q.; Wang, Y.H.; Tang, W.; Šamaj, J.; Baluška, F.; Lin, J.X. Disruption of actin filaments by latrunculin B affects cell wall construction in Picea meyeri pollen tube by disturbing vesicle trafficking. Plant Cell Physiol. 2007, 48, 19–30. [Google Scholar]
- Fernando, D.D.; Quinn, C.R.; Brenner, E.; Owens, J.N. Male gametophyte development and evolution in Gymnosperms. Int. J. Plant Dev. Biol. 2010, 4, 47–63. [Google Scholar]
- Parre, E.; Geitmann, A. More than a leak sealant. The mechanical properties of callose in pollen tubes. Plant Physiol. 2005, 137, 274–286. [Google Scholar] [CrossRef]
- Derksen, J.; Janssen, G.J.; Wolters-Arts, M.; Lichtscheidl, I.; Adlassnig, W.; Ovecka, M.; Doris, F.; Steer, M. Wall architecture with high porosity is established at the tip and maintained in growing pollen tubes of Nicotiana tabacum. Plant J. 2011, 68, 495–506. [Google Scholar] [CrossRef]
- Abercrombie, J.M.; O’Meara, B.C.; Moffatt, A.R.; Williams, J.H. Developmental evolution of flowering plant pollen tube cell walls: Callose synthase (CalS) gene expression patterns. EvoDevo 2011, 2, 14. [Google Scholar] [CrossRef]
- Lazzaro, M.D.; Donohue, J.M.; Soodavar, F.M. Disruption of cellulose synthesis by isoxaben causes tip swelling and disorganizes cortical microtubules in elongating conifer pollen tubes. Protoplasma 2003, 220, 201–207. [Google Scholar] [CrossRef]
- Caffall, K.H.; Mohnen, D. The structure, function, and biosynthesis of plant cell wall pectic polysaccharides. Carbohydr. Res. 2009, 344, 1879–1900. [Google Scholar] [CrossRef]
- Micheli, F. Pectin methylesterases: Cell wall enzymes with important roles in plant physiology. Trends Plant Sci. 2001, 6, 414–419. [Google Scholar] [CrossRef]
- Stepka, M.; Ciampolini, F.; Charzynska, M.; Cresti, M. Localization of pectins in the pollen tube wall of Ornithogalum virens L. Does the pattern of pectin distribution depend on the growth rate of the pollen tube? Planta 2000, 210, 630–635. [Google Scholar]
- Li, Y.Q.; Chen, F.; Linskens, H.F.; Cresti, M. Distribution of unesterified and esterified pectins in cell walls of pollen tubes of flowering plants. Sex. Plant Reprod. 1994, 7, 145–152. [Google Scholar]
- Chen, K.M.; Wu, G.L.; Wang, Y.H.; Tian, C.T.; Samaj, J.; Baluska, F.; Lin, J.X. The block of intracellular calcium release affects the pollen tube development of Picea wilsonii by changing the deposition of cell wall components. Protoplasma 2008, 233, 39–49. [Google Scholar] [CrossRef]
- Willats, W.G.T.; Orfila, C.; Limberg, G.; Buchholt, H.C.; van Alebeek, G.-J.; Voragen, A.G.J.; Marcus, S.E.; Christensen, T.M.; Mikkelsen, J.D.; Murray, B.S.; et al. Modulation of the degree and pattern of methyl-esterification of pectic homogalacturonan in plant cell walls: implications for pectin methyl esterase action, matrix properties, and cell adhesion. J. Biol. Chem. 2001, 276, 19404–19413. [Google Scholar]
- Fayant, P.; Girlanda, O.; Chebli, Y.; Aubin, C.; Villemure, I.; Geitmann, A. Finite element model of polar growth in pollen tubes. Plant Cell 2010, 22, 2579–2593. [Google Scholar] [CrossRef]
- APGIII. Angiosperm Phylogeny Group. An update of the Angiosperm phylogeny group classification for the orders and families of flowering plants. Bot. J. Linn. Soc. 2009, 161, 105–121.
- Fry, S.C. Cell wall polysaccharide composition and covalent crosslinking. Annu. Plant Rev. 2011, 41, 1–42. [Google Scholar]
- Scheller, H.V.; Ulvskov, P. Hemicelluloses. Annu. Rev. Plant Biol. 2010, 61, 263–289. [Google Scholar] [CrossRef]
- Cosgrove, D.J. Enzymes and other agents that enhance cell wall extensibility. Annu. Rev. Plant Physiol. Plant Mol. Biol. 1999, 50, 391–417. [Google Scholar] [CrossRef]
- Freshour, G.; Bonin, C.P.; Reiter, W.D.; Albersheim, P.; Darvill, A.G.; Hahn, M.G. Distribution of fucose-containing xyloglucans in cell walls of the mur1 mutant of Arabidopsis. Plant Physiol. 2003, 131, 1602–1612. [Google Scholar] [CrossRef]
- Williams, J.H. Novelties of the flowering plant pollen tube underlie diversification of a key life history stage. Proc. Natl. Acad. Sci. USA 2008, 105, 11259–11263. [Google Scholar] [CrossRef]
- Laughlin, S.T.; Bertozzi, C.R. Imaging the glycome. Proc. Natl. Acad. Sci. USA 2009, 106, 12–17. [Google Scholar] [CrossRef]
- Anderson, C.T.; Wallace, I.S. Illuminating the wall: Using click chemistry to image pectins in Arabidopsis cell walls. Plant Signal. Behav. 2012, 7, 661–663. [Google Scholar] [CrossRef]
- Anderson, C.T.; Wallace, I.S.; Somerville, C.R. Metabolic click-labeling with a fucose analog reveals pectin delivery, architecture, and dynamics in Arabidopsis cell walls. Proc. Natl. Acad. Sci. USA 2012, 109, 1329–1334. [Google Scholar]
- Rae, A.L.; Harris, P.J.; Bacic, A.; Clarke, A.E. Composition of the cell walls of Nicotiana alata Link et Otto pollen tubes. Planta 1985, 166, 128–133. [Google Scholar] [CrossRef]
- Nakamura, N.; Suzuki, H. Sugar composition of pollen grain and pollen tube cell walls. Phytochemistry 1981, 20, 981–984. [Google Scholar]
- Fry, S.C.; York, W.S.; Albersheim, P.; Darvill, A.; Hayashi, T.; Joseleau, J.P.; Seitz, H.U.; Kato, Y.; Pérez Lorences, E.; Maclachlan, G.A.; et al. An unambiguous nomenclature for xyloglucan-derived oligosaccharides. Physiol. Plant 1993, 89, 1–3. [Google Scholar] [CrossRef]
- Cavalier, D.M.; Lerouxel, O.; Neumetzler, L.; Yamauchi, K.; Reinecke, A.; Freshour, G.; Zabotina, O.A.; Hahn, M.G.; Burgert, I.; Pauly, M.; et al. Disrupting two Arabidopsis thaliana xylosyltransferase genes results in plants deficient in xyloglucan, a major primary cell wall component. Plant Cell 2008, 20, 1519–1537. [Google Scholar] [CrossRef]
- Günl, M.; Kraemer, F.; Pauly, M. Oligosaccharide Mass Profiling (OLIMP) of Cell Wall Polysaccharides by MALDI-TOF/MS. In The Plant Cell Wall: Methods and Protocols, Methods in Molecular Biology; Popper, Z.A., Ed.; Springer, Humana Press: New York, NY, USA, 2011; Volume 715, pp. 43–54. [Google Scholar]
- Lerouxel, O.; Choo, T.S.; Seveno, M.; Usadel, B.; Faye, L.; Lerouge, P.; Pauly, M. Rapid structural phenotyping of plant cell wall mutants by enzymatic oligosaccharide fingerprinting. Plant Physiol. 2002, 130, 1754–1763. [Google Scholar] [CrossRef]
- Copyright American Society of Plant Biologists. Available online: http://www.plantphysiol.org/ (accessed on 19 February 2013).
- Sekkal, M.; Huvenne, J.-P.; Legrand, P.; Sombret, B.; Mollet, J.-C.; Mouradi-Givernaud, A.; Verdus, M.-C. Direct structural identification of polysaccharides from red algae by FTIR microspectrometry. I. Localization of agar in Gracilaria verrucosa sections. Microchim. Acta 1993, 112, 1–10. [Google Scholar] [CrossRef]
- Chen, L.; Carpita, N.C.; Reiter, W.D.; Wilson, R.H.; Jeffries, C.; McCann, M.C. A rapid method to screen for cell-wall mutants using discriminant analysis of Fourier transform infrared spectra. Plant J. 1998, 16, 385–392. [Google Scholar] [CrossRef]
- Mouille, G.; Robin, S.; Lecomte, M.; Pagant, S.; Höfte, H. Classification and identification of Arabidopsis cell wall mutants using Fourier-Transform InfraRed (FT-IR) microspectroscopy. Plant J. 2003, 35, 393–404. [Google Scholar] [CrossRef]
- Wang, Q.; Lu, L.; Wu, X.; Li, Y.; Lin, J. Boron influences pollen germination and pollen tube growth in Picea meyeri. Tree Physiol. 2003, 23, 345–351. [Google Scholar] [CrossRef]
- Wang, Q.L.; Kong, L.A.; Hao, H.Q.; Wang, X.H.; Lin, J.X.; Samaj, J.; Baluska, F. Effects of brefeldin A on pollen germination and tube growth: Antagonistic effects on endocytosis and secretion. Plant Physiol. 2005, 139, 1692–1703. [Google Scholar] [CrossRef]
- Wang, Y.; Chen, T.; Zhang, C.; Hao, H.; Liu, P.; Zheng, M.; Baluska, F.; Samaj, J.; Lin, J. Nitric oxide modulates the influx of extracellular Ca2+ and actin filament organization during cell wall construction in Pinus bungeana pollen tubes. New Phytol. 2009, 182, 851–862. [Google Scholar] [CrossRef]
- Mohnen, D. Pectin structure and biosynthesis. Curr. Opin. Plant Biol. 2008, 11, 266–277. [Google Scholar] [CrossRef]
- Driouich, A.; Follet-Gueye, M.L.; Bernard, S.; Kousar, S.; Chevalier, L.; Vicré-Gibouin, M.; Lerouxel, O. Golgi-mediated synthesis and secretion of matrix polysaccharides of the primary cell wall of higher plants. Front. Plant Sci. 2012, 3. [Google Scholar] [CrossRef]
- Akita, K.; Ishimizu, T.; Tsukamoto, T.; Ando, T.; Hase, S. Successive glycosyltransfer activity and enzymatic characterization of pectic polygalacturonate 4-alpha-galacturonosyltransferase solubilized from pollen tubes of Petunia axillaris using pyridylaminated oligogalacturonates as substrates. Plant Physiol. 2002, 130, 374–379. [Google Scholar] [CrossRef]
- Caffall, K.H.; Pattathil, S.; Phillips, S.; Hahn, M.G.; Mohnen, D. Arabidopsis thaliana T-DNA mutants implicate GAUT genes in the biosynthesis of pectin and xylan in cell walls and seed testa. Mol. Plant 2009, 2, 1000–1014. [Google Scholar]
- Kong, Y.; Zhou, G.; Yin, Y.; Xu, Y.; Pattathil, S.; Hahn, M.G. Molecular analysis of a family of Arabidopsis genes related to galacturonosyltransferases. Plant Physiol. 2011, 155, 1791–1805. [Google Scholar] [CrossRef]
- Sterling, J.D.; Atmodjo, M.A.; Inwood, S.E.; Kumar Kolli, V.S.; Quigley, H.F.; Hahn, M.G.; Mohnen, D. Functional identification of an Arabidopsis pectin biosynthetic homogalacturonan galacturonosyltransferase. Proc. Natl. Acad. Sci. USA 2006, 103, 5236–5241. [Google Scholar]
- Bouton, S.; Leboeuf, E.; Mouille, G.; Leydecker, M.T.; Talbotec, J.; Granier, F.; Lahaye, M.; Höfte, H.; Truong, H.N. QUASIMODO1 encodes a putative membrane-bound glycosyltransferase required for normal pectin synthesis and cell adhesion in Arabidopsis. Plant Cell 2002, 14, 2577–2590. [Google Scholar] [CrossRef]
- Qin, Y.; Leydon, A.R.; Manziello, A.; Pandey, R.; Mount, D.; Denic, S.; Vasic, B.; Johnson, M.A.; Palanivelu, R. Penetration of the stigma and style elicits a novel transcriptome in pollen tubes, Pointing to genes critical for growth in a pistil. PLoS Genet. 2009, 5, e1000621. [Google Scholar] [CrossRef]
- Jensen, J.K.; Sørensen, S.O.; Harholt, J.; Geshi, N.; Sakuragi, Y.; Møller, I.; Zandleven, J.; Bernal, A.J.; Jensen, N.B.; Sørensen, C.; et al. Identification of a xylogalacturonan xylosyltransferase involved in pectin biosynthesis in Arabidopsis. Plant Cell 2008, 20, 1289–1302. [Google Scholar] [CrossRef]
- Harholt, J.; Suttangkakul, A.; Scheller, H.V. Biosynthesis of pectin. Plant Physiol. 2010, 153, 384–395. [Google Scholar] [CrossRef]
- Konishi, T.; Takeda, T.; Miyazaki, Y.; Ohnishi-Kameyama, M.; Hayashi, T.; O'Neill, M.A.; Ishii, T. A plant mutase that interconverts UDP-arabinofuranose and UDP-arabinopyranose. Glycobiology 2007, 17, 345–354. [Google Scholar]
- Drakakaki, G.; Zabotina, O.; Delgado, I.; Robert, S.; Keegstra, K.; Raikhel, N. Arabidopsis reversibly glycosylated polypeptides 1 and 2 are essential for pollen development. Plant Physiol. 2006, 142, 1480–1492. [Google Scholar] [CrossRef]
- Rautengarten, C.; Ebert, B.; Herter, T.; Petzold, C.J.; Ishii, T.; Mukhopadhyay, A.; Usadel, B.; Scheller, H.V. The interconversion of UDP-arabinopyranose and UDP-arabinofuranose is indispensable for plant development in Arabidopsis. Plant Cell 2011, 23, 1373–1390. [Google Scholar] [CrossRef]
- Iwai, H.; Hokura, A.; Oishi, M.; Chida, H.; Ishii, T.; Sakai, S.; Satoh, S. The gene responsible for borate cross-linking of pectin Rhamnogalacturonan-II is required for plant reproductive tissue development and fertilization. Proc. Natl. Acad. Sci. USA 2006, 103, 16592–16597. [Google Scholar]
- Wu, A.M.; Rihouey, C.; Seveno, M.; Hörnblad, E.; Singh, S.; Matsunaga, T.; Ishii, T.; Lerouge, P.; Marchant, A. The Arabidopsis IRX10 and IRX10-LIKE glycosyltransferases are critical for glucuronoxylan biosynthesis during secondary cell wall formation. Plant J. 2009, 57, 718–731. [Google Scholar] [CrossRef]
- Brown, D.M.; Zhang, Z.; Stephens, E.; Dupree, P.; Turner, S.R. Characterization of IRX10 and IRX10-like reveals an essential role in glucuronoxylan biosynthesis in Arabidopsis. Plant J. 2009, 57, 732–746. [Google Scholar] [CrossRef]
- Delmas, F.; Séveno, M.; Northey, J.G.; Hernould, M.; Lerouge, P.; McCourt, P.; Chevalier, C. The synthesis of the rhamnogalacturonan II component 3-deoxy-d-manno-2-octulosonic acid (Kdo) is required for pollen tube growth and elongation. J. Exp. Bot. 2008, 59, 2639–2647. [Google Scholar] [CrossRef]
- Liu, X.L.; Liu, L.; Niu, Q.K.; Xia, C.; Yang, K.Z.; Li, R.; Chen, L.Q.; Zhang, X.Q.; Zhou, Y.; Ye, D. Male gametophyte defective 4 encodes a rhamnogalacturonan II xylosyltransferase and is important for growth of pollen tubes and roots in Arabidopsis. Plant J. 2011, 65, 647–660. [Google Scholar] [CrossRef]
- Deng, Y.; Wang, W.; Li, W.Q.; Xia, C.; Liao, H.Z.; Zhang, X.Q.; Ye, D. MALE GAMETOPHYTE DEFECTIVE 2, encoding a sialyltransferase-like protein, is required for normal pollen germination and pollen tube growth in Arabidopsis. J. Integr. Plant Biol. 2010, 52, 829–843. [Google Scholar] [CrossRef]
- Kobayashi, M.; Kouzu, N.; Inami, A.; Toyooka, K.; Konishi, Y.; Matsuoka, K.; Matoh, T. Characterization of Arabidopsis CTP:3-deoxy-d-manno-2-octulosonate cytidylyltransferase (CMP-KDO synthetase), the enzyme that activates KDO during rhamnogalacturonan II biosynthesis. Plant Cell Physiol. 2011, 52, 1832–1843. [Google Scholar] [CrossRef]
- Goubet, F.; Mohnen, D. Solubilization and partial characterization of homogalacturonan-methyltransferase from microsomal membranes of suspension-cultured tobacco cells. Plant Physiol. 1999, 121, 281–290. [Google Scholar] [CrossRef]
- Pauly, M.; Scheller, H.V. O-Acetylation of plant cell wall polysaccharides: Identification and partial characterization of a rhamnogalacturonan O-acetyl-transferase from potato suspension-cultured cells. Planta 2000, 210, 659–667. [Google Scholar] [CrossRef]
- Mouille, G.; Ralet, M.C.; Cavelier, C.; Eland, C.; Effroy, D.; Hématy, K.; McCartney, L.; Truong, H.N.; Gaudon, V.; Thibault, J.F.; et al. Homogalacturonan synthesis in Arabidopsis thaliana requires a Golgi-localized protein with a putative methyltransferase domain. Plant J. 2007, 50, 605–614. [Google Scholar]
- Miao, Y.; Li, H.Y.; Shen, J.; Wang, J.; Jiang, L. QUASIMODO 3 (QUA3) is a putative homogalacturonan methyltransferase regulating cell wall biosynthesis in Arabidopsis suspension-cultured cells. J. Exp. Bot. 2011, 62, 5063–5078. [Google Scholar] [CrossRef]
- Manabe, Y.; Nafisi, M.; Verhertbruggen, Y.; Orfila, C.; Gille, S.; Rautengarten, C.; Cherk, C.; Marcus, S.E.; Somerville, S.; Pauly, M.; et al. Loss-of-function mutation of REDUCED WALL ACETYLATION2 in Arabidopsis leads to reduced cell wall acetylation and increased resistance to Botrytis cinerea. Plant Physiol. 2011, 155, 1068–1078. [Google Scholar] [CrossRef]
- Zabotina, O.A. Xyloglucan and its biosynthesis. Front. Plant Sci. 2012, 3. [Google Scholar] [CrossRef]
- Cocuron, J.C.; Lerouxel, O.; Drakakaki, G.; Alonso, A.P.; Liepman, A.H.; Keegstra, K.; Raikhel, N.; Wilkerson, C.G. A gene from the cellulose synthase-like C family encodes a beta-1,4 glucan synthase. Proc. Natl. Acad. Sci. USA 2007, 104, 8550–8555. [Google Scholar] [CrossRef]
- Cavalier, D.M.; Keegstra, K. Two xyloglucan xylosyltransferases catalyze the addition of multiple xylosyl residues to cellohexaose. J. Biol. Chem. 2006, 281, 34197–34207. [Google Scholar] [CrossRef]
- Vuttipongchaikij, S.; Brocklehurst, D.; Steele-King, C.; Ashford, D.A.; Gomez, L.D.; McQueen-Mason, S.J. Arabidopsis GT34 family contains five xyloglucan α-1,6-xylosyltransferases. New Phytol. 2012, 195, 585–595. [Google Scholar] [CrossRef]
- Madson, M.; Dunand, C.; Li, X.; Verma, R.; Vanzin, G.F.; Caplan, J.; Shoue, D.A.; Carpita, N.C.; Reiter, W.D. The MUR3 gene of Arabidopsis encodes a xyloglucan galactosyltransferase that is evolutionarily related to animal exostosins. Plant Cell 2003, 15, 1662–1670. [Google Scholar] [CrossRef]
- Jensen, J.K.; Schultink, A.; Keegstra, K.; Wilkerson, C.G.; Pauly, M. RNA-Seq analysis of developing nasturtium seeds (Tropaeolum majus): Identification and characterization of an additional galactosyltransferase involved in xyloglucan biosynthesis. Mol. Plant 2012, 5, 984–992. [Google Scholar]
- Perrin, R.M.; DeRocher, A.E.; Bar-Peled, M.; Zeng, W.; Norambuena, L.; Orellana, A.; Raikhel, N.V.; Keegstra, K. Xyloglucan fucosyltransferase, an enzyme involved in plant cell wall biosynthesis. Science 1999, 284, 1976–1979. [Google Scholar] [CrossRef]
- Vanzin, G.F.; Madson, M.; Carpita, N.C.; Raikhel, N.V.; Keegstra, K.; Reiter, W.D. The mur2 mutant of Arabidopsis thaliana lacks fucosylated xyloglucan because of a lesion in fucosyltransferase AtFUT1. Proc. Natl. Acad. Sci. USA 2002, 99, 3340–3345. [Google Scholar]
- Guerriero, G.; Fugelstad, J.; Bulone, V. What do we really know about cellulose biosynthesis in Higher Plants? J. Integr. Plant Biol. 2010, 52, 161–175. [Google Scholar] [CrossRef]
- Richmond, T. Higher plant cellulose synthases. Genome Biol. 2000, 1, reviews3001.1–reviews3001.6. [Google Scholar] [CrossRef]
- Doblin, M.S.; Kurek, I.; Jacob-Wilk, D.; Delmer, D.P. Cellulose biosynthesis in plants: From genes to rosettes. Plant Cell Physiol. 2002, 43, 1407–1420. [Google Scholar] [CrossRef]
- Richmond, T.A.; Somerville, C.R. Integrative approaches to determining Csl function. Plant Mol. Biol. 2001, 47, 131–143. [Google Scholar] [CrossRef]
- Bernal, A.J.; Yoo, C.M.; Mutwil, M.; Jensen, J.K.; Hou, G.; Blaukopf, C.; Sørensen, I.; Blancaflor, E.B.; Scheller, H.V.; Willats, W.G. Functional analysis of the cellulose synthase-like genes CSLD1, CSLD2, and CSLD4 in tip-growing Arabidopsis cells. Plant Physiol. 2008, 148, 1238–1253. [Google Scholar] [CrossRef]
- Wang, L.; Guo, K.; Li, Y.; Tu, Y.; Hu, H.; Wang, B.; Cui, X.; Peng, L. Expression profiling and integrative analysis of the CESA/CSL superfamily in rice. BMC Plant Biol. 2010, 10, 282. [Google Scholar] [CrossRef]
- Doblin, M.S.; de Melis, L.; Newbigin, E.; Bacic, A.; Read, S.M. Pollen tubes of Nicotiana alata express two genes from different β-Glucan synthase families. Plant Physiol. 2001, 125, 2040–2052. [Google Scholar]
- Cai, G.; Faleri, C.; Del Casino, C.; Emons, A.M.C.; Cresti, M. Distribution of callose synthase, cellulose synthase, and sucrose synthase in tobacco pollen tube is controlled in dissimilar ways by actin filaments and microtubules. Plant Physiol. 2011, 155, 1169–1190. [Google Scholar] [CrossRef]
- Wang, W.; Wang, L.; Chen, C.; Xiong, G.; Tan, X.Y.; Yang, K.Z.; Wang, Z.C.; Zhou, Y.; Ye, D.; Chen, L.Q. Arabidopsis CSLD1 and CSLD4 are required for cellulose deposition and normal growth of pollen tubes. J. Exp. Bot. 2011, 62, 5161–5177. [Google Scholar] [CrossRef]
- Persson, S.; Paredez, A.; Carroll, A.; Palsdottir, H.; Doblin, M.; Poindexter, P.; Khitrov, N.; Auer, M.; Somerville, C.R. Genetic evidence for three unique components in primary cell-wall cellulose synthase complexes in Arabidopsis. Proc. Natl. Acad. Sci. USA 2007, 104, 15566–15571. [Google Scholar] [CrossRef]
- Boavida, L.C.; Shuai, B.; Yu, H.J.; Pagnussat, G.C.; Sundaresan, V.; McCormick, S. A collection of Ds insertional mutants associated with defects in male gametophyte development and function in Arabidopsis thaliana. Genetics 2009, 181, 1369–1385. [Google Scholar]
- Verma, D.P.; Hong, Z. Plant callose synthase complexes. Plant Mol. Biol. 2001, 47, 693–701. [Google Scholar] [CrossRef]
- Nishikawa, S.; Zinkl, G.M.; Swanson, R.J.; Maruyama, D.; Preuss, D. Callose (beta-1,3 glucan) is essential for Arabidopsis pollen wall patterning, but not tube growth. BMC Plant Biol. 2005, 5, 15. [Google Scholar] [CrossRef]
- Dong, X.; Hong, Z.; Sivaramakrishnan, M.; Mahfouz, M.; Verma, D.P. Callose synthase (CalS5) is required for exine formation during microgametogenesis and for pollen viability in Arabidopsis. Plant J. 2005, 42, 315–328. [Google Scholar] [CrossRef]
- Brownfield, L.; Ford, K.; Doblin, M.S.; Newbigin, E.; Read, S.; Bacic, A. Proteomic and biochemical evidence links the callose synthase in Nicotiana alata pollen tubes to the product of the NaGSL1 gene. Plant J. 2007, 52, 147–156. [Google Scholar] [CrossRef]
- Brownfield, L.; Wilson, S.; Newbigin, E.; Bacic, A.; Read, S. Molecular control of the glucan synthase-like protein NaGSL1 and callose synthesis during growth of Nicotiana alata pollen tubes. Biochem. J. 2008, 414, 43–52. [Google Scholar] [CrossRef]
- Pacini, E.; Franchi, G.G.; Ripaccioli, M. Ripe pollen structure and histochemistry of some Gymnosperms. Plant Syst. Evol. 1999, 217, 81–99. [Google Scholar] [CrossRef]
- McQueen-Mason, S.; Durachko, D.M.; Cosgrove, D.J. Two endogenous proteins that induce cell wall extension in plants. Plant Cell 1992, 4, 1425–1433. [Google Scholar]
- Li, Z.-C.; Durachko, D.M.; Cosgrove, D.J. An oat coleoptile wall protein that induces wall extension in vitro and that is antigenically related to a similar protein from cucumber hypocotyls. Planta 1993, 191, 349–356. [Google Scholar]
- Sampedro, J.; Cosgrove, D.J. The expansin superfamily. Genome Biol. 2005, 6, 1–11. [Google Scholar]
- McQueen-Mason, S.; Cosgrove, D.J. Disruption of hydrogen bonding between plant cell wall polymers by proteins that induce wall extension. Proc. Natl. Acad. Sci. USA 1994, 91, 6574–6578. [Google Scholar] [CrossRef]
- McQueen-Mason, S.; Cosgrove, D.J. Expansin mode of action on cell walls. Analysis of wall hydrolysis, stress relaxation, and binding. Plant Physiol. 1995, 107, 87–100. [Google Scholar]
- Sharova, E.I. Expansins: Proteins involved in cell wall softening during plant growth and morphogenesis. Russ. J. Plant Physiol. 2007, 54, 713–727. [Google Scholar]
- Arabidopsis genes. Available online: https://homes.bio.psu.edu/expansins/arabidopsis.htm/ (accessed on 6 November 2012).
- Dai, S.; Li, L.; Chen, T.; Chong, K.; Xue, Y.; Wang, T. Proteomic analyses of Oryza sativa mature pollen reveal novel proteins associated with pollen germination and tube growth. Proteomics 2006, 6, 2504–2529. [Google Scholar]
- Li, L.C.; Bedinger, P.A.; Volk, C.; Jones, A.D.; Cosgrove, D.J. Purification and characterization of four β-expansins (Zea m 1 Isoforms) from maize pollen. Plant Physiol. 2003, 132, 2073–2085. [Google Scholar]
- Jin, Y.; Tashpulatov, A.S.; Katholnigg, H.; Heberle-Bors, E.; Touraev, A. Isolation and characterization of two wheat β-expansin genes expressed during male gametophyte development. Protoplasma 2006, 228, 13–19. [Google Scholar]
- Zaidi, M.A.; O’Leary, S.; Wu, S.; Gleddie, S.C.; Eudes, F.; Laroche, A.; Robert, L.S. A molecular and proteomic investigation of proteins rapidly released from triticale pollen upon hydration. Plant Mol Biol. 2012, 79, 101–121. [Google Scholar]
- Cosgrove, D.J.; Bedinger, P.; Durachko, D.M. Group 1 allergens of grass pollen as cell wall-loosening agents. Proc. Natl. Acad. Sci.USA 1997, 94, 6559–6564. [Google Scholar]
- Winter, D.; Vinegar, B.; Nahal, H.; Ammar, R.; Wilson, G.V.; Provart, N.J. An “Electronic fluorescent pictograph” browser for exploring and analyzing large-scale biological data sets. PLoS One 2007, 2, e718. [Google Scholar]
- Magrane, M.; UniProt Consortium. UniProt Knowledgebase: A hub of integrated protein data. Database 2011. [Google Scholar] [CrossRef]
- Hende, H.; Bradford, K.J.; Brummel, D.A.; Cho, H.T.; Cosgrove, D.J.; Fleming, A.J.; Gehring, C.; Lee, Y.; McQuenn-Mason, S.; Rose, J.K.C.; et al. Nomenclature for members of the expansin superfamily of genes and proteins. Plant Mol. Biol. 2004, 55, 311–314. [Google Scholar]
- Swanson, R.; Clark, T.; Preuss, D. Expression profiling of Arabidopsis stigma tissue identifies stigma-specific genes. Sex. Plant Reprod. 2005, 18, 163–171. [Google Scholar]
- Rose, J.K.C.; Braam, J.; Fry, S.C.; Nishitani, K. The XTH family of enzymes involved in xyloglucan endotransglucosylation and endohydrolysis: Current perspectives and a new unifying nomenclature. Plant Cell Physiol. 2002, 43, 1421–1435. [Google Scholar]
- Fry, S.C.; Smith, R.C.; Renwick, K.F.; Martin, D.J.; Hodge, S.K.; Matthews, K.J. Xyloglucan endotransglycosylase, a new wall-loosening enzyme activity from plants. Biochem. J. 1992, 282, 821–828. [Google Scholar]
- Nishitani, K.; Tominaga, R. Endo-xyloglucan transferase, a novel class of glycosyltransferase that catalyzes transfer of a segment of xyloglucan molecule to another xyloglucan molecule. J. Biol. Chem. 1992, 267, 21058–21064. [Google Scholar]
- Yokoyama, R.; Nishitani, K. A comprehensive expression analysis of all members of a gene family encoding cell-wall enzymes allowed us to predict cis-regulatory regions involved in cell wall construction in specific organs of Arabidopsis. Plant Cell Physiol. 2001, 42, 1025–1033. [Google Scholar]
- Yokoyama, R.; Rose, J.K.C.; Nishitani, K. A surprising diversity and abundance of xyloglucan endotransglucosylase/hydrolases in rice. Classification and expression analysis. Plant Physiol. 2004, 134, 1088–1099. [Google Scholar]
- Becnel, J.; Natarajan, M.; Kipp, A.; Braam, J. Developmental expression patterns of Arabidopsis XTH genes reported by transgenes and Genevestigator. Plant Mol. Biol. 2006, 61, 451–467. [Google Scholar]
- Kurasawa, K.; Matsui, A.; Yokoyama, R.; Kuriyama, T.; Yoshizumi, T.; Matsui, M.; Suwabe, K.; Watanabe, M.; Nishitani, K. The AtXTH28 gene, a xyloglucan endotransglucosylase/hydrolase, is involved in automatic self-pollination in Arabidopsis thaliana. Plant Cell Physiol. 2009, 50, 413–422. [Google Scholar]
- Zhang, G.F.; Staehelin, L.A. Functional compartmentation of the Golgi apparatus of plant cells: Immunocytochemical analysis of high-pressure frozen- and freeze-substituted sycamore maple suspension culture cells. Plant Physiol. 1992, 99, 1070–1083. [Google Scholar]
- Gaffe, J.; Tieman, D.M.; Handa, A.K. Pectin methylesterase isoforms in tomato (Lycopersicon esculentum) tissues (effects of expression of a pectin methylesterase antisense gene). Plant Physiol. 1994, 105, 199–203. [Google Scholar]
- Rhee, S.Y.; Somerville, C.R. Tetrad pollen formation in quartet mutants of Arabidopsis thaliana is associated with persistence of pectic polysaccharides of the pollen mother cell wall. Plant J. 1998, 15, 79–88. [Google Scholar]
- Rhee, S.Y.; Osborne, E.; Poindexter, P.D.; Somerville, C.R. Microspore separation in the quartet 3 mutants of Arabidopsis is impaired by a defect in a developmentally regulated polygalacturonase required for pollen mother cell-wall degradation. Plant Physiol. 2003, 133, 1170–1180. [Google Scholar]
- Francis, K.E.; Lam, S.Y.; Copenhaver, G.P. Separation of Arabidopsis pollen tetrads is regulated by QUARTET1, a pectin methyl-esterase gene. Plant Physiol. 2006, 142, 1004–1013. [Google Scholar]
- Wolf, S.; Mouille, G.; Pelloux, J. Homogalacturonan methyl-esterification and plant development. Mol. Plant 2009, 2, 851–860. [Google Scholar]
- Zhu, Y.; Zhao, P.; Wu, X.; Wang, W.; Scali, M.; Cresti, M. Proteomic identification of differentially expressed proteins in mature and germinated maize pollen. Acta Physiol. Plant 2011, 33, 1467–1474. [Google Scholar]
- Ge, W.; Song, Y.; Zhang, C.; Zhang, Y.; Burlingame, A.L.; Guo, Y. Proteomic analyses of apoplastic proteins from germinating Arabidopsis thaliana pollen. Biochim. Biophys. Acta 2011, 1814, 1964–1973. [Google Scholar]
- Li, Y.Q.; Mareck, A.; Faleri, C.; Moscatelli, A.; Liu, Q.; Cresti, M. Detection and localization of pectin methylesterase isoforms in pollen tubes of Nicotiana tabacum L. Planta 2002, 214, 734–740. [Google Scholar]
- Jiang, L.; Yang, S.L.; Xie, L.F.; Puah, C.S.; Zhang, X.Q.; Yang, W.C.; Sundaresan, V.; Ye, D. VANGUARD1 encodes a pectin methylesterase that enhances pollen tube growth in the Arabidopsis style and transmitting tract. Plant Cell 2005, 17, 584–596. [Google Scholar]
- Tian, G.W.; Chen, M.H.; Zaltsman, A.; Citovsky, V. Pollen-specific pectin methylesterase involved in pollen tube growth. Dev. Biol. 2006, 294, 83–91. [Google Scholar]
- Bosch, M.; Cheung, A.Y.; Hepler, P.K. Pectin methylesterase, a regulator of pollen tube growth. Plant Physiol. 2005, 138, 1334–1346. [Google Scholar]
- Wolf, S.; Grsic-Rausch, S.; Rausch, T.; Greiner, S. Identification of pollen-expressed pectin methylesterase inhibitors in Arabidopsis. FEBS Lett. 2003, 555, 551–555. [Google Scholar]
- Raiola, A.; Camardella, L.; Giovane, A.; Mattei, B.; de Lorenzo, G.; Cervone, F.; Bellincampi, D. Two Arabidopsis thaliana genes encode functional pectin methylesterase inhibitors. FEBS Lett. 2004, 557, 199–203. [Google Scholar]
- Pina, C.; Pinto, F.; Feijó, J.A.; Becker, J.D. Gene family analysis of the Arabidopsis pollen transcriptome reveals biological implications for cell growth, division control, and gene expression regulation. Plant Physiol. 2005, 138, 744–756. [Google Scholar]
- Zhang, G.Y.; Feng, J.; Wu, J.; Wang, X.W. BoPMEI1, a pollen-specific pectin methylesterase inhibitor, has an essential role in pollen tube growth. Planta 2010, 231, 1323–1334. [Google Scholar]
- Lehner, A.; Leroux, C.; Mollet, J.C. Unpublished work. University of Rouen: Mont Saint-Aignan, France, 2013. [Google Scholar]
- Röckel, N.; Wolf, S.; Kost, B.; Rausch, T.; Greiner, S. Elaborate spatial patterning of cell-wall PME and PMEI at the pollen tube tip involves PMEI endocytosis, and reflects the distribution of esterified and de-esterified pectins. Plant J. 2008, 53, 133–143. [Google Scholar]
- Leboeuf, E.; Guillon, F.; Thoiron, S.; Lahaye, M. Biochemical and immunohistochemical analysis of pectic polysaccharides in the cell walls of Arabidopsis mutant QUASIMODO 1 suspension-cultured cells: Implications for cell adhesion. J. Exp. Bot. 2005, 56, 3171–3182. [Google Scholar]
- Durand, C.; Vicre-Gibouin, M.; Follet-Gueye, M.L.; Duponchel, L.; Moreau, M.; Lerouge, P.; Driouich, A. The organization pattern of root border-likes cells of Arabidopsis thaliana is dependent on cell wall homogalacturonan. Plant Physiol. 2009, 150, 1411–1421. [Google Scholar]
- Mollet, J.C.; Park, S.Y.; Nothnagel, E.A.; Lord, E.M. A lily stylar pectin is necessary for pollen tube adhesion to an in vitro stylar matrix. Plant Cell 2000, 12, 1737–1749. [Google Scholar]
- Park, S.Y.; Jauh, G.Y.; Mollet, J.C.; Eckard, K.J.; Nothnagel, E.A.; Walling, L.L.; Lord, E.M. A lipid transfer-like protein is necessary for lily pollen tube adhesion to an in vitro stylar matrix. Plant Cell 2000, 12, 151–164. [Google Scholar]
- Tung, C.W.; Dwyer, K.G.; Nasrallah, M.E.; Nasrallah, J.B. Genome-wide identification of genes expressed in Arabidopsis pistils specifically along the path of pollen tube growth. Plant Physiol. 2005, 138, 977–989. [Google Scholar]
- Nieuwland, J.; Feron, R.; Huisman, B.A.H.; Fasolino, A.; Hilbers, C.W.; Derksen, J.; Mariani, C. Lipid transfer proteins enhance cell wall extension in tobacco. Plant Cell 2005, 17, 2009–2019. [Google Scholar]
- Chae, K.; Kieslich, C.A.; Morikis, D.; Kim, S.C.; Lord, E.M. A gain-of-function mutation of Arabidopsis lipid transfer protein 5 disturbs pollen tube tip growth and fertilization. Plant Cell 2009, 21, 3902–3914. [Google Scholar]
- Gou, J.Y.; Miller, L.M.; Hou, G.; Yu, X.H.; Chen, X.Y.; Liu, C.J. Acetylesterase-mediated deacetylation of pectin impairs cell elongation, pollen germination and Plant reproduction. Plant Cell 2012, 24, 50–65. [Google Scholar]
- Wing, R.A.; Yamaguchi, J.; Larabell, S.K.; Ursin, V.M.; McCormick, S. Molecular and genetic characterization of two pollen-expressed genes that have sequence similarity to pectate lyases of the plant pathogen Erwinia. Plant Mol. Biol. 1989, 14, 17–28. [Google Scholar]
- Wu, Y.; Qiu, X.; Du, S.; Erickson, L. PO149, a new member of pollen pectate lyase-like gene family from alfalfa. Plant Mol. Biol. 1996, 32, 1037–1042. [Google Scholar]
- Kulikauskas, R.; McCormick, S. Identification of the tobacco and Arabidopsis homologues of the pollen-expressed LAT59 gene of tomato. Plant Mol. Biol. 1997, 34, 809–814. [Google Scholar]
- Marin-Rodriguez, M.V.; Orchard, J.; Seymour, G.B. Pectate lyases, cell wall degradation and fruit softening. J. Exp. Bot. 2002, 53, 2115–2119. [Google Scholar] [CrossRef]
- Palusa, S.G.; Golovkin, M.; Shin, S.B.; Richardson, D.N.; Reddy, A.S. Organ-specific, developmental, hormonal and stress regulation of expression of putative pectate lyase genes in Arabidopsis. New Phytol. 2007, 174, 537–550. [Google Scholar] [CrossRef]
- Sun, L.; van Nocker, S. Analysis of promoter activity of members of the PECTATE LYASE-LIKE (PLL) gene family in cell separation in Arabidopsis. BMC Plant Biol. 2010, 10, 152. [Google Scholar] [CrossRef]
- Dai, S.; Chen, T.; Chong, K.; Xue, Y.; Liu, S.; Wang, T. Proteomics identification of differentially expressed proteins associated with pollen germination and tube growth reveals characteristics of germinated Oryza sativa pollen. Mol. Cell. Proteomics 2007, 6, 207–230. [Google Scholar]
- Henrissat, B. A classification of glycosyl hydrolases based on amino acid sequence similarities. Biochem J. 1991, 280, 309–316. [Google Scholar]
- Glycoside Hydrolase Family Classification. Available online: http://www.cazy.org/Glycoside-Hydrolases.html/ (accessed on 23 October 2012).
- Del Campillo, E.; Lewis, L.N. Occurrence of 9.5 cellulase and other hydrolases in flower reproductive organs undergoing major cell wall disruption. Plant Physiol. 1992, 99, 1015–1020. [Google Scholar] [CrossRef]
- Aouar, L.; Chebli, Y.; Geitmann, A. Morphogenesis of complex plant cell shapes: The mechanical role of crystalline cellulose in growing pollen tubes. Sex. Plant Reprod. 2010, 23, 15–27. [Google Scholar] [CrossRef]
- Roggen, H.P.J.; Stanley, R.G. Cell-wall-hydrolysing enzymes in wall formation as measured by pollen-tube extension. Planta 1969, 84, 295–303. [Google Scholar] [CrossRef]
- Takeda, H.; Yoshikawa, T.; Liu, X.Z.; Nakagawa, N.; Li, Y.Q.; Sakurai, N. Molecular cloning of two exo-beta-glucanases and their in vivo substrates in the cell walls of lily pollen tubes. Plant Cell Physiol. 2004, 45, 436–444. [Google Scholar] [CrossRef]
- Kotake, T.; Li, Y.Q.; Takahashi, M.; Sakurai, N. Characterization and function of wall-bound exo-beta-glucanases of Lilium longiflorum pollen tubes. Sex. Plant Reprod. 2000, 13, 1–9. [Google Scholar] [CrossRef]
- Hruba, P.; Honys, D.; Twell, D.; Capkova, V.; Tupy, J. Expression of beta-galactosidase and beta-xylosidase genes during microspore and pollen development. Planta 2005, 220, 931–940. [Google Scholar] [CrossRef]
- Pressey, R.; Reger, B.J. Polygalacturonase in pollen from corn and other grasses. Plant Sci. 1969, 59, 57–62. [Google Scholar] [CrossRef]
- Hadfield, K.A.; Bennett, A.B. Polygalacturonases: Many genes in search of a function. Plant Physiol. 1998, 117, 337–343. [Google Scholar] [CrossRef]
- Arabidopsis Genome Initiative. Analysis of the genome sequence of the flowering plant Arabidopsis thaliana. Nature 2000, 408, 796–815.
- González-Carranza, Z.H.; Elliott, K.A.; Roberts, J.A. Expression of polygalacturonases and evidence to support their role during cell separation processes in Arabidopsis thaliana. J. Exp. Bot. 2007, 58, 3719–3730. [Google Scholar] [CrossRef]
- Kim, J.; Shiu, S.H.; Thoma, S.; Li, W.H.; Patterson, S.E. Patterns of expansion and expression divergence in the plant polygalacturonase gene family. Genome Biol. 2007, 7, R87. [Google Scholar]
- Torki, M.; Mandaron, P.; Mache, R.; Falconet, D. Characterization of a ubiquitous expressed gene family encoding polygalacturonase in Arabidopsis thaliana. Gene 2000, 242, 427–436. [Google Scholar] [CrossRef]
- Huang, L.; Ye, Y.; Zhang, Y.; Zhang, A.; Liu, T.; Cao, J. BcMF9, a novel polygalacturonase gene, is required for both Brassica campestris intine and exine formation. Ann. Bot. 2009, 104, 1339–1351. [Google Scholar] [CrossRef]
- Huang, L.; Cao, J.; Zhang, A.; Ye, Y.; Zhang, Y.; Liu, T. The polygalacturonase gene BcMF2 from Brassica campestris is associated with intine development. J. Exp. Bot. 2009, 60, 301–313. [Google Scholar]
- Tamari, F.; Shore, J.S. Allelic variation for a short-specific polygalacturonase in Turnera subulata: Is it associated with the degree of self-compatibility? Int. J. Plant Sci. 2006, 167, 125–133. [Google Scholar] [CrossRef]
- Dearnaley, J.D.W.; Daggard, G.A. Expression of a polygalacturonase enzyme in germinating pollen of Brassica napus. Sex. Plant Reprod. 2001, 13, 265–271. [Google Scholar] [CrossRef]
- Bosch, M.; Hepler, P.K. Pectin methylesterases and pectin dynamics in pollen tubes. Plant Cell 2005, 17, 3219–3226. [Google Scholar] [CrossRef]
- Dey, P.M.; del Campillo, E. Biochemistry of the multiple forms of glycosidases in plants. Adv. Enzymol. Relat. Areas Mol. Biol. 1984, 56, 141–249. [Google Scholar]
- Ahn, Y.O.; Zheng, M.; Bevan, D.R.; Esen, A.; Shiu, S.H.; Benson, J.; Peng, H.P.; Miller, J.T.; Cheng, C.L.; Poulton, J.E.; et al. Functional genomic analysis of Arabidopsis thaliana glycoside hydrolase family 35. Phytochemistry 2007, 68, 1510–1520. [Google Scholar] [CrossRef]
- Tanthanuch, W.; Chantarangsee, M.; Maneesan, J.; Ketudat-Cairns, J. Genomic and expression analysis of glycosyl hydrolase family 35 genes from rice (Oryza sativa L.). BMC Plant Biol. 2008, 8, 84. [Google Scholar] [CrossRef]
- Singh, M.B.; Knox, R.B. Grass pollen allergens: Antigenic relationships detected using monoclonal antibodies and dot blotting immunoassay. Int. Arch. Allergy Appl. Immunol. 1985, 78, 300–304. [Google Scholar] [CrossRef]
- Cheung, A.Y.; Wang, H.; Wu, H.M. A floral transmitting tissue-specific glycoprotein attracts pollen tubes and stimulates their growth. Cell 1995, 82, 383–393. [Google Scholar] [CrossRef]
- Wu, H.M.; Wang, H.; Cheung, A.Y. A pollen tube growth stimulatory glycoprotein is deglycosylated by pollen tubes and displays a glycosylation gradient in the flower. Cell 1995, 82, 395–403. [Google Scholar] [CrossRef]
- Rogers, H.J.; Maund, S.L.; Johnson, L.H. A β-galactosidase-like gene is expressed during tobacco pollen development. J. Exp. Bot. 2001, 52, 67–75. [Google Scholar] [CrossRef]
- Walker, M.; Tehseen, M.; Doblin, M.S.; Pettolino, F.A.; Wilson, S.M.; Bacic, A.; Golz, J.F. The transcriptional regulator LEUNIG_HOMOLOG regulates mucilage release from the Arabidopsis testa. Plant Physiol. 2011, 156, 46–60. [Google Scholar] [CrossRef]
- Western, T.L.; Burn, J.; Tan, W.L.; Skinner, D.J.; Martin-McCaffrey, L.; Moffatt, B.A.; Haughn, G.W. Isolation and characterization of mutants defective in seed coat mucilage secretory cell development in Arabidopsis. Plant Physiol. 2001, 127, 998–1011. [Google Scholar] [CrossRef]
- Sampedro, J.; Pardo, B.; Gianzo, C.; Guitian, E.; Revilla, G.; Zarra, I. Lack of alpha-xylosidase activity in Arabidopsis alters xyloglucan composition and results in growth defects. Plant Physiol. 2010, 154, 1105–1115. [Google Scholar] [CrossRef]
- Lehner, A.; Dardelle, F.; Soret-Morvan, O.; Lerouge, P.; Driouich, A.; Mollet, J.C. Pectins in the cell wall of Arabidopsis thaliana pollen tube and pistil. Plant Signal. Behav. 2010, 5, 1282–1285. [Google Scholar] [CrossRef]
- Anderson, J.R.; Barnes, W.S.; Bedinger, P. 2,6-Dichlorobenzonitrile, a cellulose biosynthesis inhibitor, affects morphology and structural integrity of petunia and lily pollen tubes. Plant Physiol. 2002, 159, 61–67. [Google Scholar] [CrossRef]
- Whitney, S.E.C.; Wilson, E.; Webster, J.; Bacic, A.; Reid, J.S.G.; Gidley, M.J. Effects of structural variation in xyloglucan polymers on interactions with bacterial cellulose. Am. J. Bot. 2006, 93, 1402–1414. [Google Scholar] [CrossRef]
- Pena, M.J.; Ryden, P.; Madson, M.; Smith, A.C.; Carpita, N.C. The galactose residues of xyloglucan are essential to maintain mechanical strength of the primary cell walls in Arabidopsis during growth. Plant Physiol. 2004, 134, 443–451. [Google Scholar] [CrossRef]
- Nguema-Ona, E.; Andeme-Onzighi, C.; Aboughe-Angone, S.; Bardor, M.; Ishii, T.; Lerouge, P.; Driouich, A. The reb1-1 mutation of Arabidopsis: Effect on the structure and localization of galactose-containing cell wall polysaccharides. Plant Physiol. 2006, 140, 1406–1417. [Google Scholar] [CrossRef]
- Zabotina, O.A.; van de Ven, W.T.; Freshour, G.; Drakakaki, G.; Cavalier, D.; Mouille, G.; Hahn, M.G.; Keegstra, K.; Raikhel, N.V. Arabidopsis XXT5 gene encodes a putative alpha-1,6-xylosyltransferase that is involved in xyloglucan biosynthesis. Plant J. 2008, 56, 101–115. [Google Scholar] [CrossRef]
- Gille, S.; Pauly, M. O-acetylation of plant cell wall polysaccharides. Front. Plant Sci. 2012, 3. [Google Scholar] [CrossRef]
- Pena, P.J.; Kong, Y.; York, W.S.; O’Neill, M.A. A galacturonic acid-containing xyloglucan is involved in Arabidopsis root hair tip growth. Plant Cell 2012, 24, 1–14. [Google Scholar] [CrossRef]
- Wang, T.; Zabotina, O.; Hong, M. Pectin-cellulose interactions in the Arabidopsis primary cell wall from two-dimensional magic-angle-spinning solid-state nuclear magnetic resonance. Biochemistry 2012, 51, 9846–9856. [Google Scholar] [CrossRef]
- Vogler, H.; Draeger, C.; Weber, A.; Felekis, D.; Eichenberger, C.; Routier-Kierzkowska, A.L.; Boisson-Dernier, A.; Ringli, C.; Nelson, B.J.; Smith, R.S.; et al. The pollen tube: A soft shell with a hard core. Plant J. 2012. [Google Scholar] [CrossRef]
© 2013 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).