Abstract
Background
Histone modification is an important epigenetic regulatory mechanism and essential for stress adaptation in plants. However, systematic analysis of histone modification genes (HMs) in Brassicaceae species is lacking, and their roles in response to abiotic stress have not yet been identified.
Results
In this study, we identified 102 AtHMs, 280 BnaHMs, 251 BcHMs, 251 BjHMs, 144 BnHMs, 155 BoHMs, 137 BrHMs, 122 CrHMs, and 356 CsHMs in nine Brassicaceae species, respectively. Their chromosomal locations, protein/gene structures, phylogenetic trees, and syntenies were determined. Specific domains were identified in several Brassicaceae HMs, indicating an association with diverse functions. Syntenic analysis showed that the expansion of Brassicaceae HMs may be due to segmental and whole-genome duplications. Nine key BnaHMs in allotetraploid rapeseed may be responsible for ammonium, salt, boron, cadmium, nitrate, and potassium stress based on co-expression network analysis. According to weighted gene co-expression network analysis (WGCNA), 12 BnaHMs were associated with stress adaptation. Among the above genes, BnaPRMT11 simultaneously responded to four different stresses based on differential expression analysis, while BnaSDG46, BnaHDT10, and BnaHDA1 participated in five stresses. BnaSDG46 was also involved in four different stresses based on WGCNA, while BnaSDG10 and BnaJMJ58 were differentially expressed in response to six different stresses. In summary, six candidate genes for stress resistance (BnaPRMT11, BnaSDG46, BnaSDG10, BnaJMJ58, BnaHDT10, and BnaHDA1) were identified.
Conclusions
Taken together, these findings help clarify the biological roles of Brassicaceae HMs. The identified candidate genes provide an important reference for the potential development of stress-tolerant oilseed plants.
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Background
Histone modification (HM) is an epigenetic regulatory mechanism that plays crucial roles in various aspects of plant growth and stress response by activating or silencing gene expression [1,2,3,4]. HM genes (HMs) include histone methyltransferases (HMTs), histone demethylases (HDMs), histone acetylases (HATs), and histone deacetylases (HDACs) [5,6,7,8].
HMTs are encoded by the SET-domain group (SDG) and protein arginine methyltransferase (PRMT) genes and catalyze HM [9]. Methylation and environmental factors are related to stress, which affects gene expression by changing methylation levels and stress resistance [10]. Several processes, such as fungal pathogen resistance, shoot and root branching, circadian cycle, hormone regulation, abscisic acid (ABA) morphogenesis, and salt stress, are affected by HMTs [11, 12]. For example, AtSDG8 is involved in the regulation of shoot meristem activity, while AtSDG26 and AtPRMT10 are involved in the regulation of flowering in Arabidopsis [13,14,15]. Histone modification can be erased by HDMs, including lysine-specific demethylase 1 (LSD1) and Jumonji C (JmjC) domain containing proteins [16,17,18]. HDMs function in brassinosteroid (BR) signaling, pollen development, chromatin regulation, floral induction, and floral organ formation [19, 20]. In Arabidopsis, JMJ30 expression changes in response to environmental stimuli, e.g., enhancement by salt and heat stress [21, 22], and flower repressor JMJ13 can be affected by temperature and photoperiod [23]. HATs and HDACs catalyze the transfer of acetyl groups from acetyl-CoA to lysine residues [24, 25]. HATs and HDACs participate in the regulation of developmental transition, environmental signal responses, reproductive development, and gene silencing [26,27,28]. For example, HAC1 inactivation affects both vegetative and reproductive development in Arabidopsis [29], AtSRT2 regulates salt tolerance during seed germination [30], and AtHDT4 participates in abiotic stress responses [31]. Previous studies have suggested that modifications affect functions, including transcriptional regulation of other genes in yeast [32].
Abiotic stress, such salinity, inappropriate nutrition, and metal toxicity, can adversely affect crop growth and yield [33, 34]. Nutrient imbalances, membrane damage, and dysfunctional antioxidant system can occur under soil salinization [35]. Various nutrients are essential for optimal plant growth and yield. Nitrogen (N) is a macronutrient “life element” that strongly affects plant growth and development [36], while excess ammonium (NH4+), an inorganic N nutrient, is toxic to plants [37]. Phosphorus (P) shares essential roles in regulating plant energy metabolism, and its deficiency can reduce cell division and elongation in grass leaves [38]. Potassium (K) is a vital macronutrient for plant growth and organ development, and participates in many physiological processes, such as osmoregulation. Moreover, K + transport participates in abiotic stress responses [39, 40]. Boron (B) is a micronutrient essential for the transport of carbohydrates, although both excess and deficiency can adversely impact crop growth and yield [41, 42]. Plants can also be affected by non-essential heavy metals, such as cadmium (Cd), which is highly biotoxic and easily absorbed by plants through sewage effluent, industrial waste, and agricultural run-off [43].
Brassicaceae plants are important and economically valuable crops, noted for their oil production [44, 45]. Given their immobility, plants are unable to avoid abiotic and biotic stresses, which can impair growth, development, and production. However, plants can adapt to stress by activating a series of physiological and molecular mechanisms, such as HM [46, 47]. Therefore, improving stress resistance and yield in Brassicaceae plants is a key goal of breeding [48]. To date, however, few studies have explored the regulation of gene expression related to stress resistance or conducted systematic study of HMs in Brassicaceae species. Here, we conducted a comprehensive study of HMs in nine Brassicaceae species, including Arabidopsis thaliana, Brassica napus, Brassica carinata, Brassica juncea, Brassica nigra, Brassica oleracea, Brassica rapa, Capsella rubella, and Camelina sativa. We further determined their chromosomal locations, conserved domains, gene structures, phylogenetic relationships, and syntenies. The responses of HMs to NH4+ toxicity, B deficiency and excess, Cd exposure, K shortage, N limitation, P starvation, and salt stress were explored in allotetraploid rapeseed. Potential candidate BnaHMs that responded to the above stresses were also identified. This study provides important clues for understanding the Brassicaceae HM gene family.
Results
Genome-wide identification of Brassicaceae HMs and their phylogenetic analysis
In the present study, we identified 1 798 HMs, including 102, 280, 251, 251, 144, 155, 137, 122, and 356 in (A) thaliana, (B) napus, B. carinata, B. juncea, B. nigra, B. oleracea, B. rapa, (C) rubella, and C. sativa (Figure S1 and Table S1). The number of HMTs, HDMs, HATs, and HDACs varied among species, with 2.7-, 2.5-, 2.5-, and 3.5-fold as many BnaHMs, BcaHMs, BjuHMs, and CsHMs as AtHMs, respectively (Figure S1a). There were 47–159 SDGs, 7–27 PRMTs, 2–8 HDMAs, 20–77 JMJs, 3–10 HAGs, 1–7 HAMs, 4–10 HACs, 1–4 HAFs, 12–40 HDAs, 2–8 SRTs, and 4–16 HDTs in the above Brassicaceae species, respectively (Figure S1b), named according on their chromosomal position in each species (Figure S2).
To elucidate the evolutionary relationships among HMs, unrooted phylogenetic trees were constructed. Generally, each type of HAT, HDAC, HDM, and HMT shared relatively close relationships in distinct groups, with some exceptions (Figure S3). For example, in terms of HATs, all HACs were in group a, most HAGs were in group b, and HAFs and HAMs were in groups c and d, respectively (Figure S3-1).
Conserved domain, structure, and synteny analysis of HMs
Diverse conserved domains were identified in the different HMs (Figure S4) and the number of conserved motifs was determined in the Arabidopsis HMs (Figure S4-1). Most conserved domains in the Arabidopsis HMs were also present in the non-model plants (B. napus, B. carinata, B. juncea, B. nigra, B. oleracea, B. rapa, C. rubella, and C. sativa). However, several distinct domains were identified in the non-model Brassicaceae HMs (Figure S4), including the SHOCT domain in BjHDA10 and BjHDT11, which may bind to itself to perform important functions as an oligomerization domain or bind to other protein domains/motifs and nucleic acids [49]. BjHDA24 shares a domain with the CYCLIN superfamily, which functions in the cell cycle and transcriptional control (Figure S4-8). In general, each class of HM shared a similar gene structure. Of note, several HMs, including BoJMJ23, BoSDG24, and BcJMJ54, contained long introns (Figure S4).
To determine the expansion patterns of HMs, duplication events within gene pairs were investigated in duplicated blocks of each Brassicaceae genome. In total, 1 176 gene pairs were identified, including 11, 256, 194, 215, 49, 55, 42, 15, and 339 pairs in (A) thaliana, (B) napus, B. carinata, B. juncea, B. nigra, B. oleracea, B. rapa, (C) rubella, and C. sativa, respectively (Figure S5 and Table S2). To understand the potential roles of unknown Brassicaceae HM genes, collinearity analysis was performed between Arabidopsis and non-model Brassicaceae species. In total, 151, 157, 178, 101, 89, 216, 83, and 109 gene pairs were identified in A. thaliana-B. carinata, A. thaliana-B. juncea, A. thaliana-B. napus, A. thaliana-B. oleracea, A. thaliana-B. rapa, A. thaliana-C. sativa, A. thaliana-C. rubella, and A. thaliana-B. nigra, respectively (Figure S6 and Table S3).
Effects of NH4+, salt, B, and Cd on expression patterns of BnaHMs
Although NH4+ is the main N source for plants, excess can cause toxicity to crops and reduce grain yields [50, 51]. Here, the expression profiles of BnaHM genes were investigated to predict their potential involvement in NH4+ toxicity resistance. In roots, 12 BnaHMs were differentially expressed after excess NH4+ treatment, half of which were up-regulated (Fig. 1a). In shoots, 37 BnaHMs were differentially expressed, six of which showed low levels in the NH4+-treated group (Fig. 1b). Among these differentially expressed genes (DEGs), based on gene co-expression network analysis (GCNA), BnaPRMT11 and HDT10 may be critical genes in response to NH4+ toxicity (Fig. 1c). In roots, 15 and 38 BnaHMs were suppressed and induced by salt treatment, respectively (Fig. 1d), with BnaHDA11 and BnaPRMT8 potentially playing roles in salt adaptation (Fig. 1e). In shoots, 48 BnaHMs, especially BnaSDG58, were markedly regulated by salt exposure (Fig. 1f). According to GCNA, BnaHDT10 was identified as a hub gene in response to salt stress (Fig. 1g).
Both B deficiency and toxicity can have adverse effects on plant growth and development [52]. However, whether BnaHMs are involved in B-mediated plant growth is unclear. Our results identified several BnaHMs that were differentially expressed after B treatment (Fig. 2). In roots, BnaHDA3 and BnaSDG46 were inhibited by B deficiency, while five BnaHMs were induced (Fig. 2a). B toxicity also altered the expression patterns of BnaHMs (Fig. 2b, e). In the B deficiency group, BnaJMJ18, BnaSDG82, and BnaJMJ9 were up-regulated in shoots, while 69 BnaHMs were down-regulated (Fig. 2c). BnaSDG4 was identified as a key gene (Fig. 2d). In shoots, only BnaHDA12 increased in response to excess B, while the remaining BnaHMs were reduced (Fig. 2e). Among them, BnaSDG94 was identified as a potential hub gene (Fig. 2f).
Cd is a non-essential heavy metal toxic for plant growth [53]. In roots, 15 and six BnaHMs exhibited higher and lower expression, respectively, in the Cd-treated group compared with the control group (Fig. 3a). In shoots, BnaSDG30 and BnaSDG75 were significantly inhibited by Cd, while BnaHDT2 was induced (Fig. 3d). BnaSDG75 was also identified as a key gene in the co-expression network (Fig. 3e).
Effects of N, K, and P on expression patterns of BnaHMs
As an essential macronutrient, N is required for rapeseed growth and development [54]. To investigate the response of BnaHMs to N limitation, we identified their expression profiles. BnaSDG4, BnaJMJ9, and BnaJMJ43 were up-regulated in the N-treated roots, while nine other genes were down-regulated (Fig. 3b). In shoots, BnaPRMT10, BnaHAF1, BnaHDA27, BnaHDA11, and BnaSDG23 were substantially induced by N deficiency, while BnaSDG43, BnaJMJ13, BnaSDG102, and BnaJMJ61 were repressed (Fig. 3c).
Previous studies have shown that K can also cause stress to plants [55, 56]. Our results showed that limited K induced 11 BnaHMs and suppressed seven BnaHMs in the roots, especially BnaSDG81 (Fig. 4a). In shoots, 10 BnaHMs (e.g., BnaHDA15, BnaSDG46, and BnaSDG1) were decreased after K treatment, while 52 BnaHMs, especially BnaJMJ47, BnaSDG86, and BnaSDG88, were increased (Fig. 4d). BnaHDA15 was identified as a key gene according to GCNA (Fig. 4e). Given its close involvement in photosynthesis, P is an essential nutrient for plant growth and development [57]. Here, in response to P stress, the expression levels of several BnaHMs, especially BnaJMJ6, increased in roots, whereas five BnaHMs were markedly suppressed (Fig. 4b). In shoots, 14 BnaHMs showed higher expression levels after P treatment, while 29 were inhibited by P stress (Fig. 4c).
Identification of weighted gene co-expression network analysis (WGCNA) modules and hub genes associated with target traits
All genes in the RNA sequencing (RNA-seq) data, not just DEGs, were analyzed for significant associations with phenotypes using WGCNA based on previous methods [58]. WGCNA was established to analyze hub genes in response to A, salt, Cd, N, and K stress.
The “lightyellow” (r = -0.64, p < 0.01) and “turquoise” (r = -0.92, p < 0.01) modules were negatively correlated with chlorophyll content (SPAD) after NH4+ toxicity treatment (Fig. 5a). Two co-expression networks were constructed to identify core genes. In the “lightyellow” and “turquoise” modules, BnaPRMT15, and BnaSDG64, BnaSDG53, and BnaSDG36 were respectively identified in response to NH4+ exposure (Fig. 5b, c). In total, 37 genes in the “lightyellow” module and 40 genes in the “turquoise” module are involved in various stresses, such as oxidative stress, and interact with core genes (Table S5-1).
WGCNA was also performed to evaluate the relationship between modules and salinity (Fig. 6). The “salmon” (r = -0.83, p < 0.05) and “blue” (r = -0.91, p < 0.05) modules were negatively correlated with biomass and leaf area, respectively (Fig. 6a). Four BnaHMs (BnaSDG53, BnaSDG36, BnaSDG46, and BnaSDG64) were identified as important genes in the “blue” module (Fig. 6b). BnaHAG3, BnaHDA12, BnaHDA8, and BnaHAG7 were identified as hub genes in the “salmon” module (Fig. 6c). In addition, seven and nine genes in the “salmon” and “blue” modules, respectively, were salt-responsive and associated with core genes (Table S5-2).
Using WGCNA, core genes associated with Cd stress were identified. As shown in Fig. 7, both “green” and “purple” module were negatively correlated with SPAD and positively correlated with biomass (Fig. 7a). “Yellow” module was too, while “dark turquoise” was negatively correlated with SPAD and “purple” was positively correlated with biomass (Fig. 7a). Gene interaction networks were established for these two modules, and two key genes were identified (BnaSDG46 and BnaPRMT4, respectively) (Fig. 7b, c). In both modules, several Cd-resistance genes were identified and were associated with core genes (Table S5-3).
The relationship between WGCNA modules and N shortage was also explored. All genes were clustered into seven modules, and genes in the “green” module (r = -0.83, p < 0.05) were significantly correlated with SPAD (Fig. 8a). Three hub genes (BnaSDG53, BnaHDA1, and BnaSDG46) were screened from co-expression gene network mapping (Fig. 8b) and may play additional roles in adaptation to various stresses. Furthermore, several genes in the “green” module play roles in stress adaptation and interact with the three hub genes (Table S5-4).
In response to K stress, eight WGCNA modules were obtained. The “turquoise” module (r = -0.92, p < 0.05) showed a negative correlation with SPAD (Fig. 9a). BnaSDG60 and BnaSDG46 were identified as critical genes in this module (Fig. 9b). In addition, stress-related and K-transport genes in the ‘turquoise” module were associated with BnaSDG60 and BnaSDG46 (Table S5-5).
Diverse responses of BnaHMs to nutrient stresses
To investigate whether BnaHMs responded to diverse stresses simultaneously, we constructed a Venn diagram. Results showed that most BnaHMs were affected by more than one stress (Fig. 10 and Table S4). For example, 27 BnaHMs were simultaneously under the control of two stresses; 31 BnaHMs simultaneously responded to three stress signals; 32 BnaHMs simultaneously responded to four stresses; 11 BnaHMs were controlled by five stresses; and two genes responded to six stresses.
Discussion
HMs play essential roles in plant growth and stress responses and have been successfully identified in many plants, such as Arabidopsis, wheat, and maize [59]. However, information on Brassicaceae HMs remains limited. In this study, we systematically characterized HMs in nine Brassicaceae species and identified 1 798 HMs, including 102 AtHMs, 280 BnaHMs, 251 BcHMs, 251 BjHMs, 144 BnHMs, 155 BoHMs, 137 BrHMs, 122 CrHMs, and 356 CsHMs. We further analyzed their phylogeny, conserved domains, gene structure, and synteny, as well as their expression profiles in response to NH4+, B, salt, Cd, N, P, and K stress. These results will contribute to a comprehensive understanding of Brassicaceae HM genes.
Comparison of HMs among nine Brassicaceae species
We identified 280, 251, 251, 144, 155, 137, 122, and 356 HMs in B. napus, B. carinata, B. juncea, B. nigra, B. oleracea, B. rapa, Capsella rubella, and Camelina sativa, respectively (Figure S1 and Table S1). We also found significantly more BnaHMs, BcHMs, BjHMs, BnHMs, BoHMs, BrHMs, CrHMs, and CsHMs than AtHMs (2.7-, 2.4-, 2.4-, 1.4-, 1.5-,1.3-, 1.1-, and 3.4-fold higher, respectively) (Figure S1 and Table S1). Orthologous HMs were found based on synteny analysis. We identified 11 AtHM, 256 BnaHM, 194 BcHM, 215 BjHM, 49 BnHM, 55 BoHM, 42 BrHM,15 CrHM, and 339 CsHM pairs (Figure S5 and Table S2). Results showed that more segmental duplications of HMs were found in non-model Brassicaceae species than in Arabidopsis, which may induce the expression of non-model Brassicaceae HMs. Whole-genome replication is known to occur in B. napus, B. carinata, B. juncea, and Camelina sativa [60,61,62,63,64]. Therefore, segmental and whole-genome duplications may have contributed to the expansion and evolution of HMs in the above species.
Synteny analysis between duplicated blocks of Arabidopsis-B. carinata, Arabidopsis-B. juncea, Arabidopsis-B. napus, Arabidopsis-B. oleracea, Arabidopsis-B. rapa, Arabidopsis-C.sativa, Arabidopsis-C. rubella, and Arabidopsis-B. nigra was also performed, yielding 151, 157, 178, 101, 89, 216, 83 and 109 gene pairs, respectively (Figure S6 and Table S3). These gene pairs are considered to have originated from common ancestors with AtHMs [60,61,62,63,64], suggesting that they may have similar functions to the corresponding Arabidopsis genes. Thus, the functions of non-model Brassicaceae HMs were predicted based on homologous Arabidopsis HMs. Several AtHMs are involved in stress responses [10, 65, 66]. Although many unknown non-model Brassicaceae HMs could be inferred from orthologous Arabidopsis genes, these comparisons require further experiments.
Conserved domains are associated with gene function [67]. We identified typical domains in the HMs (Figure S4). Most Brassicaceae HMs with conserved domains shared similar functions, but several distinct domains were identified in several non-model Brassicaceae HMs, such as the FYVE_like_SF superfamily domain in BnaJMJ65, which plays an important role in vesicular traffic and signal transduction (Figure S4-2). Novel functions may be predicted from unique domains, and thus greater attention should be paid to genes with special elements in the future.
Putative functions of BnaHMs in stress response
HMs are important in plant defense. Here, the expression patterns of BnaHMs were determined to explore their function under various stresses. In roots and shoots, 79 and 81 BnaHMs were up-regulated or down-regulated by B deficiency and toxicity (Fig. 2) and BnaHM expression patterns were changed by NH4+ and N deficiency (Figs. 1a-c and 3b-c). More than 50 BnaHMs showed differential expression in response to P shortage, and many BnaHMs were influenced by K deficiency stress (Fig. 4). These findings indicate that BnaHMs play essential roles in the stress response. Various abiotic stresses, including drought, salinity, and cold, adversely affect plant growth and development. HMs share important roles in regulating stress adaptation. For example, AtHDA6 and AtHDA19 are involved in ABA responses and are required for salt tolerance [59, 68]. Here, many BnaHMs responded to Cd and salt stress, with altered expression in the roots or shoots (Figs. 1d-g and 3d-e). These findings suggest that BnaHMs and methylation play essential roles in rapeseed resistance to diverse stresses.
Candidate BnaHMs were determined through DEG co-expression analysis and WGCNA. BnaPRMT15, BnaSDG36, BnaSDG53, BnaSDG64, BnaHDT10, and BnaPRMT11 were identified in response to NH4+ toxicity (Figs. 1c and 5). BnaHDA11, BnaHDT10, BnaPRMT8, BnaHAG3, BnaHAG7, BnaSDG36, BnaSDG46, BnaSDG53, BnaHDA12, BnaHDA8, and BnaSDG64 were associated with plant survival under salt stress (Fig. 1e and g, and Fig. 6). BnaPRMT4, BnaSDG46, and BnaSDG75 were identified as Cd-related genes (Figs. 3e and 7). BnaSDG4 and BnaSDG94 were identified as B stress candidate genes (Fig. 2d and f). BnaSDG46, BnaSDG53, and BnaHDA1 were identified as N-deficiency candidate genes (Fig. 8). BnaHDA15, BnaSDG46, and BnaSDG60 were identified as K limitation-related genes (Fig. 9). Based on orthologous gene analysis, the ortholog of AtHDA6, which responds to drought stress [69], was identified as BnaHDA8, and the ortholog of AtHDA14, which functions in regulating stress responses [70,71,72,73,74], was identified as BnaHDA1. In addition, according to WGCNA, several downstream genes identified in modules that may be involved in various stresses, such as low temperature and salt, interacted with the core genes, indicating that these core genes may participate in stress tolerance by interacting with downstream stress-related genes (Table S5). These results suggest that HMs play an important role in stress response. As such, future studies should pay attention to the above candidate genes.
This study also found that many differentially expressed BnaHMs responded to different stresses at the same time (Table S4). For example, two BnaHMs (BnaSDG10 and BnaJMJ58) were simultaneously regulated by six stresses, and 11 BnaHMs (e.g., BnaHDT10, BnaSDG46, BnaPRMT10) were simultaneously regulated by five stresses. However, certain genes were only impacted by a single stress signal, implying that many BnaHMs may participant in different stresses, while others only play a core role under a specific stress.
Previous studies have shown that several HMs in rice may participate in stress adaptations. For example, OsHDT701 and OsHDT702 in rice are repressed by drought and salt simultaneously [75, 76]. Here, several key genes identified by co-expression analysis or WGCNA also responded to more than three different types of stress. For instance, BnaPRMT11and BnaHDA1 were differentially expressed under four and five types of stress, respectively (Fig. 10 and Table S4) and BnaSDG10 and BnaJMJ58 simultaneously responded to six different stresses. The salt stress-correlated core gene BnaHDT10 also responded to four other stresses (i.e., A, B, Cd, and P). In addition, BnaSDG46 was identified as a salt-, B-, Cd- and K-related key gene by WGCNA. These results suggest that the above hub BnaHMs may play critical roles in resistance to multiple stressors, and that they may show different functions under different stress. Therefore, future studies should focus on the potential functions of these genes.
Methods
HM gene identification, phylogenetic relationship, chromosomal location, conserved domains, gene structure, and synteny
Known AtHM protein sequences were used as queries and the B. napus, B. carinata, B. juncea, B. nigra, B. oleracea, B. rapa, C. rubella, and C. sativa protein databases were searched using “Blast Several Sequences to a Big Database” in TBtools [77] with an e-value of e-5. After aligning the full-length protein sequences by ClustalW with default parameters, MEGA X was used to construct the phylogenetic tree with the maximum-likelihood method [78].
Using chromosome length and gene position files, the chromosomal distributions of HMs were acquired and visualized using “Gene Location Visualize (Advanced)” in TBtools. The conserved domains in HMs were confirmed using the Batch Web CD-Search Tool (https://www.ncbi.nlm.nih.gov/Structure/bwrpsb/bwrpsb.cgi) [77]. The conserved domains were visualized using “Visualize NCBI CDD Domain Pattern” in TBtools [77]. The Visualize Gene Structure (Basic) tool was used to draw the gene structure map based on generic feature format v3 (gff3) files of the HMs.
We used “One Step MCScanX” in TBtools to analyze HM duplication events with genome sequences and gff3 files. “Table Row Extract or Filter”, “File Transformat for Microsynteny Viewer and Advanced Circos”, “Fasta stats”, and “File Merge for MCScanX” in TBtools were used to visualize the syntenic relationships of HM genes based on previous studies [77].
Transcriptome analysis, GCNA, and WGCNA of BnaHMs
The transcriptome data can be found in previously published papers [79,80,81,82,83]. All data required to reproduce these findings can be obtained by contacting the correlation authors. Fastp software (v0.20.1) was used to evaluate the overall sequencing quality of the raw reads and low-quality reads were removed. Alignment of high-quality reads with B. napus reference genome sequences (http://cbi.hzau.edu.cn/cgi-bin/rape/download_ext, accessed on 15 May 2022) was performed using Hisat2 (v2.1.0) and SAMtools (v1.6) software. Stringtie (v1.3.3b) was used to calculate the expression levels of high-confidence genes in each sample. The R package “edgeR”, with p < 0.05, false-discovery rate (FDR) < 0.05, and |log2(fold-change)| ≥ 1, was used to define DEGs. GCNA was performed using the cor.test function in R (v4.1), and network visualized using Cytoscape (v3.8.2, https://cytoscape.org/download.html, accessed on 13 April 2022) [56]. The R WGCNA package (v1.51) was used to complete WGCNA with high-quality genes. Significant module-trait relationships with target traits were determined by calculating modular trait gene values. Gene co-expression network maps were generated using Cytoscape (v3.8.2, https://cytoscape.org/download.html, accessed on 13 April 2022). The gene with high | log2 (a fold - change) | and degree are selected as hub gene, and was placed in the middle of the network.
Plant materials and treatments
Uniform 7-day-old B. napus (Zhongshuang 11) seedings were transplanted into black plastic containers containing Hoagland nutrient solution (5.0 mM KNO3, 1.0 mM KH2PO4, 2.0 mM MgSO4·7H2O, 5.0 mM Ca (NO3)2·4H2O, 0.10 µM Na2MoO4·2H2O, 0.050 mM EDTA-Fe, 0.80 µM ZnSO4·7H2O, 9.0 µM MnCl2·4H2O, 0.30 µM CuSO4·5H2O, and 46 µM H3BO3). Before treatments, the B. napus seedlings were cultivated for 10 days (d) in a chamber under 25 °C daytime/22°C night-time temperature, 300–320 µmol m− 2 s− 1 light intensity, 16-h light/8-h dark photoperiod, and 70% relative humidity. B deficiency and toxicity treatments: We cultivated 17-day-old seedlings for 10 d in B-deficient (0.25 µM H3BO3) and B-excess (1 500 µM H3BO3) treatment groups; N, P, and K depletion treatments: We cultivated 17-day-old B. napus seedlings in Hoagland nutrient solution (consisting of 0.30 mM N, 5 mΜ P, and 0.30 mM K) for 3 d; NH4+toxicity treatment: We cultivated 17-day-old uniform Zhongshuang 11 seedlings in Hoagland nutrient solution (consisting of normal nitrate) for 10 d, followed by transfer to a N-free solution for 3 d, and final exposure to 9.0 mM NH4+ (excess NH4+) for 6 h; Cd toxicity and salt treatments: For Cd- and salt-treatment, we cultivated 17-day-old Zhongshuang 11 seedlings in 10 µM CdCl2 and 200 mM NaCl for 12 h and 1 d, respectively. The seedlings in the control groups were cultivated in a normal solution for the appropriate times based on the aforementioned treatments. Transcriptome sequencing was performed using roots and shoots from control and stress-treated plants as described above [84,85,86].
Conclusions
In this study, 1 798 HM genes were systematically identified in nine Brassicaceae species. Their chromosomal locations, protein/gene structure, and phylogenetic and syntenic relationships were characterized. The BnaHMs responding to A, salt, Cd, N, and K stress were investigated through differential expression analysis (GCNA and WGCNA). Taken together, BnaPRMT11, BnaJMJ58, BnaSDG46, BnaHDA1, BnaSDG10, and BnaHDT10, were identified as potential hub genes, especially BnaSDG46 and BnaHDT10. Our results suggest that BnaHMs may be crucial for regulating stress adaptation in rapeseed. The candidate genes identified here should be validated in future studies.
Data Availability
The raw transcriptome sequencing data were submitted to the National Centre for Biotechnology Information (NCBI) (http://www.ncbi.nlm.nih.gov/) under BioProject PRJNA340053, PRJNA718104, and PRJCA001323. The datasets used and/or analyzed in the current study are available from the corresponding author upon reasonable request.
Abbreviations
- HMs :
-
Histone modification genes
- NH4 + :
-
Ammonium
- Cd:
-
Cadmium
- B:
-
Boron
- N:
-
Nitrogen
- K:
-
Potassium
- P:
-
Phosphate
- DEGs:
-
Differentially expressed genes
- WGCNA:
-
Weighted gene co-expression network analysis
- GCNA:
-
Gene co-expression network analysis.
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This work was supported by the Chinese Postdoctoral Science Foundation (2021M692944), Research Start-Up Project (32212399 and 32213006), Famous Teachers in Central Plains (22610002), and Application of Molecular Design Breeding of Oil Crops and Intelligent Auxiliary Information System in Supercomputing Ecology, Henan Key Project of Science and Technology (202102110006).
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HLL and HYP was involved in data analysis. MSJ, ZXL and ZKY made the experiments. ZLW, HYP and HJY designed the study. HLL and ZLW wrote the manuscript. All the authors read and approved the final version of the manuscript.
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Hu, LL., Zheng, LW., Zhu, XL. et al. Genome-wide identification of Brassicaceae histone modification genes and their responses to abiotic stresses in allotetraploid rapeseed. BMC Plant Biol 23, 248 (2023). https://doi.org/10.1186/s12870-023-04256-1
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DOI: https://doi.org/10.1186/s12870-023-04256-1