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Review

Phylogeny and Functions of LOB Domain Proteins in Plants

by
Yuwen Zhang
1,2,†,
Ziwen Li
1,2,†,
Biao Ma
1,2,
Quancan Hou
1,2 and
Xiangyuan Wan
1,2,*
1
Zhongzhi International Institute of Agricultural Biosciences, Biology and Agriculture Research Center, University of Science and Technology Beijing, Beijing 100024, China
2
Beijing Engineering Laboratory of Main Crop Bio-Tech Breeding, Beijing International Science and Technology Cooperation Base of Bio-Tech Breeding, Beijing Solidwill Sci-Tech Co., Ltd., Beijing 100192, China
*
Author to whom correspondence should be addressed.
†
These authors contributed equally to this work.
Int. J. Mol. Sci. 2020, 21(7), 2278; https://doi.org/10.3390/ijms21072278
Submission received: 15 February 2020 / Revised: 22 March 2020 / Accepted: 23 March 2020 / Published: 26 March 2020
(This article belongs to the Special Issue Plant Genetics and Molecular Breeding)
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Abstract

:
Lateral organ boundaries (LOB) domain (LBD) genes, a gene family encoding plant-specific transcription factors, play important roles in plant growth and development. At present, though there have been a number of genome-wide analyses on LBD gene families and functional studies on individual LBD proteins, the diverse functions of LBD family members still confuse researchers and an effective strategy is required to summarize their functional diversity. To further integrate and improve our understanding of the phylogenetic classification, functional characteristics and regulatory mechanisms of LBD proteins, we review and discuss the functional characteristics of LBD proteins according to their classifications under a phylogenetic framework. It is proved that this strategy is effective in the anatomy of diverse functions of LBD family members. Additionally, by phylogenetic analysis, one monocot-specific and one eudicot-specific subclade of LBD proteins were found and their biological significance in monocot and eudicot development were also discussed separately. The review will help us better understand the functional diversity of LBD proteins and facilitate further studies on this plant-specific transcription factor family.

1. The Confusion in Understanding Functional Diversity of LBD Proteins

Proteins containing conserved Lateral Organ Boundaries (LOB) domain(s) are defined as LOB-domain (LBD) proteins. They are plant-specific transcription factors, existing in plant genomes from green algae to angiosperms. LBD proteins are comprised of a relatively conserved N-terminal region and a variable C-terminal region [1]. The N-terminal region includes an LOB domain that comprises a zinc finger-like motif (CX2CX6CX3C) for DNA-binding activity, a GAS block (Gly-Ala-Ser) and a leucine-zipper-like coiled-coil motif (LX6LX3LX6L) responsible for protein dimerization [2,3]. A conserved proline residue in the GAS block was revealed to play a critical role in the biological function of LBD proteins in Arabidopsis [4]. C-terminal region confers transcriptional activation/repression of target gene expression [5]. According to sequence similarities and phylogenetic analyses, LBD family members were classified into two subfamilies (Class I and Class II) [6,7]. Class I LBD proteins containing zinc finger-like motifs, GAS blocks and leucine-zipper-like coiled-coil motifs can be grouped into four clades (IA, IB, IC and IE), whereas Class II LBD proteins lacking intact leucine-zipper-like domain are divided into two clades (IIA and IIB) [6,7].
LBD proteins were originally thought to play key roles in lateral organ development in plants (systematically reviewed in [3], and partly summarized for root development in [8,9,10,11] and leaf development in [12]), based on which the gene names were determined. However, subsequent progresses in functional studies proved that LBD proteins not only serve as essential transcription factors to regulate plant organ development, but also play important roles in versatile functions during plant growth and development (systematically reviewed in [13] and partly summarized for plant defense in [14]), such as photomorphogenesis [15], pulvinus identity and petiole development [16,17,18], pathogen resistance [19,20,21], hormone response [9,22,23], metabolism regulation [24,25], and heading date [26]. Though the functional significance of LBD proteins has been well summarized in several reviews according to the biological roles in plant development and defense response processes (e.g., root development, leaf development, and plant defense), such diverse functions are still confusing and make it difficult to grasp the regulatory role of this plant-specific gene family encoding transcription factors. One possible reason for the above confusion is that novel functions of LBD proteins have been continuously reported in recent years, while the most fundamental reason is that a method used to effectively sort out function characteristics of LBD proteins is still lacking. By combining the results in functional studies and evolutionary researches of LBD family members, we found that LBD genes have similar molecular functions tending to be in the same phylogenetic clade. It indicates that summarization of LBD gene functions under a phylogenetic framework could effectively resolve the confusion on understanding the diverse functions of LBD proteins. Therefore, to get a comprehensive understanding of such a relatively large family, reviewing functional studies based on deep phylogenetic analysis from more genome-available species is necessary.
Here, we first summarized the classification and evolution of LBD gene family members based on previous reports and generated a newly identified LBD gene family dataset, reconstructing LBD phylogeny from 18 representative genome-available plant species, including four species with evolutionary significance (one kind of green algae, one kind of moss, one kind of fern and one kind of basal angiosperm) and 13 kinds of food and industrial crops (six monocots and seven eudicots), as well as Arabidopsis thaliana (Table 1). We found one monocot-specific and one eudicot-specific LBD protein subclade that were not reported previously. Then, based on functional studies on Arabidopsis LBD proteins and the phylogenetic relationships, conserved and diverse functions of Arabidopsis LBD proteins in each clade were recapitulated. Finally, we summarize and discuss the functions for almost all of the function-reported LBD genes so far (50 genes) according to their phylogenetic classifications. This review closes the gap between functional studies and evolutionary researches on the LBD family. More importantly, through the phylogenetic analyses and clustering analysis, functions of a large number of genes can be predicted to facilitate further research on plant LBD proteins.

2. The Phylogeny of LBD Family Proteins

Genome-wide identification and evolutionary analysis of LBD gene families have been studied in more than a dozen plants [2,27,28,29,30,31,32,33,34,35,36,37]. Given that the genomes of 300 plant species were sequenced (plabiPD database), there remain a considerable number of genome-available species whose LBD genes deserve to be studied at genome level. In order to explore the functions of LBD proteins in more species, here a sophisticated method was used to identify the LBD genes in 18 genome-available species. Eight representative protein sequences from Arabidopsis and maize were used as queries to perform BLASTP searches against genome-wide predicted protein sequences of 18 genome-available plant species spanning from charophyta to angiosperms (Table 1). All candidate LBD protein sequences were examined by domain analysis using Pfam (http://pfam.xfam.org/) [38] with the default cut-off parameters. Only proteins with matched sequences covering at least 70% length of the complete LOB domain were regarded as LBD proteins. All the identified 823 LBD protein sequences used to reconstructed the phylogenetic tree shown in Figure 1 are provided in Supplementary Additional file 1.
Previous phylogenetic analyses of LBD genes indicate that they constitute a green plant-specific gene family that may have originated during the early evolution of charophyte algae [7]. Using the identified 823 LBD proteins from 18 plant species and nine well-studied LBD proteins from other species, we reconstructed a phylogenetic tree. Consistent with previously published topology results [6,7,39], LBD proteins can be classified into two major classes, Class I and Class II. Genes in Class I can be further grouped into four clades, Class IA (IA1-1, IA1-2, IA2), Class IB, Class IC (IC1/D-1, IC1/D-2, IC1/D-3 and IC1/D-4, IC2 ) and Class IE, and Class II consists of two clades (IIA and IIB) (Figure 1). This classification also works in LBD proteins from an individual plant (e.g., Arabidopsis).
A previous study had proved that the ancestral LBD proteins of the four clades of Class I and the subfamily Class IIB already exist in the last common ancestor of charophyte algae and land plants [7]. Here, we found LBD proteins from Cylindrocystis brebissonii, which belongs to charophyte algae located basally on the phylogenetic tree (see Figure 1 and some details in Part 4). The C. brebissonii LBD proteins distribute in clades of Class IA, Class IC and subfamily Class II, and each of them has two members. Phylogenetic results here show that C. brebissonii does not have Class IB type of LBD proteins, being consistent with some previous studies that proved that Class IB LBD proteins predominantly function in regulating lateral root development [40,41,42,43,44]. However, one previous comprehensive study demonstrated that LBD genes of charophyte algae are placed in all four clades of the Class I and Class II gene lineages [7], while this conclusion has not been proved by other studies. This may be due to the possibility that some other species belonging to charophyte algae possess Class IB and Class IE clades, and it is also possible that inaccurate sequence usage affected the analysis result. Our results also proved that both Physcomitrella patens and Selaginella moellendorffii have five major branches of LBD genes (Class II and four clades in Class I), which is consistent with the previous study [6]. Accordingly, maybe the initial radiation of the LBD gene family of five major branches was already established before the plants gained real roots. Amborella trichopoda is a known angiosperm that was the earliest one separated from other angiosperms. Its LBD proteins mainly distribute in the Class IA (IA1-2, IA2), Class IB, Class IC (IC1/D-2, IC1/D-4, IC1/D-5, and IC2), Class IE and Class II (IIA, IIB).
In our phylogenetic analyses, LBD proteins of the monocots and eudicots can separated from each other. The LBD proteins of Arabidopsis and maize are distributed in all major clades. However, at subclade level, the Arabidopsis and other eudicots have no protein distribution in the Class IC1/D-3 subclade (Figure 1 and some details in Part 4). Here, this subclade has eight homologs. Both wheat (TraesCS4A02G297500, TraesCS4D02G014600) and maize (Zm00001d013625, Zm00001d033466) have two members in this subclade, while rice (BGIOSGA013249), barley (HORVU4Hr1G002480), Setaria italica (SETIT_037583mg) and sorghum (SORBI_3001G147000) each has one. It indicates that the subclade may be monocot specific and these genes may play important roles in monocot plant development. However, no gene from this subclade has been cloned and investigated so far. Through searching the online databases of MaizeGDB (https://archive.maizegdb.org/) and BAR (http://bar.utoronto.ca/), we found that Zm00001d013625, Zm00001d033466 and BGIOSGA013249 are all highly expressed in shoot apical meristem (SAM). Zm00001d013625 and Zm00001d033466 are highly expressed in V5 stage (five leaves fully emerged) with similar expression patterns. Since the V5 stage is the time point when the stem tip growth point begins to develop the tassel primordia in maize [45], the monocot-specific genes are probably involved in inflorescence architecture development. In contrast, the Class IA1-1 is a eudicot-specific subclade (Figure 1 and some details in Part 4). Among the 14 identified Class IA1-1 genes, four belong to G. max (GLYMA_18G025600, GLYMA_11G231500, GLYMA_14G057600 and GLYMA_02G264500), two belong to each of M. truncatula (MTR_3g071420 and MTR_5g083010) and G. raimondii (B456_011G291500 and B456_013G016900), one belongs to each of A. thaliana (AT3G11090), B. vulgaris (BVRB_2g023440), B. napus (BnaC05g42060D), D. carota (DCAR_011832), S. tuberosum (PGSC0003DMG400027718) and LjLOB1 from Lotus japonicus. LjLOB1 was identified with strong expression at the bases of leaflet primordia, suggesting a potential function in leaf development of eudicots [46]. Taken together, both monocots and eudicots have their specific subclades. It may be generated from recent gene duplication events that occurred after dicot and monocot separation or result from gene loss events in the other evolutionary clade when dicots and monocots are separated.

3. Functional Conservation and Diversity of LBD Proteins in Arabidopsis

Arabidopsis, as a model plant, has the most in-depth studies on the functions of LBD genes. In Arabidopsis, the LBD gene family comprises 43 members, and at least 25 of them have been cloned and functionally characterized [3,13,47,48,49]. Here, we summarize the recent progress on the identification and characterization of LBD proteins in Arabidopsis and, combining the reported LBD gene functions with the phylogenetic results of Arabidopsis LBD family members, further investigate the substantial relationship between phylogenetic homology and functional similarity of LBD family genes.
By combining the function reports and evolutionary relationship of Arabidopsis LBD proteins, we found that LBD genes in the same phylogenetic clade tend to have similar molecular functions (Figure 2). Class IA Arabidopsis LBD proteins have main functions in aboveground organs (leaf adaxial–abaxial polarity and plant reproduction). Class IB LBD proteins play primary roles in the development of underground organs (lateral root formation). Class II LBD proteins mainly regulate anthocyanin synthesis and nitrogen responses. Molecular roles of Class IC and Class IE LBD proteins cannot be simply summarized due to the limited functional reports. Therefore, at least three of the five evolutionary branches of LBD proteins can be summarized in molecular functions under the phylogenetic framework. It is an effective strategy to resolve the confusion in understanding the functional diversity of LBD family members and can be used to reviewing the regulatory roles of LBD proteins.

4. Function Summarization Under Phylogenetic Framework

LBD genes were identified from many genome-available plant species, including Arabidopsis [2], rice [36], poplar [37], tomato [27], Malus domestica (apple) [28], Medicago truncatula [29], maize [30], grape [31], mulberry [32], barley [33], Camellia sinensis [34] and Eucalyptus grandis [35], with gene family sizes ranging from 24 to 58 genes. Recently, several studies focused on LBD protein identification and their novel roles are reported [26,50,51,52,53]. However, a large number of LBD proteins are still unexplored. So far, at least 50 LBD genes have been characterized to be involved in various processes of plant development and metabolism. A brief summary of these reported LBD genes is in Table 2. Arabidopsis was a model for the most in-depth studies on the function of the LBD gene family (25 LBD genes in Table 2). Besides, functions of some LBD proteins from other plant species were also investigated, including 10 in rice [3,13,26,53,54,55], four in maize [5,41,56,57], three in L. japonicus [16,46], two each in M.truncatula [16,58] and E. grandis [35], one in each of the five species (wheat [1], H. vulgare [50], citrus [20], pea [16] and apple [28]) (Table 2). In the next section, we summarize and discuss the major reports on the identification and characterization of LBD proteins in Arabidopsis and other plant species according to the reconstructed phylogenetic relationships.

4.1. Functions of LBD Proteins in Class IA Clade

In Class IA1-1 subclade, we identified only one characterized member, LjLOB1, from L. japonicus (Table 2). In Class IA1-2 subclade, there are 10 LBD proteins in Arabidopsis, and six of them were functionally characterized (AtLOB, AtLBD25/AtDDA1, AtLBD6/AS2, AtLBD36/AS1, AtLBD10 and AtLBD28) ( Figure 2 and Figure 3, Table 2).
AtLOB is one of the earliest identified members (founding members) of LBD proteins in A. thaliana. AtLOB loss-of-function mutant exhibits organ fusions under standard growth conditions [60]. Ectopic expression of AtLOB altered the size and shape of leaves, adaxial–abaxial polarity, and caused male and female sterility due to abnormal floral organs, suggesting its potential role in lateral organ development [2]. AtLOB can directly target the promoter region of PHYBACTIVATION TAGGED SUPPRESSOR1 (BAS1) to negatively regulate brassinosteroid accumulation, resulting in limited growth in organ boundaries [59,60]. A basic helix-loop-helix (bHLH) member bHLH048 can interact with AtLOB and the interaction results in reduced affinity of AtLOB for the consensus DNA motif, which suggest that bHLH048 post-translationally regulates the function of AtLOB at lateral organ boundaries [61]. Another Class IA1-2 protein AtDDA1 is reported to play a role in photomorphogenesis through regulating light/dark-dependent hypocotyl elongation [15]. AtDDA1 is expressed primarily in vascular tissues and its abundance is repressed by auxin and darkness treatments [15]. The dda1-1 mutant, a conditional gain-of-function and semi-dominant allele, had a diminished auxin response and displayed aberrant hypocotyl elongation in the dark [15].
Three orthologous genes of AtLOB were identified in monocots, including ramosa2/ra2 in maize, HvRA2 in barley and OsRA2 in rice (Table 2). The maize ra2 is expressed at the axillary meristem initiation sites of the inflorescences and is involved in floral development [56,89]. In barley, HvRA2 is a central player in establishing the inflorescence architecture of spikes, as well as in determining yield potential and grain number [50]. In rice, OsRA2 was identified to regulate seed morphology and pedicel development in the panicle [54]. Moreover, OsRA2 acts downstream of RCN2 in regulating pedicel and branch lengths, but upstream of RCN2 for control of the number of secondary branches. This indicates that branch number and length in the panicle are separately regulated by OsRA2 through parallel pathways [54]. Additionally, sequence alignment of RA2-like with other LBD proteins reveals a grass-specific domain that is not found in A. thaliana in the C-terminus [56]. The expression pattern of RA2 is conserved in rice, barley and maize, suggesting that RA2 may be a common factor critical for shaping the initial steps of grass inflorescence architecture [56]. Recently, crystal structural analysis of the LOB domain of wheat Ramosa2 reveals that RA2 shares some features different from other LBD proteins, and this study contributes to establish an atomic-scale mechanistic model for LBD proteins as transcriptional regulators in plants [1].
For eudicots, ELP1/PLP in M. truncatula, APU in pea (Pisum sativum), SLP and LjLOB3 in L. japonicus also belong to Class IA1-2 (Table 2). Among them, ELP1, APU and SLP are orthologous proteins of AtLOB and were identified to regulate nastic leaf movement. Nastic leaf movement is generated by pulvinus and/or pulvinula, which are specialized motor organs located at the base of the petiole and petiolulae [90]. In M. truncatula, ELP1/PLP is specifically expressed in the pulvinus that gives rise to the motor organ [16]. The ELP1/PLP loss-of-function mutants in M. truncatula were impaired in pulvinus differentiation and failed to fold its leaflets in the dark [16,17]. Ectopic expression of ELP1/PLP resulted in dwarf plants with reduced petiole and rachises length, and the epidermal cells gained characteristics of motor organ epidermal cells [16]. The orthologs of ELP1/PLP in other legume species, including APU in pea and SLP in L. japonicas, confer similar regulation of pulvinulae development by a conserved molecular mechanism [16,17]. Furthermore, ELP1/PLP can be negatively regulated by PHANTASTICA (MtPHAN), as MtPHAN is required to maintain petiole identity by repressing the ectopic expression of ELP1 [18]. In addition, LjLOB3 was strongly expressed at the bases of leaflet primordia, suggesting its potential function in leaf development in L. japonicus [46].
In Arabidopsis, AtLBD6/AS2, AtLBD36/AS1, AtLBD10 and AtLBD28 are classified into Class IA2 subclade (Figure 2, Table 2). AS2, the other founding member of LBD gene family, can form complexes with different proteins to regulate various aspects of plant growth and development [62,63,64,65]. AS2 physically associates with AS1 to form a repressor complex that regulates the polarity and morphologies of leaf, the inflorescence architecture and fertility, and the differentiation of shoot apical meristem [62,63,64,65]. AS2 interacts with AtLBD30/JLO to regulate the expressions of several PIN-FORMED (PIN) genes encoding Aux efflux facilitators [80,91,92]. AS2, AS1 and JLO can form a trimeric protein complex involved in organ boundary establishment via the negative regulation of KNOX gene expression [66]. In addition, AS2 alone can promote gibberellin (GA) synthesis via repression of KNOX gene [93]. AtLBD28 might affect the polarity and morphologies of leaf and the differentiation of shoot apical meristem [47]. However, AtLBD10 has a unique biological function different from the other three well-studied members. It is involved in microspore polarization prior to the first asymmetric division, as well as in germ cell mitosis [68,69]. The lbd10 mutants had aborted pollen grains at a ratio of 12.7%, indicating that AtLBD10 is important for Arabidopsis pollen development [68].
In other plants, OsAS2 and OsIG1 in rice, IG1 in maize, TaAS2 in wheat and MdLBD11 in M. domestica are all classified into Class IA2 subclade (Table 2), and they are orthologous proteins of Arabidopsis AS2. OsIG1 can regulate shoot differentiation and leaf development [70], and the development of floral organs and megagametophyte in rice [71]. The maize IG1 was characterized as a key regulator of leaf adaxial–abaxial patterning, as well as embryo sac development. Furthermore, mutant of ig1 leads to male sterility in some genetic backgrounds (A158, W23, W64A and W22) and variable male sterility in other genetic background (Mo17) [57]. Ectopic expression of wheat TaAS2 in Arabidopsis leads to the adaxialization of abaxial mesophyll tissues and alterations of the vascular patterns in leaves and petioles [72]. The M. domestica MdLBD11 was highly similar to Arabidopsis AS1 and AS2 in molecular functions in regulating leaf and flower development. Overexpression of MdLBD11 in Arabidopsis resulted in upward curling leaves, delayed flowering, downward pointing flowers and abnormal siliques and other phenotypic changes [28].
Taken together, 19 LBD proteins in Class IA clade were identified from nine plant species. Most of the Class IA members function in aboveground organ development, including the differentiation of SAM, the size, shape and adaxial–abaxial polarity of leaves, inflorescence architecture, pollen development, pulvinus development, nastic leaf movement, and photomorphogenesis process. Though some genes were identified in other plants, the functions of their homologous genes in our selected six monocots and eight eudicots are still unclear. In order to get a clear phylogenetic relationship between well-studied and function-unknown genes, a more detailed phylogenetic tree for Class IA clade is shown (Figure 3), based on which functions of uninvestigated genes belonging to listed species in the phylogeny can be predicted by taking their well-studied homologs as references.

4.2. Functions of LBD Proteins in Class IB Clade

In Arabidopsis, 10 LBD proteins are classified into Class IB clade, nine of which have been characterized (Figure 2, Table 2). Their functions are mainly involved in root development, callus formation and differentiation of tracheary elements, and the resistances to Fusarium oxysporum and root-knot nematode (RKN) pathogenesis.
LBD genes play important roles in regulating root development. They regulate lateral root (LR) formation in Arabidopsis [43,49,73] and Medicago [58], crown root (CR) [42] and adventitious root (AR) [84] development in rice, and shoot-borne root initiation in maize [5,41,85]. In Arabidopsis, AtLBD16, AtLBD18, AtLBD29 and AtLBD33 genes act downstream of ARF7/19-mediated auxin signal transduction cascade to control the LR formation [40,44,75,93,94,95,96] (Figure 2, Table 2). AtLBD29 was expressed in the LR primordia [40], AtLBD16 was expressed throughout the young LR [44,97], and expression of AtLBD18 was restricted to the base of the LR [44]. AtLBD18 forms a heterodimer with AtLBD33 to reactivate the auxin-dependent division [76]. It was shown that the auxin influx carriers AUXIN1 (AUX1) and LIKE-AUXIN3 (LAX3) are required for the auxin-induced expression of AtLBD16 and AtLBD18 to control LR development during various stages in Arabidopsis [98,99,100]. The ARF7/19-AtLBD16/18 transcriptional module was also identified as playing an important role in AR formation in Arabidopsis [101]. In Arabidopsis, initiation of LR formation starts from the founder cells’ asymmetric division, and through subsequent cell proliferation and differentiation to form new primordia. AtLBD16 is a key member for LR formation in an auxin-dependent manner [11,102]. LR initiation requires the sequential induction of transcription factor gene AtLBD16 and its target PUCHI [102]. AtLBD18 and ARFs form a double positive feedback loop, as AtLBD18 can not only bind to the ARF19 promoter directly but also interacts with ARF7 and ARF19 [101]. These feedback loops may contribute to the continued LR growth in response to auxin in Arabidopsis [101]. The coiled-coil motifs in AtLBD16 and AtLBD18 transcription factors determine their DNA-binding properties, including DNA-binding diversity, specificity and affinity, which functions in the transcriptional regulation of different cellular processes and biological pathways in Arabidopsis [103]. By contrast, AtLBD14 was not responsive to auxin, but it was downregulated by ABA and participates in ABA-mediated regulation of LR formation [51,73] (Figure 2, Table 2).
Callus formation, the initial step of the typical in vitro plant regeneration triggered by auxin, shares a similar genetic pathway with LR development [104,105]. In Arabidopsis, the LBD proteins that control LR formation, such as AtLBD16, AtLBD17, AtLBD18, and AtLBD29 (Figure 2, Table 2), were identified as key regulators of callus induction in various organs, but the molecular mechanisms of auxin-induced callus formation remain largely elusive [74]. Recently, it was shown that Arabidopsis basic region/leucine-zipper-motif 59 (AtbZIP59) transcription factor forms complexes with LBD proteins to modulate auxin-induced callus formation [52]. Auxin can stabilize AtbZIP59 and enhance its interaction with AtLBD16, and AtbZIP59–LBD16 complex directly targets an FAD-binding Berberine (FAD-BD) gene’s promoter and regulates its transcription [52]. Furthermore, the WOX11-LBD16 pathway was proved to promote pluripotency acquisition in callus cells [106]. Using ChIP sequencing (ChIP-seq) and RNA sequencing (RNA-seq) approaches, more than 350 target genes of AtLBD29 were identified participating in the regulation of cell reprogramming during callus formation. AtLBD29 rapidly activates genes that are involved in reactive oxygen species (ROS) and lipid metabolism, methylation and cell wall hydrolysis, but suppresses most of the light-responsive genes [78]. Besides, a recent study suggests that AtLBD19 may play an important role in coordinating callus formation in Arabidopsis along with other AtLBD members [77]. Moreover, AtLBD16 and AtLBD29 are required for AR formation from wounded or detached plant tissues, a different auxin-driven process called “de novo root organogenesis” [105]. WOX11 acts redundantly with its homolog WOX12 and directly responds to a wounding-induced auxin that accumulated in and surrounding the procambium to activate AtLBD16 and AtLBD29 expressions, which lead to the first step in cell fate transition from a leaf procambium or its nearby parenchyma cell to a root founder cell [105].
JAGGED LATERAL ORGANS (JLO) is a dosage-dependent regulator of cell specification and organ patterning throughout plant development [66,79,91] (Table 2). Loss of JLO resulted in arrested seedling development at early stages and even embryo lethality [79,91], while compromised JLO activity leads to abnormal organ initiation and patterning of leaf and flower [66]. AS1, AS2, and JLO form a trimeric protein complex to involve in the formation of organ boundaries by negatively regulating KNOX expression [66]. JLO transcriptionally regulates several PIN genes (encoding auxin efflux facilitators) independently or together with AS2 [79,91,92]. JLO also coordinates root meristem identity through activating AP2 transcription factors (encoded by PLT genes) that further regulate PIN expression [91,107,108]. In addition, JLO is involved in hypophysis specification and primary root meristem formation during embryogenesis by influencing the action of the auxin-signaling module BDL/IAA12-MP/ARF5 [91]. The versatile functions of JLO in plant development are probably due to its involvement in regulating auxin distribution and signaling [13]. Besides, JLO and AtLBD18 are recently duplicated genes involved in the differentiation of tracheary elements of xylem vessels via the positive feedback regulation of NAM/ATAF/CUC (NAC) proteins [76,109].
In addition to the functions in plant development, some Class IB clade members of Arabidopsis also play important roles in response to fungal pathogens and soil nematodes [14]. AtLBD20, a predominantly root-expressed LBD gene in Arabidopsis, is a negative regulator of both F. oxysporum resistance and a subset of jasmonic acid (JA) responses [19]. Loss-of-function mutants of Atlbd20 display increased resistance to the root-infecting vascular wilt pathogen F. oxysporum, indicating that AtLBD20 acts as a negative regulator of JA-regulated pathogen defense. Besides, AtLBD16 is regulated by auxin in galls and induced by nematode secretions (including auxin compounds and can trigger changes in pericycle cells through inducing the expression of AtLBD16) [21]. AtLBD16 and its co-regulated genes integrate the auxin signaling cascades in both LR and callus formation, establishing the molecular links between lateral root development and RKN pathogenesis [110] (Figure 2, Table 2). Furthermore, beet necrotic yellow vein virus (BNYVV) can hijack some auxin-regulated pathways that are dependent on several LBD transcription factors to cause rhizomania of sugar beet [111]. Therefore, Class IB clade LBD genes are crucial molecular targets for plant pathogen invasion.
For other plants, five LBD genes have been characterized (Table 2 and Figure 4). LBD genes Crl1 (Arl1) and OsARL1 in rice are involved in the formation of monocot-specific CR and AR, respectively [42,82,83,84]. The Crl1 orthologs in maize, RTCS and RTCL, are responsive to auxin and regulate in embryonic seminal and post-embryonic shoot-borne root initiation [5,41,85]. OsDH1, the first reported LBD gene with tissue-specific and temporal expression patterns, is involved in rice floral organ development [81]. In L. japonicus, LjLOB4 was expressed at the boundaries between whorls in developing floral buds, suggesting a potential function during floral development [46].
Taken together, most of the Class IB clade members are involved in auxin-related biological processes, including root development, differentiation of tracheary elements, callus formation, root-related resistance to plant pathogen, and the development of leaves and flowers. A more detailed phylogenetic tree was reconstructed from Class IB LBD proteins in 18 plant species, facilitating the further research on the functions of unknown members (Figure 4).
Interestingly, as mentioned above, Class IA LBD proteins mainly function in the regulation of aboveground organs; contrarily, a set of Class IB members regulate root development and root-related biological processes. In order to find the sequence difference potentially responsible for the functional diversities between Class IA and Class IB LBD genes, representative protein sequences from the two clades were compared in the LOB domains (Figure 5). At some positions (highlighted with red frames), amino acid residues are conserved within each of the two classes but are divergent between them. Amino acids at these positions may determine the specificity of target genes and explain functional differences between the two classes of LBD genes in regulating the aboveground and the below-ground organ development, respectively.

4.3. Functions of LBD Proteins in Class IC Clade

In Arabidopsis, four out of 11 Class IC LBD proteins (AtLBD3, AtLBD12, AtLBD13 and AtLBD15) were characterized (Figure 2, Table 2). AtLBD3 and AtLBD12 belong to subclade IC1/D, while AtLBD13 and AtLBD15 belong to subclade IC2. AtLBD3 is expressed at the base of shoot lateral organs and root, and it is temporally and spatially regulated by the plant hormone cytokinin in a manner dependent on the His-Asp phosphorelay signal transduction [23]. AtLBD3 overexpression transgenic lines commonly display a dwarfism phenotype with stunted rosette leaves, inflorescences and flowers [23]. AtLBD12 is involved in the growth of abaxial leaf surface, apical dominance and fertility as identified by using an activation tagging line [86]. The expression of AtLBD13 is not responsive to auxin and ABA, but can be downregulated by brassinolide treatment, which indicates that AtLBD13 may have a unique role in lateral root formation [49]. AtLBD15 is involved in SAM development through regulating WUSCHEL (WUS) expression and affecting xylem establishment [48,87].
In rice, LBD12-1 loss-of-function mutant had a larger SAM under salt stress, whereas overexpression of LBD12-1 resulted in reduced SAM size through repressing AGO10 expression [53]. OsLBD3-7 is involved in the regulation of rice leaf rolling as its overexpression leads to narrow and adaxially rolled leaves [55]. In citrus, CsLOB1, the ortholog of AtLBD1 and AtLBD11, is a general susceptibility gene for citrus bacterial canker (CBC) disease incited by multiple Xanthomonas species [20]. In E. grandis, two Class IC LBD proteins were identified. Overexpressing EgLBD37 leads to the significant increase of secondary xylem, and overexpressing EgLBD29 results in greatly increased phloem fiber production [35], which suggests that E. grandis LBD genes may play important roles in secondary growth (Table 2).
Collectively, the Class IC clade LBD proteins mainly regulate cytokinin-mediated plant growth, abaxial surface of leaves, apical dominance, fertility, and secondary growth. A more detailed phylogenetic tree of Class IC LBD proteins was reconstructed for future researches (Figure 6).

4.4. Functions of LBD Proteins in Class IE Clade

Among Class IE LBD members, only Arabidopsis AtLBD27 was functionally studied (Figure 2, Table 2). AtLBD27 plays an essential role in pollen development [68,69,112]. Flowering plants have a complex life cycle that involves a switch between a multicellular (2n) sporophyte generation and a (n) gametophyte generation. AtLBD27 is required for correct initiation and orientation of the polarized microspore’s asymmetric division to generate bicellular pollen, as the lbd27 mutant produces aberrant microspores with increased cell expansion, delayed mitosis entry and altered nuclear division orientation phenotypes. [112,113]. AtLBD10, which belongs to Class IA, can also affect the pollen development as mentioned above. The lbd10 or lbd27 single mutant had aborted pollen grains at a ratio of 12.7% and 70% respectively, whereas all pollens in the lbd10 lbd27 double mutants were aborted, indicating that both AtLBD10 and AtLBD27 are essential for Arabidopsis pollen development [68]. Figure 7 shows a more detailed phylogenetic tree for Class IE clade LBD proteins.

4.5. Functions of LBD Proteins in Class II Clade

There are six Arabidopsis LBD proteins in the Class II clade and they can be further divided into two subclades, Class IIA and Class IIB (Figure 2 and Figure 8, Table 2). In Arabidopsis, two of Class IIA LBD proteins (AtLBD40 and AtLBD41) were functionally studied. AtLBD40 is reported to be downregulated by GA but upregulated by DELLA proteins [22]; however, no more detailed analysis of this gene is available at present. AtLBD41 was detected in the adaxial and internal domain between the ab-adaxial domains of leaves, indicating it might play a role in the specialization of adaxial cells in Arabidopsis lateral organs [88]. Up to now, there is no more to report about Class IIA members in other plants.
For Class IIB, three members (AtLBD37, AtLBD38 and AtLBD39) were identified in Arabidopsis, with main functions in anthocyanin synthesis and nitrogen (N) metabolism (Figure 8). N and nitrate (NO3-) can regulate many aspects of plant metabolism, growth, and development. In Arabidopsis, N and NO3- suppress anthocyanin synthesis via the induction of AtLBD37, AtLBD38 and AtLBD39 expressions [24,114]. The three LBD genes act as repressors of N availability signals by negatively regulating two anthocyanin synthesis regulators (PAP1 and PAP2) and N-responsive genes [24]. Recent studies reported that AtLBD37 can interact with the development regulators of TPL/TPR proteins and miP1a/b/TPL complex to repress flowering by recruiting CONSTANS (CO, a potent regulator of flowering time) [115,116].
For other plants, three Class IIB LBD proteins were identified, including two from rice and one from Medicago (Figure 8, Table 2). In rice, the metabolomic and transcriptomic analysis on OsLBD37 overexpressing plants revealed that OsLBD37 is also associated with nitrogen metabolism [25]. OsLBD37 and OsLBD38, two homologs of Arabidopsis AtLBD37, serve as negative regulators of rice heading date [26]. Overexpression of OsLBD37 and OsLBD38 delayed heading date and increased yield via downregulating the florigen genes Hd3a and RFT1 and the key regulator of heading date Ehd1 [26]. In Medicago, homeobox 1 (HB1, belonging to the HD-Zip family) directly binds to a CAATAATTG cis-element present in the promoter of LBD1 to regulate the LR emergence by auxin [58]. Figure 8 shows a more detailed phylogenetic tree for Class II clade LBD proteins.

5. Conclusions and Perspectives

LBD proteins, a family of plant-specific transcription factors, play important roles in controlling plant development and responding to external stimuli. In this review, we identified 823 LBD proteins from 18 high-quality plant genomes containing green algae (C. brebissonii), moss (P. patens), fern (S. moellendorffii), and angiosperms (A. trichopoda, eight eudicots and six monocots). The phylogenetic results are mainly consistent with previous studies. However, through detailed analyses of the proteins from different branches, we found the Class IC1/D-3 subclade is specific to monocots and Class IA1-1 subclade is specific to eudicots. All the eight LBD proteins in Class IC1/D-3 subclade are from monocots, and three genes Zm00001d013625, Zm00001d033466 and BGIOSGA013249 are all highly expressed at the time point when the stem tip growth point begins to develop the tassel primordia. Thus, the Class IC1/D-3 subclade may be involved in the biological process of inflorescence architecture development. The Class IA1-1 is specific for eudicots and only one gene in this clade has been functionally investigated with strong expression at the bases of leaflet primordia, indicating that the subclade may play important roles in eudicot leaf development. Therefore, it would be interesting to precisely identify the functions of LBD proteins in Class IC1/D-3 and Class IA1-1 to explore whether these proteins are key regulators in determining morphogenesis.
We summarize the characterized gene functions based on a phylogenetic framework, which effectively facilitates understanding of diverse functions of LBD family proteins. We found Class IA is mainly involved in regulating the development of aboveground organs (leaves, stems, flowers) and their related biological and abiotic reactions (inflorescence architecture and photomorphogenesis). Class IB is mainly involved in regulating the development of underground organs (lateral roots, crown roots and adventitious roots) and their related biological processes (root-related plant diseases and insect pest responses). The subclade Class IIB LBD proteins are mainly involved in nitrogen metabolism in Arabidopsis and rice. The number of well-studied genes in Class IC and Class IE is small and their molecular mechanism in transcriptional regulation is still unknown. At present, the majority of well-studied LBD proteins belong to Arabidopsis, and few LBD proteins are characterized in other plants. Therefore, one major task for further studies is to investigate LBD gene functions in other plants, and another one is to characterize individual LBD proteins by elucidating their regulatory mechanisms and involved pathways, such as disclosing cis-regulatory elements, identifying protein partners, and detecting downstream targets and upstream regulators.

Supplementary Materials

Supplementary materials can be found at https://www.mdpi.com/1422-0067/21/7/2278/s1. Additional file 1. LBD proteins of four other plants; Additional file 2. LBD proteins of six monocots; Additional file 3. LBD proteins of eight eudicots; Additional file 4. LBD protein sequences

Author Contributions

X.W. conceived the review. Y.Z., Z.L., B.M. and Q.H. wrote and revised the review. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the National Key Research and Development Program of China (2017YFD0102001, 2018YFD0100806, and 2017YFD0101201), the National Transgenic Major Program of China (2018ZX0800922B and 2018ZX0801006B), the National Natural Science Foundation of China (31771875 and 31871702), the Fundamental Research Funds for the Central Universities of China (06500060, FRF-TP-18-013A1, FRF-TP-18-014A1), the “Ten Thousand Plan”-National High Level Talents Special Support Plan (For Xiangyuan Wan) and the Beijing Talents Foundation (No. 2016000021223TD04).

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. The phylogeny of LBD proteins in 18 genome-available plant species. The phylogenetic tree was reconstructed using aligned amino acid sequences of LOB domains. We reconstructed the hidden Markov model (HMM) of LBD domain using hmmbuild (HMMer package) with 163 seed sequences belonging to the LBD gene family (PF03195) in the Pfam database. All collected protein sequences of LBD candidates were aligned to the above HMM LBD domain by hmmalign (HMMer package). A maximum likelihood (ML) tree was constructed using the PhyML program with JTT model and 100 times of bootstrap replicates. Colored taxon names indicate the presence of Class IA1 (IA1-1, IA1-2) (blue), Class IA2 (orange), Class IB (yellow), Class IC1/D (IC1/D-1, IC1/D-2, and IC1/D-4)(cyan) without IC1/D-3 (black), Class IC2 (purple), Class IE (green), Class IIA (black) and Class IIB (red).
Figure 1. The phylogeny of LBD proteins in 18 genome-available plant species. The phylogenetic tree was reconstructed using aligned amino acid sequences of LOB domains. We reconstructed the hidden Markov model (HMM) of LBD domain using hmmbuild (HMMer package) with 163 seed sequences belonging to the LBD gene family (PF03195) in the Pfam database. All collected protein sequences of LBD candidates were aligned to the above HMM LBD domain by hmmalign (HMMer package). A maximum likelihood (ML) tree was constructed using the PhyML program with JTT model and 100 times of bootstrap replicates. Colored taxon names indicate the presence of Class IA1 (IA1-1, IA1-2) (blue), Class IA2 (orange), Class IB (yellow), Class IC1/D (IC1/D-1, IC1/D-2, and IC1/D-4)(cyan) without IC1/D-3 (black), Class IC2 (purple), Class IE (green), Class IIA (black) and Class IIB (red).
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Figure 2. Phylogeny and functions of Arabidopsis LBD proteins. The phylogenetic tree was reconstructed in MEGA6 using aligned protein sequences of LOB domain regions in Arabidopsis by ML method with JTT model and Nearest-Neighbor-Interchange (NNI) heuristic searches based on an NJ (neighbour-joining) initial tree. Support values (>30) are shown next to the nodes. The colors of branches and gene names correspond to those in Figure 1.
Figure 2. Phylogeny and functions of Arabidopsis LBD proteins. The phylogenetic tree was reconstructed in MEGA6 using aligned protein sequences of LOB domain regions in Arabidopsis by ML method with JTT model and Nearest-Neighbor-Interchange (NNI) heuristic searches based on an NJ (neighbour-joining) initial tree. Support values (>30) are shown next to the nodes. The colors of branches and gene names correspond to those in Figure 1.
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Figure 3. Phylogeny of LBD proteins from Class IA in 18 species. This phylogeny was reconstructed using Class IA LBD proteins identified in Figure 1 and according to the same method described in Figure 1 legend. “*” means functionally characterized LBD protein in Table 2 (Gene ID is in brackets for LBD proteins of 18 species, species name is in square brackets for LBD proteins of other species). LBD proteins of eudicots, monocots, and other plant species are marked in red, blue and black, respectively. Branch color corresponds to that in Figure 1.
Figure 3. Phylogeny of LBD proteins from Class IA in 18 species. This phylogeny was reconstructed using Class IA LBD proteins identified in Figure 1 and according to the same method described in Figure 1 legend. “*” means functionally characterized LBD protein in Table 2 (Gene ID is in brackets for LBD proteins of 18 species, species name is in square brackets for LBD proteins of other species). LBD proteins of eudicots, monocots, and other plant species are marked in red, blue and black, respectively. Branch color corresponds to that in Figure 1.
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Figure 4. Phylogeny of LBD proteins from Class IB in 18 species. This phylogeny was reconstructed using Class IB LBD proteins identified in Figure 1 and according to the same method described in Figure 1 legend. “*” means functionally characterized LBD protein in Table 2 (Gene ID is in brackets for LBD proteins of 18 species, species name is in square brackets for LBD proteins of other species). LBD proteins of eudicots, monocots, and other plant species are marked in red, blue and black, respectively. Branch color corresponds to that in Figure 1.
Figure 4. Phylogeny of LBD proteins from Class IB in 18 species. This phylogeny was reconstructed using Class IB LBD proteins identified in Figure 1 and according to the same method described in Figure 1 legend. “*” means functionally characterized LBD protein in Table 2 (Gene ID is in brackets for LBD proteins of 18 species, species name is in square brackets for LBD proteins of other species). LBD proteins of eudicots, monocots, and other plant species are marked in red, blue and black, respectively. Branch color corresponds to that in Figure 1.
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Figure 5. Sequence comparison of selected Class IA and Class IB LBD proteins. Red frame indicates conserved amino acid residue within each clade. “*” indicates conserved amino acid residues across different clades.
Figure 5. Sequence comparison of selected Class IA and Class IB LBD proteins. Red frame indicates conserved amino acid residue within each clade. “*” indicates conserved amino acid residues across different clades.
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Figure 6. Phylogeny of LBD proteins from Class IC in 18 species. This phylogeny was reconstructed using Class IC LBD proteins identified in Figure 1 and according to the same method described in Figure 1 legend. “*” means functionally characterized LBD protein in Table 2 (Gene ID is in brackets for LBD proteins of 18 species, species name is in square brackets for LBD proteins of other species). LBD proteins of eudicots, monocots, and other plant species are marked in red, blue and black, respectively. Branch color corresponds to that in Figure 1.
Figure 6. Phylogeny of LBD proteins from Class IC in 18 species. This phylogeny was reconstructed using Class IC LBD proteins identified in Figure 1 and according to the same method described in Figure 1 legend. “*” means functionally characterized LBD protein in Table 2 (Gene ID is in brackets for LBD proteins of 18 species, species name is in square brackets for LBD proteins of other species). LBD proteins of eudicots, monocots, and other plant species are marked in red, blue and black, respectively. Branch color corresponds to that in Figure 1.
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Figure 7. Phylogeny of LBD proteins from Class IE in 18 species. This phylogeny was reconstructed using Class IE LBD proteins identified in Figure 1 and according to the same method described in Figure 1 legend. “*” means functionally characterized LBD protein in Table 2 (Gene ID is in brackets for LBD proteins of 18 species, species name is in square brackets for LBD proteins of other species). LBD proteins of eudicots, monocots, and other plant species are marked in red, blue and black, respectively. Branch color corresponds to that in Figure 1.
Figure 7. Phylogeny of LBD proteins from Class IE in 18 species. This phylogeny was reconstructed using Class IE LBD proteins identified in Figure 1 and according to the same method described in Figure 1 legend. “*” means functionally characterized LBD protein in Table 2 (Gene ID is in brackets for LBD proteins of 18 species, species name is in square brackets for LBD proteins of other species). LBD proteins of eudicots, monocots, and other plant species are marked in red, blue and black, respectively. Branch color corresponds to that in Figure 1.
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Figure 8. Phylogeny of LBD proteins from Class II in 18 species. This phylogeny was reconstructed using Class II LBD proteins identified in Figure 1 and according to the same method described in Figure 1 legend. “*” means functionally characterized LBD protein in Table 2 (Gene ID is in brackets for LBD proteins of 18 species, species name is in square brackets for LBD proteins of other species). LBD proteins of eudicots, monocots, and other plant species are marked in red, blue and black, respectively. Branch color corresponds to that in Figure 1.
Figure 8. Phylogeny of LBD proteins from Class II in 18 species. This phylogeny was reconstructed using Class II LBD proteins identified in Figure 1 and according to the same method described in Figure 1 legend. “*” means functionally characterized LBD protein in Table 2 (Gene ID is in brackets for LBD proteins of 18 species, species name is in square brackets for LBD proteins of other species). LBD proteins of eudicots, monocots, and other plant species are marked in red, blue and black, respectively. Branch color corresponds to that in Figure 1.
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Table
Table 1. Information on the 18 plant species for Lateral organ boundaries (LOB) domain (LBD) family analyses.
Table 1. Information on the 18 plant species for Lateral organ boundaries (LOB) domain (LBD) family analyses.
General ClassificationSpeciesGene Numbers in LBD FamilyData SourceGene ID Prefix
Green algaCylindrocystis brebissonii6China National GeneBank DatabaseRPGL/YOXI
MossPhyscomitrella patens30Gramene DatabasePp
FernSelaginella moellendorffii24Gramene DatabaseSELMO
Basal angiospermAmborella trichopoda20Gramene DatabaseAMTR
EudicotsArabidopsis thaliana43Gramene DatabaseAT
Beta vulgaris23Gramene DatabaseBVRB
Brassica napus118Gramene DatabaseBna
Daucus carota54Gramene DatabaseDCAR
Glycine max79Gramene DatabaseGLYMA
Gossypium raimondii65Gramene DatabaseB456
Medicago truncatula57Gramene DatabaseMTR
Solanum tuberosum39Gramene DatabasePGSC
MonocotsHordeum vulgare28Gramene DatabaseHORVU
Oryza sativa37Gramene DatabaseBGIOSGA
Setaria italica32Gramene DatabaseSETIT
Sorghum bicolor33Gramene DatabaseSORBI
Triticum aestivum86Gramene DatabaseTraesCS
Zea mays49Gramene DatabaseZm00001d
Table
Table 2. Functionally characterized LBD genes and their phylogenetic classification. “-” means “no reports so far”.
Table 2. Functionally characterized LBD genes and their phylogenetic classification. “-” means “no reports so far”.
ClassesSpeciesGenesBiological ProcessesTarget or Downstream GenesReferences
Class IAArabidopsisAtLBD25/
DDA1		Auxin signaling, photomorphogenesis-
(no reports so far)		[15]
ArabidopsisAtLOB/
ASL4		Leaf adaxial–abaxial polarity, floral organ development, brassinasteroid accumulationBAS1[2,59,60,61]
ArabidopsisAtLBD6/AS2Leaf adaxial–abaxial polarity,
floral organ development		BP, KNAT2[62,63,64,65,66]
ArabidopsisAtLBD36/AS1
ArabidopsisAtLBD10Pollen development-[67,68,69]
ArabidopsisAtLBD28Leaf adaxial–abaxial polarity, SAM genesis-[47]
RiceOsLBD1-9/
OsAS2;
OsIG1		Shoot differentiation, leaf development-[70]
Empty-glume identity, floral organ number control, female gametophyte developmentEG1, OsMADS1 and OsMADS6[71]
RiceOsRAMOSA2/
OsRA2		Panicle architecture establishmentLAX1, RCN2[54]
Maizeramosa2/
ra2		Inflorescence architecture establishment-[56]
MaizeIG1Embryo sac, leaf and tassel developmentKN1, RS1, LG3, LG4A/B, and KNOX3[57]
WheatTaAS2Leaf adaxial–abaxial polarity-[72]
BarleyVrs4/
HvRA2		Control lateral spikelet fertility and row-type pathwayVrs1, HvSRA and T6P[50]
AppleMdLBD11Leaf and flower development-[28]
Lotus japonicusLjLOB1Compound leaf development,
Floral development		-[46]
LjLOB3
Lotus japonicusSLPPulvinus development,
leaf movement		-[16]
MedicagoELP1/
PLP		Pulvinus development,
leaf movement		-[16,17,18]
PeaAPUPulvinus development,
leaf movement		-[16]
Class IBArabidopsisAtLBD14ABA-mediated lateral roots formationAtHB7 and AtHB12[51,73]
ArabidopsisAtLBD16Lateral roots formation, callus formation, gall formationFAD-BD, ARF7 and ARF19[21,40,43,44,52,74]
ArabidopsisAtLBD17Auxin-induced callus formation-[52,74]
ArabidopsisAtLBD18Tracheary element differentiation, lateral roots formation, callus formation, auxin signalingARF7 and ARF19, EXP14, E2Fa, VND6 and VND7[44,74,75,76]
ArabidopsisAtLBD19Callus formation-[77]
ArabidopsisAtLBD20Fusarium wilt susceptibility, jasmonate signalingMYC2, Thi2.1, VSP2, and PDF1.2[19]
ArabidopsisAtLBD29Lateral roots formation, callus formation, auxin signalingARF7 and ARF19[40,52,74,78]
ArabidopsisAtLBD30/
JLO		Tracheary element differentiation, embryogenesis, shoot, root and floral meristems development, auxin signalingVND6 and VND7[66,76,79,80]
ArabidopsisAtLBD33Auxin-mediated lateral roots formationARF7 and ARF19, E2Fa[75]
RiceOsDH1Floral organ development-[81]
RiceCrownrootless1
(crl1);
OsARL1		Auxin-mediated crown root formationFSM, GTE4 and MAP[42,82,83]
Auxin-mediated adventitious root formation-[84]
MaizeZmLBD2/
RTCS		Embryonic seminal and post-embryonic shoot-borne root initiation, auxin signalingZmArf34[5,41,85]
MaizeZmLBD43/
RTCL
Lotus japonicusLjLOB4Compound leaf development,
Floral development		-[46]
Class ICArabidopsisAtLBD3/
ASL9		Cytokinin-responsive biological events-[23]
ArabidopsisAtLBD12Growth of abaxial leaf surface, apical dominance and fertility-[86]
ArabidopsisAtLBD13Lateral root formation-[49]
ArabidopsisAtLBD15Tracheary element development, SAM developmentWUS[48,87]
RiceOsLBD3-7Leaf rolling-[55]
RiceOsLBD12-1SAM size controlAGO10[53]
Eucalyptus grandisEgLBD29Secondary xylem formation, response to Gibberellin (GA) and indol-3-acetic acid (IAA)-[35]
Eucalyptus grandisEgLBD37Secondary phloem formation, response to GA and IAA-[35]
CitrusCsLOB1Citrus bacterial canker disease susceptibility-[20]
Class IEArabidopsisAtLBD27Pollen development-[67,68,69]
Class IIArabidopsisAtLBD40GA response-[22]
ArabidopsisAtLBD41/
ASL38		Leaf adaxial-abaxial polarity-[88]
ArabidopsisAtLBD37Anthocyanin synthesis,
nitrogen responses		PAP1 and PAP2[24]
ArabidopsisAtLBD38
ArabidopsisAtLBD39
RiceOsLBD37Nitrogen metabolism, heading dateEhd1[25,26]
RiceOsLBD38Heading dateEhd1[26]
MedicagoMtLBD1Lateral roots emergence, auxin signalingHB1[58]

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MDPI and ACS Style

Zhang, Y.; Li, Z.; Ma, B.; Hou, Q.; Wan, X. Phylogeny and Functions of LOB Domain Proteins in Plants. Int. J. Mol. Sci. 2020, 21, 2278. https://doi.org/10.3390/ijms21072278

AMA Style

Zhang Y, Li Z, Ma B, Hou Q, Wan X. Phylogeny and Functions of LOB Domain Proteins in Plants. International Journal of Molecular Sciences. 2020; 21(7):2278. https://doi.org/10.3390/ijms21072278

Chicago/Turabian Style

Zhang, Yuwen, Ziwen Li, Biao Ma, Quancan Hou, and Xiangyuan Wan. 2020. "Phylogeny and Functions of LOB Domain Proteins in Plants" International Journal of Molecular Sciences 21, no. 7: 2278. https://doi.org/10.3390/ijms21072278

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