- Research article
- Open Access
Characterization of bHLH/HLH genes that are involved in brassinosteroid (BR) signaling in fiber development of cotton (Gossypium hirsutum)
- Rui Lu†1,
- Jiao Zhang†1,
- Dong Liu1,
- Ying-Li Wei1,
- Yao Wang1 and
- Xue-Bao Li1Email authorView ORCID ID profile
© The Author(s). 2018
- Received: 14 August 2018
- Accepted: 14 November 2018
- Published: 27 November 2018
Basic helix-loop-helix/helix-loop-helix (bHLH/HLH) transcription factors play important roles in plant development. Many reports have suggested that bHLH/HLH proteins participate in brassinosteroid (BR) hormone signaling pathways to promote cell elongation. Cotton fibers are single-cells and derived from seed surface. To explore the roles of bHLH/HLH proteins in cotton fiber development progress by modulating BR signaling pathway, we performed a systematic analysis of the bHLH/HLH gene family in upland cotton (Gossypium hirsutum) genome.
In this study, we identified 437 bHLH/HLH genes in upland cotton (G. hirsutum) genome. Phylogenetic analysis revealed that GhbHLH/HLH proteins were split into twenty six clades in the tree. These GhbHLH/HLH genes are distributed unevenly in different chromosomes of cotton genome. Segmental duplication is the predominant gene duplication event and the major contributor for amplification of GhbHLH/HLH gene family. The GhbHLH/HLHs within the same group have conserved exon/intron pattern and their encoding proteins show conserved motif composition. Based on transcriptome data, we identified 77 GhbHLH/HLH candidates that are expressed at relatively high levels in cotton fibers. As adding exogenous BR (brassinolide, BL) or brassinazole (Brz, a BR biosynthesis inhibitor), expressions of these GhbHLH/HLH genes were up-regulated or down-regulated in cotton fibers. Furthermore, overexpression of GhbHLH282 (one of the BR-response genes) in Arabidopsis not only promoted the plant growth, but also changed plant response to BR signaling.
Collectively, these data suggested that these GhbHLH/HLH genes may participate in BR signaling transduction during cotton fiber development. Thus, our results may provide a valuable reference data as the basis for further studying the roles of these bHLH/HLH genes in cotton fiber development.
- Cotton (Gossypium hirsutum)
- bHLH/HLH transcription factor
- Fiber development
- Phylogenetic analysis
- Brassinosteroid (BR) signaling
- Gene expression
Cotton, one of the most important economic crops, supplies the largest number of natural fibers in the textile market around the world. The cotton genus (Gossypium) is composed of nearly 50 species, of which four species, including two diploids (G. arboreum and G. herbaceum, 2n = 2× = 26 AA) and two allotetraploids (G. hirsutum and G. barbadense, 2n = 4× = 52 AADD), have been widely cultivated for the commercial values of fibers . Upland cotton (G. hirsutum) accounts for the largest planting area among the varieties of cotton crops and provides most of the valuable fibers needed by modern textile industry. Fiber development is divided into four overlapping stages, fiber initiation, elongation, secondary cell wall thickening and maturity . The cotton fiber is regarded as a powerful cell research model since it is an easily isolated single cell with distinct stages of cotton fiber cell development. In vitro ovules culture can be carried out to make further research about detailed development stages of cotton fibers [3, 4].
Basic helix loop helix/helix loop helix (bHLH/HLH) proteins were named for the basic helix loop helix domains. The bHLH domains are comprised of 50–60 amino acids with two functionally different regions, the N terminal basic region and the C terminal helix-loop-helix region. The basic region, consisting of around 15 amino acids with numerous basic residues, can recognize and bind to DNA [5, 6]. The HLH region, including two amphipathic α-helices that are parted by a loop region with alterable sequence, can form the dimers with other HLH domains . In higher plants, the bHLH/HLH proteins participate in regulation of plant growth and development, such as light signal transmission, plant hormone signals and organs development. For example, in light signal transmission, AtPIF4 takes part in regulating photomorphogenesis mainly by interacting with photochromes . AtSPT is not only related to Arabidopsis sterility, but also has a coordinating relationship with DELLA protein to regulate the expression of gibberellins (GA) response genes jointly. AtSPT mutation can remove its inhibition of cell growth [9, 10]. AtGL3 is also involved in the development of Arabidopsis trichomes by contributing to form the trichome promoting comlpex TTG1/GL3 (EGL3) /GL1 [11, 12]. In the stem or leaf epidermal cells of Arabidopsis, the complex can induce the expression of the downstream gene GL2 to determine the development of epidermal cells. And the MYB proteins, AtCPC, AtTRY, AtTCL1 and AtETC1, can bind to GL3 competing with GL1, thereby negatively regulating the initiation of trichomes [13, 14].
Brassinosteroid (BR) signalling is a well-described signalling pathway in Arabidopsis that plays a crucial role in plant growth and development. Many bHLH/HLH protiens have been reported to be involved in the BR signaling transduction. AtbHLH064 (HBI1), AtbHLH158 (IBH1), AtbHLH044/058/050 (BEE1/2/3), AtbHLH046/102/141 (BIM1/2/3), AtbHLH136/135 (PRE1/3) and AtbHLH150/148/147/149 (AIF1/2/3/4) are regulated by BZR1/BES1 to influence BR signaling in Arabidopsis [15–19]. Most of them can form homodimers and heterodimers, endowing them with the capacity to function in the regulation of multiple transcriptional programs . For example, AtCESTA can form heterodimer with AtbHLH044 (BEE1) to regulate the expression of BR biosynthesis related gene CPD positively . AtbHLH064 (HBI1) promotes cell elongation by regulating downstream genes expression and its functions can be inhibited by AtbHLH158 (IBH1), which inhibition can be relieved by the interaction of AtbHLH136 (PRE1) and AtbHLH158 (IBH1) [22, 23]. A report also demonstrates that AtbHLH136 (PRE1), AtbHLH158 (IBH1) and AtbHLH049/074/077 (ACE1/2/3) constitute a triantagonistic bHLH system that competitively regulates cell elongation [24, 25].
Exogenous application of BL (BR) promotes cotton fiber cell elongation while treatment of cotton floral buds with Brz (a BR inhibitor) results in the complete absence of fiber cell differentiation, indicating that BR is required for fiber initiation and elongation [26, 27]. Besides, our previous study indicated that Gh14–3-3 proteins are involved in regulating fiber initiation and elongation through their interacting with GhBZR1 to modulate BR signalling . Also, cotton bHLH/HLH transcription factors may play important roles in fiber development [29–31]. However, little is known about how bHLH/HLH transcription factors modulate BR signaling during fiber development of cotton in detail so far. In our study, we genome-widely identified the cotton bHLH/HLH genes that may be involved in BR signaling in fiber development. Furthermore, the characters of these cotton bHLH/HLH transcription factors were approached in detail.
Characterization of cotton bHLH/HLH transcription factors
To identify the bHLH/HLH transcription factor genes in upland cotton (G. hirsutum) genome, all published bHLH/HLH gene sequences of Arabidopsis and rice were employed as queries to perform homologous blast searches against the cotton genome database (https://www.cottongen.org/tools/blast/blast) . Originally, 498 candidate bHLH/HLH genes were identified in cotton. Among them, 61 repeated sequences were discarded. Furthermore, to evaluate the reliability of the initial results, the conserved bHLH/HLH domain of predicted bHLH/HLH proteins were confirmed using the Hmmscan program and the pfam tools (http://www.ebi.ac.uk/Tools/hmmer/search/hmmscan) according to reported methods . The results showed that all the 437 putative genes have conserved bHLH or HLH domains in their sequences. Since there was no uniform annotation for the GhbHLH/HLH genes, the bHLH/HLH genes are named as GhbHLH001 to GhbHLH437 according to their chromosome locations. The average length of the newly identified bHLH/HLH proteins is 353 amino acids with variation range of 73 to 1302. The characters of the bHLH/HLH proteins including the amino acid numbers, molecular weights (MW), theoretical isoelectric points (pI) and chromosome locations were listed in Additional file 1: Table S1.
Phylogenetic relationship of cotton bHLH/HLH proteins
On the basis of the NJ phylogenetic tree, the 610 bHLH/HLH protein sequences were grouped into 26 subfamilies (including S1–S5, S7a, S7b, S9–S18 and S23–S31) (Additional file 1: Figure S1), which remain in the classification of bHLH/HLH transcription factors by Lorenzo Carretero-Paulet . Additionally, S7 and S12 were split into two subgroups (S7a and S7b, S12a and S12b), while S18, S19, S20, S21 and S22 were clustered into a single subfamily in the tree. S25, the largest group among the whole gene family groups, is composed of 61 bHLH/HLH members, occupying 14% of the total bHLH/HLH numbers, but S18 contain 2 members, being the smallest clade in the tree (Additional file 1: Table S2). The interspersed distribution of the bHLH/HLH proteins in most clades of the tree implied that the bHLH/HLH proteins expanded before the divergence of the lineages. Most of Arabidopsis bHLH/HLH genes have two or more correspondences in upland cotton genome, indicating that the divergence of cotton and Arabidopsis occurred before GhbHLH/HLH genes duplication. In subfamily 8, neither GhbHLH/HLH nor AtbHLH/HLH sequences was classified into rice bHLH/HLH sequences, which implied that this group may be lost after the divergence of monocots and dicots.
Chromosomal distribution and duplication of cotton bHLH/HLH genes
To clear the clouds on the mechanism behind the expansion of GhbHLH/HLH gene family, gene duplication events about the evolution of upland cotton genome were analyzed. 19 gene pairs in A-subgenome and 21 pairs in D-subgenome were identified respectively. These gene pairs were gathered in the same clade of the phylogenetic tree with high similarity. For example, the sequence of GhbHLH013 shares 94.5% sequence similarity with the sequence of GhbHLH127. Among these paralogous gene pairs, 18 pairs in A-subgenome and 19 pairs in D-subgenome are located on different chromosomes, indicating that segmental duplication event plays the leading role in bHLH/HLH gene family amplification during evolution, and no tandem duplication event was observed in these identified gene pairs (Fig. 2).
Structures and conserved motifs of cotton bHLH/HLH genes
To explore the motif composition in GhbHLH/HLH proteins, conserved motif sites were searched by online program MEME. Fifteen conserved motifs (named motif 1–15) were identified in the GhbHLH/HLH protein sequences (Additional file 1: Figure S2). Most of the GhbHLH/HLH proteins within the same subfamily share similar motifs, while high divergence occurs among different subfamilies, indicating that the same subfamily members may perform similar roles in cotton. For instance, the bHLH/HLHs in subfamily 1 share the conserved motif 1, 2, 3 and 4, while the members in subfamily 5 contain the conserved motifs 1, 2, 5, 6 and 7. Besides, some subfamilies have specific motifs particularly (e.g. motif 15 for subfamily 4, motif 11 for subfamily 10, and motif 13 for subfamily 26), suggesting that these motifs may lead to the specific functions of the individual subfamily. Additionally, Prosite online program was employed to annotate the functions of the identified 15 motifs. The results showed that only motif 1 and motif 2 had hits for PROSITE motifs in the database. Both of the motifs were annotated as conserved HLH domain and were uniformly observed in all GhbHLH/HLH proteins (Fig. 3b, Additional file 1: Figure S2). Collectively, the results revealed that the exon/intron patterns of GhbHLH/HLH genes and the motif compositions of GhbHLH/HLH proteins are consistent with the phylogenetic classification of GhbHLH/HLHs in cotton.
Expression of bHLH/HLH genes in fibers is induced by Brassinosteroid (BR)
The bHLH/HLH genes are differentially expressed during fiber developmental stages
GhbHLH282 plays a role in regulating plant growth by participating in response to BR signaling
It is quite difficult to identify all the bHLH/HLH protein genes completely in a certain genome, especially in allotetraploid upland cotton (G. hirsutum) genome. Besides, the diversity and complexity of bHLH/HLH gene families caused the imperfection of GhbHLH/HLH genes identification. In previous study, a set of cotton bHLH/HLH reference genes containing 289 paralogs were identified from annotated genomes of G. raimondii and G. arboreum . In our present study, we identified 437 bHLH/HLH transcription factor genes from just-completed allotetraploid G. hirsutum genome annotation, including 205 genes in A-subgenome and 232 genes in D-subgenome. The total number of GhbHLH/HLH genes is larger than that of Arabidopsis (167) and rice (177) reported . The number of bHLH/HLH genes in upland cotton is nearly 2.6 times of that in Arabidopsis, which is consistent with the fact that the protein coding genes (66,434 genes) in cotton genome is about 2.6 times of that in Arabidopsis (25,498 genes) [32, 38]. It is found that many bHLH/HLH genes in Arabidopsis have two or more counterparts in upland cotton, indicating that the amplification of bHLH/HLH genes in upland cotton may be caused by gene duplication events. Previous studies reported that the expansion of gene families is probably due to gene duplication events, consisting of tandem duplication, segmental duplication, whole genome duplication and transposition events [39, 40]. Our results suggested that the segmental duplication may be a major duplication event and contribute most to the amplification of bHLH/HLH genes in upland cotton.
Brassinosteroid (BR) is not only involved in seed germination, vascular development and senescence of tissues, but also related to cell expansion and division [41–44]. For example, BIL4 regulates cell elongation via modulating BRI1 localization for BR signal transduction . Exogenous BR application inhibits root elongation and promotes the lateral root initiation [46, 47]. Besides, in vitro studies suggested that pollen tube elongation could depend partly on BR . Unlimitedly, BR is also required for normal cotton fiber cell development [26, 27]. A recent study indicated that BR signaling promotes fiber maturation of cotton through cellulose deposition in secondary cell walls . PAG1, a cotton brassinosteroid catabolism gene, modulates fiber elongation via controlling the level of endogenous bioactive BR . Also, our previous study revealed that Gh14–3-3 proteins regulate fiber initiation and elongation by modulating BR signaling . These data indicate BR signaling plays an essential role in fiber development of cotton.
It has been reported that bHLH/HLH proteins as important regulators participate in BR signaling pathway. For instance, AtBIM2 participates in BR signaling by mediating the BR-regulated genes expression . AtAIF4 is a negative regulator of BR signaling. Overexpression of AtAIF4 results in dwarf transgenic plants, resembling BR mutants . AtPREs and AtCIB3/5 are positive regulators in promoting cell elongation by modulating BR signaling [23, 24]. Besides, AtbHLH001 (GL3) and AtbHLH002 (EGL3) positively regulate the initiation of trichomes in Arabidopsis [11, 52]. In this study, expression of GhbHLH200 was induced by BL treatment, and its transcripts were accumulated in 6–18 DPA fibers, indicating it is probably involved in cotton fiber elongation. Expression of GhbHLH109 and GhbHLH319 was inhibited by BL and induced by Brz, and its transcripts were predominantly accumulated in very early developing ovules and fibers, suggesting that these genes may have important roles in fiber initiation. Furthermore, the transcripts of GhbHLH282 were accumulated mainly in 9–15 DPA fibers, and its expression was inhibited by BL but induced by Brz. Overexpressing GhbHLH282 not only promoted plant growth, but also changed plant sensitivity to BL signaling, suggesting that GhbHLH282 may play an important role in regulating cotton fiber development via BR signaling pathway. Collectively, we identified 59 BR responsive GhbHLH/HLH genes, which are differentially expressed during fiber initiation, elongation and secondary cell wall biosynthesis stages, implying these GhbHLH/HLH genes may participate in response to BR signaling for regulating cotton fiber development.
In summary, we performed a systematic analysis of the bHLH/HLH gene family in upland cotton (G. hirsutum) genome, including gene classification, phylogenetic relationship, chromosomal distribution, gene expansion, gene structure, and motif composition, as well as gene expression pattern in fiber development and in response to BR signaling. Furthermore, our results revealed the role of GhbHLH282 in plant growth possibly via BR signaling pathway. Thus, the data reported here may facilitate a more comprehensive understanding of the specific roles of the bHLH/HLH genes in fiber development of cotton.
Upland cotton (Gossypium hirsutum) cultivar Coker312 was used in this study. Cotton plants grew in the trial field located at campus of Cental China Normal University, Wuhan, China. Flowers were tagged on the day of anthesis. Cotton bolls were harvested from the plants at 0, 3, 6, 9, 12, 15, 18 and 21 days post anthesis (DPA), respectively. Ovules and fibers at different stages were removed from the collected bolls carefully. All collected materials were frozen immediately in liquid nitrogen and stored at − 80 °C until RNA extraction.
Arabidopsis thaliana Columbia (Col-0) ecotype was used as the wild type for generating the transgenic plants. Seven-day-old seedlings grown on a half-strength MS agar medium were used as the experimental materials.
Both cotton and Arabidopsis seeds used in this study were provided by our lab.
Identification of GhbHLH/HLH transcription factors
To identify bHLH/HLH genes in upland cotton, all published bHLH/HLH gene sequences of Arabidopsis and rice were employed as queries to perform homologous blast searches against the upland cotton (G. hirsutum) genome databases (https://www.cottongen.org/tools/blast/blast) . Furthermore, the conserved domains of predicted bHLH/HLH proteins were evaluated using the hmmscan program and the pfam tools (http://www.ebi.ac.uk/Tools/hmmer/search/hmmscan) according to reported methods .
Multiple sequence alignments were conducted on the conserved bHLH/HLH domains of the identified bHLH/HLH protien sequences in upland cotton, Arabidopsis and rice genomes by Muscle aligin method using MEGA 6.0 software. Based on the results of multiple sequence alignment, MEGA 6.0 software was employed to construct an unrooted phylogenetic tree based on alignments using the NeighborJoining (NJ) method with the following parameters: No. of differences model, pairwise deletion and 1000 bootstraps . Additionally, a separate phylogenetic tree was constructed with all the conserved domains of GhbHLH/HLH protein sequences for further analysis. Then the unrooted phylogenetic tree was subjected to ITOL (http://itol.embl.de/upload.cgi) to form the interactive tree.
Analysis of chromosomal distribution and duplication of genes
To get the information about the physical locations of all GhbHLH/HLH genes on chromosomes, blastn searches against upland cotton (G. hirsutum) genome databases (https://www.cottongen.org/tools/blast/blast) were employed. Then all the GhbHLH/HLH genes were mapped on the chromosomes using CorelDRAW ×7 software except for the scaffolds genes. The GhbHLH/HLH gene duplication events were detected according to the criteria described in previous studies [54, 55]. Paralogous bHLH/HLH gene pairs were obtained based on alignment results.
Assay of gene structure and conserved motifs
The GhbHLH/HLH gene sequences and CDS sequences were identified from upland cotton (G. hirsutum) genome databases described above and were loaded into gene structure display server program (http://gsds.cbi.pku.edu.cn/) to infer the exon/intron organization of bHLH/HLH genes. To identify the conserved protein motifs, the bHLH/HLH protein sequences were submitted to online Multiple Expectation maximization for Motif Elicitation (http://meme-suite.org/tools/meme) program. The optimized MEME parameters are as follows: any number of repetitions, the optimum width from 6 to 100. The identified protein motifs were further annotated with ScanProsite.
Analysis of gene expression based on transcriptome data
To uncover the GhbHLH/HLH gene expression patterns in cotton different tissues, the RPKM (reads per kb per million reads) values which denoted the expression levels of bHLH/HLH genes were obtained from a comprehensive profile of the TM-1 transcriptome data (Accession codes, SRA: PRJNA248163, http://www.ncbi.nlm.nih.gov/sra/?term=PRJNA248163).
In vitro culture of cotton ovules
Bolls at 9 DPA (day post anthesis) from cotton plants were surface sterilized with 70% ethanol for 1 min, followed by washing with sterile water. Ovules were picked out from these sterilized bolls, and cultured in BT liquid medium containing 5 μM NAA and 0.5 μM GA3 , supplemented with 0 nM (control), 10 nM, 100 nM and 1000 nM 2,4-epibrassinolide (BL) or brassinazole2001 (Brz) at 30 °C in dark for 3 h. Then Ovules and fibers were removed from the collected bolls carefully. All collected materials were frozen immediately in liquid nitrogen and stored at − 80 °C until RNA extraction. Experiments were repeated at least three times and ran in three replicates each time.
RNA isolation and RT-PCR analysis
Total RNA was extracted from collected materials using Tiangen RNAprep Pure Plant Kit according to the manufacturer’s instructions. The total of 2 μg RNA was employed as the template for the synthesis of cDNA first-strands using M-MLV reverse transcriptase (Promega, Madison, WI) according to the manufacturer’s instructions. Gene expression levels were analyzed by real-time PCR using the fluorescent intercalating dye SYBR-Green in a detection system. The expression values of bHLH/HLH genes tested were normalized with an internal reference polyubiquitin gene (GhUBI1, access number in GenBank: EU604080). The relative expression levels (R) were calculated using the following equation: R = 2-(Ct1-Ct2), where Ct1 refers to the Ct value of bHLH/HLH genes while Ct2 is the Ct value of the reference gene. RT-PCR data are mean values and standard deviations (bar) of three independent experiments with three biological replicates. Based on the values of relative expression levels, heatmaps for gene expression patterns were generated by the online program Omicshare (http://www.omicshare.com/tools/Home/Soft/heatmap).
Gene expression levels in wild type and transgenic Arabidopsis were analyzed by semiquantitative RT-PCR analysis using the Hieff™ PCR Master Mix in 96 Well Thermal Cycler (Applied Biosystems). The expression levels of GhbHLH282 gene were tested after cDNAs were normalized with an internal reference gene Arabidopsis ACTIN2 (AF428330).
Generation of transgenic Arabidopsis plants
The coding sequence of GhbHLH282 was PCR-amplified using proofreading Pfu DNA polymerase and subsequently subcloned into the expression vector pCAMBIA-2300 under the control of the Caulifower mosaic virus (CaMV) 35S promoter. The recombinant vector construct was transferred into Agrobacterium tumefaciens GV3101 and then introduced into Arabidopsis using the floral dipping method. The transformed Arabidopsis seeds were selected on MS medium containing 50 mg/L kanamycin. Homozygous lines of T3 generations were used for phenotypic analysis.
Subcellular localization of GhbHLH282 protein
The coding sequence of GHbHLH282 was cloned into the downstream region of eGFP in the expression vector pCAMBIA-2300-35S-eGFP under the control of the Caulifower mosaic virus (CaMV) 35S promoter. The recombinant vector pCAMBIA-2300-35S-eGFP-GhbHLH282 was transferred into Agrobacterium tumefaciens GV3101 and then introduced into fully expanded leaves of tobacco (Nicotiana Benthamiana) plants using a needleless syringe. After infiltration, plants were immediately covered with plastic bags and placed at 23 °C for 48 h, and then incubated at 28 °C under a photoperiod of 16 h light/8 h dark. Tobacco foliar epidermis were stained with 4′6-diamidino-2-phenylindole (DAPI, a nucleus-specific dye) for 1 min at room temperature before observation of GFP fluorescence and DAPI staining under the confocal fluorescence microscope (Leica, Germany). The digital images were taken and processed by SP5 software (Leica, Germany).
Measurement and statistical analysis
Arabidopsis seedlings grown on a half-strength MS medium in the presence or absence of the indicated concentrations of 2,4-epibrassinolide (BL) under a photoperiod of 16 h light/8 h dark at 22 °C were photographed, and petiole and root length of these seedlings was measured using the Image J software (https://imagej.en.softonic.com/). All experiments were done at a minimum in triplicate, and the data were statistically analyzed by the Student’s t-test. More than 50 seedlings were used for each biological replicate.
All primers used are listed in Additional file 1: Table S3.
This work was supported by the National Natural Sciences Foundation of China (Grant No. 31671255), and the National Key R&D Program of China (Grant No. 2016YFD0100505).
Availability of data and materials
All data used during the current study are included in this published article or are available from the corresponding author on reasonable request.
XBL and RL conceived and designed the research, RL, JZ, DL, YLW and YW performed the experiments, RL and XBL analyzed data and wrote the paper. All authors read and approved the final manuscript.
Ethics approval and consent to participate
Cotton is a very common crop in the world. This study does not contain any research requiring ethical consent or approval.
Consent for publication
The authors declare that they have no competing interests.
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