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Article

Genome-Wide Analysis and Abiotic Stress-Responsive Patterns of COBRA-like Gene Family in Liriodendron chinense

by
Chen Qiu
1,
Jinhui Chen
1,
Weihuang Wu
1,
Bojun Liao
1,
Xueyan Zheng
2,
Yong Li
2,
Jing Huang
3,
Jisen Shi
1,4,* and
Zhaodong Hao
1,4,*
1
State Key Laboratory of Tree Genetics and Breeding, Co-Innovation Center for Sustainable Forestry in Southern China, Nanjing Forestry University, Nanjing 210037, China
2
National Germplasm Bank of Chinese Fir at Fujian Yangkou Forest Farm, Nanping 353211, China
3
Jinling Institute of Technology, Nanjing 211169, China
4
Key Laboratory of Forest Genetics and Biotechnology of Ministry of Education, Nanjing Forestry University, Nanjing 210037, China
*
Authors to whom correspondence should be addressed.
Plants 2023, 12(8), 1616; https://doi.org/10.3390/plants12081616
Submission received: 7 March 2023 / Revised: 4 April 2023 / Accepted: 6 April 2023 / Published: 11 April 2023
(This article belongs to the Special Issue Plant Science Research in Nanjing Agricultural University: Commemorating the University’s 120th Anniversary)
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Abstract

:
The COBRA gene encodes a plant-specific glycosylphosphatidylinositol (GPI)-anchored protein (GAP), which plays an important role in cell wall cellulose deposition. In this study, a total of 7 COBRA-like (COBL) genes were identified in the genome of the rare and endangered woody plant Liriodendron chinense (L. chinense). Phylogenetic analysis showed that these LcCOBL genes can be divided into two subfamilies, i.e., SF I and II. In the conserved motif analysis of two subfamilies, SF I contained 10 predicted motifs, while SF II contained 4–6 motifs. The tissue-specific expression patterns showed that LcCOBL5 was highly expressed in the phloem and xylem, indicating its potential role in cellulose biosynthesis. In addition, the cis-element analysis and abiotic stress transcriptomes showed that three LcCOBLs, LcCOBL3, LcCOBL4 and LcCOBL5, transcriptionally responded to abiotic stresses, including cold, drought and heat stress. In particular, the quantitative reverse-transcription PCR (qRT-PCR) analysis further confirmed that the LcCOBL3 gene was significantly upregulated in response to cold stress and peaked at 24–48 h, hinting at its potential role in the mechanism of cold resistance in L. chinense. Moreover, GFP-fused LcCOBL2, LcCOBL4 and LcCOBL5 were found to be localized in the cytomembrane. In summary, we expect these results to be beneficial for research on both the functions of LcCOBL genes and resistance breeding in L. chinense.

1. Introduction

Cell walls play a vital role in protecting plants against biotic and abiotic stresses, as well as in plant support and protection [1,2,3]. The primary cell wall, consisting mainly of cellulose, hemicellulose, pectin and proteins, surrounds each plant cell. The secondary cell wall consists mainly of cellulose, hemicellulose and lignin, and, in specific cell types, is deposited between the plasma membrane and the primary cell wall after cell enlargement stops [4]. Cellulose, which is the most abundant biopolymer on Earth, is accumulated in plant cell walls [5]. Cellulose is a linear homopolysaccharide that makes up long and rigid microfibrils and is the load-bearing structure in cell walls [6]. The organization of cellulose is critical for directed plant growth [7,8]. The biosynthesis of cellulose is mediated by cellulose synthase (CesAs), which forms a rosette-like cellulose synthase complex (CSC) on the plasma membrane [5]. A genome-wide association study (GWAS) for culm cellulose content in barley (Hordeum vulgare) identified HvCOBRA, associated with cellulose synthesis [9]. The factors involved in cellulose synthesis were identified by Affymetrix microarray analysis in Arabidopsis thaliana, which indicated that COBRA homologous gene COBL4 was among the top 10 genes co-expressed with CESA4, 7 and 8, indicating a potential role of COBRA gene in protocell wall cellulose deposition [10].
COBRA is an important glycosylphosphatidylinositol (GP-I) anchor protein (GAP) that is mainly distributed along the longitudinal sides of the rapid elongation region of root cells and is involved in cellulose deposition to regulate cell expansion [11]. The COBRA protein contains four conserved domains: the N-terminal protein-targeting domain, the carbohydrate-binding motif domain, the conserved CCVS domain and the hydrophobic C-terminal domain [12]. Both the N-terminal domain and the hydrophobic C-terminal domain are cleaved after being translated [13]. The protein contains a GPI-anchored ω site in its C-terminal signal peptide, and the ω residue is cleaved and then attached to the C-terminus of the protein [14]. The N-terminal CBM domain preferentially interacts with crystalline cellulose. The C-terminus is where part of the GPI is located, and GPI anchoring is a post-translational modification that promotes the transport of certain proteins to the cell wall [15]. The CCVS domain is the third conserved domain in COB and is thought to be involved in disulfide bond formation or metal ion binding [16].
At present, COBL gene family members have been identified in A. thaliana (12) [14], Populus trichocarpa (18) [17], Oryza sativa (10) [18], Zea mays (9) [19], Pyrus bretschneideri (16) [20] and other plants. Initially, the COBL family was identified in Arabidopsis, having been isolated in a screening of Arabidopsis seedlings with abnormally extended roots [21]. Subsequently, functional studies were carried out in O. sativa [14], Zea mays [22], Triticum aestivum [23] and other monocotyledon plants. The results showed that COBL genes regulate the growth and development of plants. In Sorghum bicolor, an SbBC1 single-nucleotide mutation resulted in a decrease in mechanical strength, a decrease in cellulose content and an increase in lignin content. SbBC1 may mediate the mechanisms of cellulose biosynthesis and cell wall remodeling [24]. In wheat, the TaCOBL gene regulates seed coat and seed development by participating in the cellulose biosynthetic process of the plant cell wall and seed coat development [23]. In tomatoes, the SlCOBRA-like gene plays an important role in the epidermal cell walls of the fruits, increasing the hardness of the fruits and extending their shelf life [25]. COBLs also play important roles in adapting to stress. Genes related to drought, salinity and jasmonic acid (JA) stress were found in wheat [23], upland rice [26], Saccharum spontaneum [27] and Arabidopsis [28].
L. chinense belongs to the magnolia family, an ancient relict plant that plays an important role in evolution [29]. Currently, there are only two species in this genus, namely, L. chinense and Liriodendron tulipifera [30]. Liriodendron hybrids is a hybrid of L. chinense and L. tulipifera, with hybrid advantages that make it superior to its parent species in terms of flower color, timber properties and growth amount, and it is an important ornamental and economic tree species in China [31]. The genome sequencing and analysis of L. chinense showed that Magnoliaceae appeared before the differentiation of eudicots and monocots, which provided new ideas on the evolutionary status of Magnoliaceae and important support for the study of the molecular mechanisms related to L. chinense [30].
Based on previous reports, the COBL gene is involved in the cell wall biosynthesis of plant roots, stems, leaves and other mechanical tissues and plays a role in root development and adaptation to environmental stresses. Therefore, understanding the biological function of the COBL gene is of great significance for studying the mechanical strength and stress of plant stems. Currently, no studies on the identification of the COBL genes in Liriodendron have been reported. In this study, the genome data of L. chinense were analyzed to identify the members of the COBL gene family at the whole-genome level, and the evolutionary relationships, conserved motifs and chromosomal localizations of the members of the COBL gene family were analyzed using bioinformatics. The transcriptome data in different organs and under cold, heat and drought stress were analyzed to identify the gene expression pattern of COBL family members. Finally, quantitative reverse-transcription PCR (qRT-PCR) analysis further confirmed the expression levels of LcCOBL genes in multiple organs and under cold abiotic stresses. A subcellular localization experiment was conducted to verify the expression location of LcCOBL proteins. These results will provide a valuable foundation for further functional studies of LcCOBL genes in cellulose biosynthesis and under abiotic stresses.

2. Results

2.1. Identification of the COBL Gene Family in the L. chinense Genome

Seven COBL proteins were identified in L. chinense with BLAST using Arabidopsis COBL amino acid sequences as reference. They were submitted online to the NCBI-CDD website for conserved domain verification, and, finally, seven L. chinense COBL proteins were identified. According to their positions on the chromosome, they were named LcCOBL 1–7. The lengths of the 7 reported LcCOBL proteins to range from 230 to 655 aa, and their molecular weights range from 25.30 to 73.66 kDa (Table 1). The hydrophilicity values of all the LcCOBL proteins are less than 0 (Table 1), indicating that they are hydrophilic proteins (Figure S1). However, LcCOBL2, 4 and 5 in the LcCOBL family lack a GPI modification site (Figure S2). The signal peptide prediction results of LcCOBL proteins showed that all LcCOBL proteins had N-terminal signaling peptides (Figure S3). TMHMM results showed that only LcCOBL2 had 1 transmembrane domain (Figure S4). The subcellular localization predictions showed that all the LcCOBLs were located on the cell membrane, while LcCOBL2 may also play a role in chloroplasts (Table 1).

2.2. Phylogenetic Analysis of LcCOBL Proteins

In order to explore the phylogenetic relationships between the COBL proteins, we constructed a phylogenetic tree using 7, 12, 11, 11 and 8 COBL proteins from L. chinense, A. thaliana, O. sativa, Vitis vinifera and Amborella trichopoda, respectively (Figure 1). The results showed that seven LcCOBLs could be divided into two subfamilies, i.e., SF I and SF II, based on the phylogenetic tree (Figure 1). Four LcCOBLs were grouped in SF I, including LcCOBL1, LcCOBL2, LcCOBL4 and LcCOBL5, while the remaining three LcCOBLs were grouped in SF II. As for A. thaliana, O. sativa, V. vinifera and A. trichopoda, SF I contained seven, eight, seven and six family members, while SF II contained five, three, four and two family members, respectively. The phylogenetic grouping of the LcCOBL proteins was further confirmed with a phylogenetic tree constructed using only LcCOBL proteins (Figure S2).

2.3. Analyses of Locations, Structures and Conserved Motifs of LcCOBL Genes

In order to study the structural characteristics of the LcCOBL genes, we analyzed the conserved motifs and the exon–intron structures of the seven LcCOBL genes (Figure 2). Among these 10 motifs, only motifs 1 and 3 were possessed by all the LcCOBL proteins. Additionally, motif 4 contained a CCVS-conserved motif of the COBRA protein (Figure S3). The motif differences between the subfamilies were greater than those within the same subfamily, suggesting functional conservation among LcCOBL proteins within the same subfamily (Figure 2a,b). The LcCOBL genes contained 2–7 exons, and most of the evolutionarily related exon–introns shared similar structures (Figure 2c). In addition, the analysis of the conserved domains of the LcCOBLs showed that all the LcCOBLs possessed a COBRA domain or a COBRA superfamily domain (Figure 2c). These results further validate the reliability of the identified LcCOBL gene family and shed light on its functional evolution. The chromosomal distributions of the LcCOBL genes were determined based on the genome-wide data of L. chinense. The chromosomal localization analysis showed that seven LcCOBL genes were uniformly located on six chromosomes and one contig of L. chinense (Figure 3). There was only one gene on each chromosome with no tandem gene replication event.

2.4. Cis-Element Analysis of LcCOBL Promoters

Cis-elements distributed on gene promoters provide targets that bind to transcription factors, whereby gene expression patterns are activated or inhibited in the processes of plant growth and development and coping with external environmental stresses. We predicted the promoter cis-acting elements through the PlantCARE, which is based on probabilistic sequence models (e.g., Gibbs Sampling) [32]. Based on the conservation of the promoter sequences [33], motifs that have been determined in other species were selected from the screened elements for possible functional analysis in L. chinense. We found four major types of cis-acting elements i.e., related to light, hormones, environmental stress or developmental responsiveness, distributed on the promoter regions of the LcCOBLs (Figure 4). Among the light-response-related cis-elements, G-box was the most abundant type, which can be found within all LcCOBL promoters. Regarding hormones and environmental stress, we found that the ABA- (ABRE) and drought-related (MYC and as-1) cis-elements were the most abundant cis-elements, showing that LcCOBLs might play an important role in the response to drought stress. As for the development-related cis-elements, we found that the most abundant type has a function in meristem expression.

2.5. Organspecific Expression Patterns of LcCOBLs

To further explore the potential functions of the LcCOBL family in tissue development, we investigated the expression patterns of the LcCOBLs across different organs of L. chinense (Figure 5a). According to the transcriptome data regarding eight tissues, namely bark, bud, phloem, sepal, stamen, stigma and xylem. We found that five LcCOBL genes were expressed in these selected organs, except for two genes (LcCOBL6 and LcCOBL7). Moreover, these five LcCOBL genes were mainly expressed in the phloem, stamen, stigma and xylem tissues, with almost no expression in the bark, bud or sepal tissues. Interestingly, LcCOBL5 was mainly expressed in the phloem and xylem tissues, showing its potential role in stem growth. Furthermore, a quantitative reverse-transcription PCR (qRT-PCR) analysis confirmed the higher expression of LcCOBL5 in the stems than in the roots and leaves (Figure 5b).

2.6. Expression Patterns of LcCOBLs in Response to Abiotic Stresses

To analyze the responses of the LcCOBL genes to abiotic stresses, we examined the expression levels of these LcCOBLs under cold, drought and heat stress based on the available RNA-seq data (Figure 6a–c). The results show that three LcCOBLs, i.e., LcCOBL3, LcCOBL4 and LcCOBL5, transcriptionally responded to these abiotic stresses. Specifically, LcCOBL3 was highly up-regulated in response to these abiotic stresses and peaked at 12–24 h, 1 d and 3 d under cold, drought and heat stress, respectively. In contrast, LcCOBL5 was dramatically down-regulated as soon as it was exposed to these stresses. Compared with LcCOBL5 and LcCOBL3, the expression dynamic of LcCOBL4 was less violent, although it first increased and then decreased.
To further determine whether the expression levels of the LcCOBL genes were influenced by abiotic stresses, Liriodendron seedlings treated with low-temperature conditions (4 °C) were collected to quantify the expression levels of the LcCOBLs using qRT-PCR analysis. The results show that each gene has a different expression pattern after cold treatment (Figure 6d). The expression level of LcCOBL3 in the experimental group was significantly increased compared with the control group, while the expression level of LcCOBL2 in the treatment group was decreased. LcCOBL4 and LcCOBL5 showed opposing expression patterns. LcCOBL4 expression was downregulated at 6 h and then upregulated. LcCOBL5 was upregulated at 24 h and then downregulated. This suggests that the LcCOBLs exhibit different expression trends under stress treatment, indicating that these genes respond to the regulation of abiotic stress to varying degrees.

2.7. Subcellular Localization of LcCOBL Proteins

To further explore the potential roles of these LcCOBL proteins, we cloned the full-length CDSs of three LcCOBLs, i.e., LcCOBL2, LcCOBL4 and LcCOBL5 (Supplementary Table S2). Then, these LcCOBL genes without terminating codons were inserted into pJIT166 vectors to obtain LcCOBL-GFP fusion vectors, which were driven by a 35S promoter. Then, these three vectors were separately transferred into the protoplasts of L. chinense calli via PEG-mediated protoplast transformation and transferred into onion epidermal cells by gene gun. At the same time, the 35S:H2B-mCherry vector was transferred into callus protoplasts as the control for the nuclear localization. The results show that the protoplasts transferred with the 35S:GFP vector expressed the GFP signal in the whole cell, which was a constitutive expression, while in 35S:H2B-mCherry lines, the mCherry signal was only observed in the nucleus. Furthermore, for the LcCOBL5-GFP fusion vectors, the GFP signal was found in the cytomembrane, and the weak fluorescence signal was also observed in the cytoplasm (Figure 7). However, we cannot determine the expression of LcCOBL2, 4 proteins in other organelles except cytomembrane (Figure S7). This requires further experiments to verify.

3. Discussion

3.1. Functions of LcCOBLs in Stem Development and Stress Responses

In phylogenetic trees, genes with similar clusters may have similar functions. Therefore, LcCOBLs are likely to have similar biological functions to COBL proteins known to be in other species in this group. It was stated that genes with less intron number may be expressed faster than other genes by upstream signals [34]. Combining the gene expression patterns of members of the COBL gene families helps to predict the gene functions of the LcCOBL gene family members. At present, many genes related to brittle traits, including OsBCIL4 and OsBC1, that have been resolved have been reported in rice, indicating that the bc mutant gene in rice controls the culm mechanical strength mainly by influencing cellulose metabolic enzymes [14,35]. A phylogenetic analysis showed that LcCOBL1 and LcCOBL3 are homologous with OsBC1Lp1, OsBC1L1 and OsBC1L8 in rice, respectively, and may be involved in the metabolic synthesis of cellulose. Studies on Atcob-1 have shown that AtCOB is an important factor in the highly anisotropic expansion of plant morphogenesis by participating in the directional growth of cellulose microfibrils [36]. LcCOBL4 has high homology with AtCOB and may be involved in the directional expansion of cellulose microfibrils.
The expression patterns of the LcCOBLs in different tissues showed that all LcCOBLs except LcCOBL1 were highly expressed in stems, followed by roots. In the root, stem and leaf tissues of the plant, the cellulose contents in the stems, roots and leaves ranged from the highest to lowest, respectively, which further proves that LcCOBLs are associated with cellulose biosynthesis. In Arabidopsis, COBL proteins are key regulators of the direction of cell expansion in roots. In the identification of the expression sequence markers of potential homologous genes in other plants, it has been shown that COBL-gene-related functions may be necessary for all vascular plants [16]. The content of cellulose in the root tips of Arabidopsis mutants was significantly reduced, and the root cells were laterally expanded, suggesting that the regulation of cell directional expansion by COB is related to cellulose deposition [11]. In rapeseed (Brassica napus), RNA-seq analysis showed that BnaCOBL9, BnaCOBL35 and BnaCOBL41 were highly expressed in stems with high breaking resistance and may be involved in the stem development and stem-breaking resistance of rapeseed [37]. Combining these findings with those of previous studies, LcCOBL genes may be involved in plant cellulose synthesis and enhance stem fracture resistance.
To investigate the functions of the LcCOBLs in cold stress, we used qRT-PCR to analyze the expression patterns of the LcCOBLs in stems under low-temperature (4 °C) treatment. Over different processing times, different LcCOBLs showed different expression trends. Moreover, in the cis-elements analysis of LcCOBL promoters, each LcCOBL gene had elements related to low temperature. These results suggest that these LcCOBL genes may help improve the cold tolerance of plants. Similarly, previous studies have shown that COBL genes play important roles in drought and salt tolerance in other species [19,26,27].

3.2. Subcellular Localization of LcCOBLs and Their Associations with Potential Functions

Plant extracellular pH is acidic (pH 5.7), and many physiological and external environmental factors can cause changes in extracellular pH [38]. It was found that GFP was pH sensitive and its fluorescence decreased significantly under acidic conditions [39]. Although the shape of the spectrum does not change significantly with pH, the intensity gradually decreases with lowered pH, decreasing to 50% of maximal intensity at a pH of ~6 [40,41]. TMHMM results showed that only LcCOBL2 had 1 transmembrane domain. However, a glycosylphosphatidylinositol (GPI) anchor is an alternative means of attaching a protein to the membrane [42]. As LcCOBL proteins are anchored to the outer layer of the cytoplasmic membrane and in an acidic environment, the GFP signal is weakened, resulting in an unclear fluorescence signal in the result images. The current experimental results show that, for the LcCOBL5-GFP fusion vector, the GFP signal was found in the cytomembrane, the weak fluorescence signal was also observed in the cytoplasm (Figure 7). However, we cannot determine the expression of LcCOBL2, 4 proteins in other organelles except cytomembrane (Figure S7). This requires further experiments to verify.
The result of subcellular localization indicated that the LcCOBL5 in L. chinense calli and onion epidermal cells are localized in the cytomembrane and cytoplasm, which is consistent with the results of other species. By imaging living cells in Arabidopsis, it was found that COBL was located in particles in the plasma membrane [1,43]. In onion epidermal cells bombarded with an Ubi::OsBC1L4:GFP vector, GFP signals were found in the cell wall and plasma membrane [35]. This is consistent with the results of COB being observed in the elongation region of Arabidopsis roots using transmission electron microscopy. COB exists in the plasma membrane and some cell walls [36]. However, in Cunninghamia lanceolata, the fused ClCOBL1-RFP protein is transformed into tobacco cells. RFP signals mainly exist in the cell wall and membrane, but there is also a weak signal in the cytoplasm [43]. The COBRA gene encodes a plant-specific glycosylphosphatidylinositol (GPI)-anchored protein (GAP). GPI biosynthesis and transfer to proteins are carried out on the endoplasmic reticulum [13,44]. It may be that the process of GPI biosynthesis and transfer leads to the detection of fluorescence signals in the cytoplasm. Based on the above analysis, there are differences in the expression positions of COBL genes in different species, but most of the members are mainly expressed in the plasma membrane, a few in the cytoplasm, indicating that LcCOBLs participate in a variety of biological regulation processes.

4. Materials and Methods

4.1. Identification of the LcCOBLs Family in the L. chinense Genome

L. chinense protein sequences were downloaded from (https://hardwoodgenomics.org/Genome-assembly/2630420) (accessed on 3 March 2022). Firstly, the protein sequences of each member of the Arabidopsis COBL gene family were downloaded from the Arabidopsis genome database (Phytozome) [45] (https://phytozome-next.jgi.doe.gov) (accessed on 3 March 2022). Based on a BLASTp search [46] (E-value ≤ 1 × 10−5), LcCOBL family members were identified. Second, the HMM file corresponding to the COBRA domain (PF04833) was downloaded from the Pfam protein family database [47,48] (https://www.ebi.ac.uk/interpro/) (accessed on 2 March 2022). The search in the L. chinense protein database was carried out via an HMM search, and the sequences containing this domain were screened, and duplicate sequences were removed. Then, the NCBI-CDD database (https://www.ncbi.nlm.nih.gov/Structure/cdd/wrpsb.cgi) (accessed on 3 March 2022) was used to analyze the encoding protein characteristics of the LcCOBLs to ensure that the LcCOBLs had COBRA domains. Finally, seven LcCOBL genes were identified in the L. chinense genome. Furthermore, the basic features of the LcCOBL proteins of L. chinense (sequence length; MW; pI) were identified using ExPasy (https://prosite.expasy.org) (accessed on 30 October 2022). TMHMM Server v. 2.0 (https://dtu.biolib.com/DeepTMHMM) (accessed on 30 October 2022) was used to predict the protein transmembrane domains. The N-terminal signal peptide prediction of LcCOBL proteins was carried out using SignalP-6.0 (https://services.healthtech.dtu.dk/services/SignalP-6.0/) (accessed on 3 March 2023). Target P (https://services.healthtech.dtu.dk/services/NetGPI-1.1/) (accessed on 3 March 2023) was used to analyze the anchor sites at the hydrophobic end of the C-terminal. Subcellular localization prediction was performed using Cell-PLoc 2.0 (http://www.csbio.sjtu.edu.cn/bioinf/Cell-PLoc-2/) (accessed on 30 October 2022).

4.2. Phylogenetic Analysis and Classification of the LcCOBL Family

According to the classification of the COBL proteins of Arabidopsis, 7 COBL proteins of L. chinense were divided into 2 groups. The COBL family protein sequences of A. thaliana, O. sativa, V. vinifera and A. trichopoda were downloaded from the Phytozome database (https://phytozome-next.jgi.doe.gov/) (accessed on 28 March 2022). The full-length COBL protein sequences were aligned using the clustalx tool. TrimAl (‘automated1’ mode) was used to trim the aligned sequences to generate the trimmed MSA file, which was then used to build the COBL phylogenetic tree. Using BEAUti software, the clipped FASTA file was output into an XML format. After the BEAUti program was completed, the TreeAnnotator program was used to construct the Bayesian phylogenetic tree. The TreeAnnotator program set the posterior probability limit to 1.0, the Burnin percentage to 90, the target tree type to maximum branch confidence tree, and the node height to common ancestor heights. Finally, the tree was visualized with the online iToL (https://itol.embl.de/) (accessed on 1 March 2023).

4.3. Analyses of the Chromosomal Locations, Structures and Conserved Motifs of LcCOBL Genes

The phylogenetic relationships between the LcCOBL genes were analyzed with MEGA X using the maximum likelihood (ML) method with 1000 bootstrap replicates. The position information of the LcCOBL genes on the chromosome was picked up from the L. chinense annotations using TBtools [49]. MEME (https://meme-suite.org/meme/doc/meme.html) (accessed on 31 March 2022) was further carried out to investigate their conserved motifs [50]. The GFF annotation files and the conserved structure sequences were imported into TBtools to visualize the exon–intron structures and COBRA domains. The GFF annotated files were obtained from the L. chinense genome file, and the conservative structural sequences were obtained from the NCBI (https://www.ncbi.nlm.nih.gov/Structure/cdd/wrpsb.cgi) (accessed on 30 October 2022). In addition, the software PlantCARE (https://bioinformatics.psb.ugent.be/webtools/plantcare/html/) (accessed on 7 April 2022) was used to predict the cis-acting elements of the 7 LcCOBL genes in the upstream 2000 bp range.

4.4. Plant Materials, RNA Extraction, qRT-PCR Analysis, and Transcriptome Sequencing Analysis of Abiotic Stress in L. chinense

The Liriodendron hybrids plants used in this study were obtained from the Key Laboratory of Forest Genetics and Biotechnology of the Ministry of Education at Nanjing Forestry University. Liriodendron hybrids seedlings generated via somatic embryogenesis were cultured in a greenhouse under light 16 h/dark 8 h conditions (temperature, 25 °C; humidity, 70%).
In the tissue-specific expression experiments, leaf, root and stem tissues were taken from 3-month-old tissue culture bottle seedlings. Under abiotic stress, 3-month-old tissue culture bottle seedlings were cultured in a cold (4 °C) growth chamber. Stem tissues from the treatment group and control group were collected at 0, 6, 24 and 48 h after the experiment and stored at −80 °C.
Total RNA was isolated from each sample using the Eastep®Super Total RNA Extraction Kit (Promega), and first-strand cDNA was synthesized from the proposed RNA using a PrimeScript RT Master Mix (Takare). A qPCR SYBR Green Master Mix (Vazyme) was used for real-time quantitative PCR, and the GAPDH gene was used as the internal control gene [51]. The real-time PCR cycling parameters were 95 °C for 30 s, followed by 45 cycles at 95 °C for 5 s and 60 °C for 30 s, with a melting curve analysis. All reactions were performed in triplicate to ensure the repeatability of the results. Gene expression levels were calculated using 2−∆∆Ct.
The seedlings generated through somatic embryogenesis grown at 22 °C, light 16 h/dark 8 h, 75% relative humidity were treated at 4 °C, 40 °C or 15% PEG 6000 for 1 h, 3 h, 6 h, 12 h, 1 day and 3 days, respectively, and were treated with cold, heat and drought. Each treatment consisted of five replicates for each sampling time, taking leaf tissue samples for RNA-seq analysis. The transcriptome data about cold and heat stress (PRJNA679089) and drought stress (PRJNA679101) could be downloaded from NCBI [52]. The transcriptome data are in regards to eight organs from the author of this paper [30].

4.5. Subcellular Localization

In order to verify the prediction results of the subcellular localization of the LcCOBL proteins, we cloned the full-length CDSs of three LcCOBLs, i.e., LcCOBL2, LcCOBL4 and LcCOBL5. Then, these LcCOBL genes without terminating codons were inserted into pJIT166 vectors to obtain LcCOBL-GFP fusion vectors, which were driven by a 35S promoter. Then, these three vectors were separately transferred into the protoplasts of L. chinense calli via PEG-mediated protoplast transformation and transferred into onion epidermal cells by gene gun. At the same time, the 35S:H2B-mCherry vector was transferred into callus protoplasts as the control for the nuclear localization. The plasmids of the corresponding vectors were extracted, and the final concentration reached 1 ug/uL for use. Appropriate amounts of calli were put into the culture dishes, and an enzymatic solution was added to separate the cell walls from the protoplasts. They were then placed in a shaker at 27 °C at 40 rpm and enzymolyzed in the dark for 3–6 h. The carrier plasmid was added to the isolated and purified protoplast solutions, and a PEG solution of equal volume was added. The vectors were transferred into protoplasts via PEG mediation. Finally, the positions of GFP and mCherry were observed and photographed with a confocal laser microscope.
In order to further verify the subcellular localization of LcCOBL proteins, onion epidermal cells were transformed with the 35S: LcCOBL2, 4 5-GFP vectors by gene gun, with 35S: GFP vector as a control. The bombarded cells were incubated in the dark at 22–24 °C for 12–24 h to allow transient expression of the proteins. The GFP location was observed and photographed with a fluorescent microscope.

5. Conclusions

In this study, a genome-wide analysis of the LcCOBL gene family was conducted by focusing on their genetic structures and responses to stress treatments, and a total of seven LcCOBL genes were identified. The chromosomal distributions, gene structures and motifs, cis-regulatory elements in the promoter region, and expression patterns of the LcCOBL genes under different stress treatments and subcellular localizations were analyzed. The subcellular localization analysis and experimental results show that the LcCOBL genes are localized in the cytoplasm. The tissue expression pattern analysis of the LcCOBL genes shows that the LCCOBL genes are highly expressed in plant stems and may be involved in cellulose biosynthesis. The LcCOBL genes showed different response trends under cold, heat and drought stress treatments, indicating that they play a role in coping with environmental stresses. These results provide basic information on the COBL gene family and a good platform for exploring the specific roles of these genes in stress tolerance and the development of L. chinense.

Supplementary Materials

The following supporting information can be downloaded at https://www.mdpi.com/article/10.3390/plants12081616/s1. Figure S1: Hydrophobicity analysis of amino acid sequences of LcCOBLs; Figure S2: Prediction results of GPI modification sites of protein sequences of LcCOBL; Figure S3: Prediction results of signal peptides of protein sequences of LcCOBL; Figure S4: Prediction results of transmembrane domains of LcCOBL proteins; Figure S5: ClustalW was used for multi-sequence alignment of LcCOBL protein sequences; Figure S6: Amino acid sequences of each motif; Figure S7: Subcellular localization of LcCOBL2, 4 proteins in L. chinense calli and in onion epidermal cells; Table S1: Protein names and sequences of COBL; Table S2: Primer sequences of LcCOBL proteins for subcellular localization; Table S3: Primer sequences of LcCOBLs and reference genes in qRT-PCR.

Author Contributions

Conceptualization, C.Q.; methodology, C.Q.; software, B.L.; validation, Z.H.; resources, X.Z.; formal analysis, Y.L.; methodology, J.H.; writing—original draft preparation, C.Q.; writing—review and editing, C.Q., W.W. and Z.H.; supervision, J.C.; project administration, J.C. and J.S. All authors have read and agreed to the published version of the manuscript.

Funding

This research was supported by the National Key R&D Program of China during the fourteenth five-year plan period (2021YFD2200103), the Youth Foundation of the Natural Science Foundation of Jiangsu Province (Grant No. BK20210614), and the Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD).

Data Availability Statement

The original contributions presented in this study are publicly available. The L. chinense protein sequences can be found at https://hardwoodgenomics.org/Genome-assembly/2630420 (accessed on 3 March 2022). The RNA sequences can be obtained from the NCBI, accession numbers PRJNA679089 and PRJNA679101.

Acknowledgments

We thank Nanjing Forestry University for providing a platform for our experiments.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. Phylogenetic tree of COBL protein family in L. chinense, A. thaliana, O. sativa, V. vinifera and A. trichopoda. The full-length COBL protein sequences were aligned using the clustalx tool, and the Bayesian method was used to construct the phylogenetic tree in BEAUti. Finally, the tree was visualized with the online iToL. The bootstrap values are supported by 1000 replications and are shown beside the branches. According to the phylogenetic tree, the seven LcCOBLs could be divided into two subfamilies (SF I and SF II), where SF I stands for LcCOBL subfamily I and SF II stands for LcCOBL subfamily II.
Figure 1. Phylogenetic tree of COBL protein family in L. chinense, A. thaliana, O. sativa, V. vinifera and A. trichopoda. The full-length COBL protein sequences were aligned using the clustalx tool, and the Bayesian method was used to construct the phylogenetic tree in BEAUti. Finally, the tree was visualized with the online iToL. The bootstrap values are supported by 1000 replications and are shown beside the branches. According to the phylogenetic tree, the seven LcCOBLs could be divided into two subfamilies (SF I and SF II), where SF I stands for LcCOBL subfamily I and SF II stands for LcCOBL subfamily II.
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Figure 2. Conserved motifs and structures of LcCOBL genes. (a) ClustalW was used for multi-sequence alignment of LcCOBL protein sequences. A maximum likelihood (ML) tree was built using MEGA X and 1000 bootstrap repeats. (b) The conserved motifs of LcCOBL proteins were revealed using MEME analysis. The colored box on the right represents 10 motifs. (c) The gene structures. Yellow boxes, black lines, green boxes, pink boxes and dark green boxes represent exons, introns, UTRs (untranslated regions), COBRA domains and COBRA superfamily domains, respectively.
Figure 2. Conserved motifs and structures of LcCOBL genes. (a) ClustalW was used for multi-sequence alignment of LcCOBL protein sequences. A maximum likelihood (ML) tree was built using MEGA X and 1000 bootstrap repeats. (b) The conserved motifs of LcCOBL proteins were revealed using MEME analysis. The colored box on the right represents 10 motifs. (c) The gene structures. Yellow boxes, black lines, green boxes, pink boxes and dark green boxes represent exons, introns, UTRs (untranslated regions), COBRA domains and COBRA superfamily domains, respectively.
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Figure 3. Chromosomal location analysis of LcCOBLs. The size of a chromosome is expressed by its relative length. Scale bar on the left indicates the chromosome lengths (Mb).
Figure 3. Chromosomal location analysis of LcCOBLs. The size of a chromosome is expressed by its relative length. Scale bar on the left indicates the chromosome lengths (Mb).
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Figure 4. Analysis of cis-elements on LcCOBL promoters. Cis-elements in the upstream 2000 bp area of LcCOBL promoters. Different colors in the table indicate different types of promoters, and numbers indicate the numbers of different promoter elements.
Figure 4. Analysis of cis-elements on LcCOBL promoters. Cis-elements in the upstream 2000 bp area of LcCOBL promoters. Different colors in the table indicate different types of promoters, and numbers indicate the numbers of different promoter elements.
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Figure 5. The expression patterns of LcCOBL genes in different L. chinense organs. (a). Expression profiles of LcCOBL genes in bark, bud, phloem, sepal, stamen, stigma and xylem tissues. The heatmap data were averaged and plotted using TBtools, with red representing a high expression level and blue representing a low expression level. (b) qRT-PCR analysis of LcCOBL genes in different organs including leaves, roots and stems. The expression levels of related genes were calculated with 2−ΔΔCt using a leaf as control. Mean values ± SE are shown for the 3 replicates, and the levels of significance relative to the control are ns: no significant difference, * p < 0.05 and ** p < 0.01.
Figure 5. The expression patterns of LcCOBL genes in different L. chinense organs. (a). Expression profiles of LcCOBL genes in bark, bud, phloem, sepal, stamen, stigma and xylem tissues. The heatmap data were averaged and plotted using TBtools, with red representing a high expression level and blue representing a low expression level. (b) qRT-PCR analysis of LcCOBL genes in different organs including leaves, roots and stems. The expression levels of related genes were calculated with 2−ΔΔCt using a leaf as control. Mean values ± SE are shown for the 3 replicates, and the levels of significance relative to the control are ns: no significant difference, * p < 0.05 and ** p < 0.01.
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Figure 6. The expression patterns of LcCOBL genes in L. chinense under abiotic stresses. (a–c) Expression profiles of LcCOBL genes in L. chinense under biotic stresses, including cold (a), drought (b) and heat (c) stress. The heatmap data were averaged and plotted using TBtools, with red representing a high expression level and blue representing a low expression level; (d) qRT-PCR analysis of LcCOBL genes under cold abiotic stress. The expression levels of related genes were calculated with 2−∆∆Ct using 0 h as control. Mean values ± SE are shown for the 3 replicates, and the levels of significance relative to the control are ns: no significant difference, *: 0.01 ≤ p < 0.05, **: 0.001 ≤ p < 0.01 and ***: p < 0.001.
Figure 6. The expression patterns of LcCOBL genes in L. chinense under abiotic stresses. (a–c) Expression profiles of LcCOBL genes in L. chinense under biotic stresses, including cold (a), drought (b) and heat (c) stress. The heatmap data were averaged and plotted using TBtools, with red representing a high expression level and blue representing a low expression level; (d) qRT-PCR analysis of LcCOBL genes under cold abiotic stress. The expression levels of related genes were calculated with 2−∆∆Ct using 0 h as control. Mean values ± SE are shown for the 3 replicates, and the levels of significance relative to the control are ns: no significant difference, *: 0.01 ≤ p < 0.05, **: 0.001 ≤ p < 0.01 and ***: p < 0.001.
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Figure 7. Subcellular localization of LcCOBL5 protein in L. chinense calli (a) and onion epidermal cells (b). In these pictures, GFP indicates green fluorescence photography, bright field indicates bright-field photography, RFP indicates red fluorescence photography and merged indicates the fusion of green fluorescence, red fluorescence and bright field photography. The red fluorescence locates the nucleus, and the green fluorescence locates the LcCOBL proteins.
Figure 7. Subcellular localization of LcCOBL5 protein in L. chinense calli (a) and onion epidermal cells (b). In these pictures, GFP indicates green fluorescence photography, bright field indicates bright-field photography, RFP indicates red fluorescence photography and merged indicates the fusion of green fluorescence, red fluorescence and bright field photography. The red fluorescence locates the nucleus, and the green fluorescence locates the LcCOBL proteins.
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Table
Table 1. List of gene IDs and characteristics of the LcCOBL genes.
Table 1. List of gene IDs and characteristics of the LcCOBL genes.
Gene NameGene IDLocusMW (kDa) apI bGRAVY cN-Terminal Signal PeptideGPI Modification SiteSubcellular Location
LcCOBL1Lchi01857Chr242.968.43−0.271YesYesCell membrane
LcCOBL2Lchi02570Chr559.668.81−0.245YesNoCell membrane; chloroplasts
LcCOBL3Lchi20746Chr1070.305.53−0.059YesYesCell membrane
LcCOBL4Lchi12311Chr1340.588.95−0.199YesNoCell membrane
LcCOBL5Lchi14677Chr1625.307.53−0.239YesNoCell membrane
LcCOBL6Lchi21892Chr1973.598.47−0.28YesYesCell membrane
LcCOBL7Lchi34460Contig298273.668.45−0.271YesYesCell membrane
a Molecular weight. b Isoectric point. c Grand average of hydropathy.
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Qiu, C.; Chen, J.; Wu, W.; Liao, B.; Zheng, X.; Li, Y.; Huang, J.; Shi, J.; Hao, Z. Genome-Wide Analysis and Abiotic Stress-Responsive Patterns of COBRA-like Gene Family in Liriodendron chinense. Plants 2023, 12, 1616. https://doi.org/10.3390/plants12081616

AMA Style

Qiu C, Chen J, Wu W, Liao B, Zheng X, Li Y, Huang J, Shi J, Hao Z. Genome-Wide Analysis and Abiotic Stress-Responsive Patterns of COBRA-like Gene Family in Liriodendron chinense. Plants. 2023; 12(8):1616. https://doi.org/10.3390/plants12081616

Chicago/Turabian Style

Qiu, Chen, Jinhui Chen, Weihuang Wu, Bojun Liao, Xueyan Zheng, Yong Li, Jing Huang, Jisen Shi, and Zhaodong Hao. 2023. "Genome-Wide Analysis and Abiotic Stress-Responsive Patterns of COBRA-like Gene Family in Liriodendron chinense" Plants 12, no. 8: 1616. https://doi.org/10.3390/plants12081616

APA Style

Qiu, C., Chen, J., Wu, W., Liao, B., Zheng, X., Li, Y., Huang, J., Shi, J., & Hao, Z. (2023). Genome-Wide Analysis and Abiotic Stress-Responsive Patterns of COBRA-like Gene Family in Liriodendron chinense. Plants, 12(8), 1616. https://doi.org/10.3390/plants12081616

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