Skip to main content

ORIGINAL RESEARCH article

Front. Plant Sci., 19 September 2024
Sec. Plant Systematics and Evolution

Extensive transcriptome data providing great efficacy in genetic research and adaptive gene discovery: a case study of Elymus sibiricus L. (Poaceae, Triticeae)

  • 1College of Grassland Science and Technology, Sichuan Agricultural University, Chengdu, Sichuan, China
  • 2Sichuan Academy of Grassland Sciences, Chengdu, Sichuan, China

Genetic markers play a central role in understanding genetic diversity, speciation, evolutionary processes, and how species respond to environmental stresses. However, conventional molecular markers are less effective when studying polyploid species with large genomes. In this study, we compared gene expression levels in 101 accessions of Elymus sibiricus, a widely distributed allotetraploid forage species across the Eurasian continent. A total of 20,273 high quality transcriptomic SNPs were identified. In addition, 72,344 evolutionary information loci of these accessions of E. sibiricus were identified using genome skimming data in conjunction with the assembled composite genome. The population structure results suggest that transcriptome SNPs were more effective than SNPs derived from genome skimming data in revealing the population structure of E. sibiricus from different locations, and also outperformed gene expression levels. Compared with transcriptome SNPs, the investigation of population-specifically-expressed genes (PSEGs) using expression levels revealed a larger number of locally adapted genes mainly involved in the ion response process in the Sichuan, Inner Mongolia, and Xizang geographical groups. Furthermore, we performed the weighted gene co-expression network analysis (WGCNA) and successfully identified potential regulators of PSEGs. Therefore, for species lacking genomic information, the use of transcriptome SNPs is an efficient approach to perform population structure analysis. In addition, analyzing genes under selection through nucleotide diversity and genetic differentiation index analysis based on transcriptome SNPs, and exploring PSEG through expression levels is an effective method for analyzing locally adaptive genes.

Introduction

Local adaptation occurs when divergent selection outweighs random genetic drift and the equalizing effect of gene flow between populations (Kawecki and Ebert, 2004). These premises suggest that certain widely distributed wild plants show distinctive local adaptations caused by restricted gene flow between populations due to geographical and environmental isolation. Multiple selection factors interact with geographic distance between populations to shape the evolutionary dynamics of species by restricting gene flow (López-Goldar and Agrawal, 2021). In addition to the molecular perspective and adaptive effects, a comprehensive study of local adaptation in species should also consider ecological factors and the co-evolution of plants and their environment. For example, local adaptation along natural gradients such as latitude and altitude, which have been extensively studied, may be the result of the combined influences of different ecological effects on selection and gene flow (López-Goldar and Agrawal, 2021; Tiffin and Ross-Ibarra, 2014).

Compared to neutral regions, where selection is not expected, regions of genes and linked loci under divergent selection are expected to experience stronger selection pressures (Limborg et al., 2012). The adaptive significance of existing polymorphic sites is often difficult to estimate, as they may not be the direct targets of selection, but rather by-products of hitchhiking effects (Zhang et al., 2024). Large-scale transcriptome sequencing can help us study functional genetic variation, thereby increasing the chances of detecting natural selection, as functional genetic variation is expected to be more directly influenced by natural selection and result in a population-specific expression (Tang et al., 2021). The regulation of gene expression is a complex and intricate process, and studies of the evolution of gene expression have shown significant variability in the variability of regulatory elements both within and between natural populations (Shi et al., 2012). However, studying adaptive evolution at the level of gene expression is only relevant for specific genes or sets of co-expression gene. Given that the environment always influences gene expression, this implies that general evolutionary patterns of gene expression are not necessarily adaptive (Signor and Nuzhdin, 2018). Common garden experiments test how heritable traits are influenced by natural selection (leading to natural variation) and ultimately affect optimal outcomes for population persistence (Schwinning et al., 2022). The natural variation observed could be attributed to the prolonged acclimatization processes that occur in response to the particular environmental conditions of the sites where the species occur.

Elymus sibiricus, the model species of the genus Elymus, is widely distributed across the Eurasian continent and exhibits significant genetic diversity and phenotypic variance (Xiong et al., 2021). The extensive habitat diversity has contributed to the unique adaptability of E. sibiricus ecotypes across different geographic groups (Han et al., 2022). Due to its remarkable adaptability to the high altitude environment, superior nutritional value and ease of cultivation, E. sibiricus is the dominant forage crop and is extensively cultivated in the artificial forage grasslands of the Qinghai-Tibetan Plateau. Nevertheless, the unavailability of the reference genome hampers genetic research on E. sibiricus, resulting in previous studies relying solely on molecular markers such as genomic SSRs (Xiong et al., 2021; Lei et al., 2014), EST-SSRs (Zhang et al., 2019; Zheng et al., 2020), and chloroplast/mitochondrial SSRs (Lei et al., 2014; Xiong et al., 2022), to investigate the population structure and adaptive evolution of the species. Due to their limited coverage, these markers can only reveal specific genetic variations. Considering their larger number and wider distribution, SNP markers are more suitable for population genetic research (Sun et al., 2020). Some SNPs derived from simplified genome sequencing have been used to study the population structure of E. sibiricus (Han et al., 2022). However, a significant proportion of these markers are located in non-functional regions. Furthermore, mapping SNPs located in genic regions to specific genes is challenging due to the lack of comprehensive reference genomic information. In this context, the use of transcriptome data allows a thorough investigation of functional regions and genes associated with adaptive traits, and the detection of sequence variation and expression levels within these regions. SNP-based studies of the transcriptome can provide a wealth of SNP markers, and these variants can affect the coding sequence of proteins, thus affecting gene expression and function. In addition, the abundance of SNP markers in the transcriptome allows accurate assessment of genetic variation and population structure (Yang, 1998). However, issues of widespread purifying selection in the transcriptome and concerns about sample size point to the need for comparisons between mRNA and established DNA-based methods (Thorstensen et al., 2020; Pratlong et al., 2015; Thorstensen et al., 2021). Genome skimming sequencing is a cost-effective protocol for obtaining genome-level variation and has shown excellent potential for phylogenetics, species identification, and genetic diversity assessment (Richter et al., 2015; Trevisan et al., 2019). Furthermore, SISRS software allows the identification of phylogenetically informative sites across the genome by skimming sequencing data without reference genome information (Schwartz et al., 2015; Literman et al., 2023), allowing us to perform population variation calling at the DNA level.

This study included 101 wild E. sibiricus accessions from both domestic and international sources, covering the primary distribution regions of E. sibiricus. The transcriptomes of these collected accessions were sequenced, and the full-length transcriptome of E. sibiricus was assembled using previous research data to construct a reference sequence. The aims of this study included: (1) studying population genetic analysis using transcriptome SNPs and expression levels; (2) analyzing population (geo-group)-specific expression genes (PSEG), investigating genes related to adaptability of E. sibiricus; (3) using genome skimming data from 101 accessions as reported by Xiong et al. (2023) to identify homologous sequences at the genome level (Schwartz et al., 2015) and compare their effectiveness in population structure studies with transcriptome data (both transcriptome SNPs and expression levels). This study provides a comprehensive analysis of the population structure of E. sibiricus, including transcriptome SNPs, expression levels and genome-level homologous sequences, which could provide a genetic research mode in polyploid species without genomic information. It will also identify the functional genes that contribute to the differentiation of geographic groups of E. sibiricus.

Results

Full-length transcriptome assembly, SNPs calling from the transcriptome and genome skimming data

The reference transcriptome of E. sibiricus was assembled, comprising 6982 contigs with an N50 of 42,573 bp and a GC content of 48.08% (Table 1). Using this reference transcriptome, 20,273 high quality SNPs were identified from 101 E. sibiricus accessions. Furthermore, the genome skimming data were used to assemble the E. sibiricus composite genome, which consisted of 33,234 contigs with a total length of more than 3.8 million bp, covering more than 0.05% of the 6.8 Gb nuclear genome. Among these contigs, 1525 had a length of more than 200 bp. A total of 72,344 SNPs were identified based on genome skimming data from 101 E. sibiricus accessions.

Table 1
www.frontiersin.org

Table 1. The quality assessment of the assembled reference transcriptome of E. sibiricus.

SNPs derived from the transcriptome data exhibited higher discriminatory ability for various geo-groups of E. sibiricus

The PCA plots and phylogenetic trees based on three data sets (transcriptome SNPs, the expression levels, and SNPs-GS) were combined to reveal the population structure of the tested E. sibiricus accessions (Figures 1, 2). In general, a greater discriminatory power of SNP data (both transcriptome SNPs and SNPs-GS) to discriminate different geo-groups was observed in PCA plots. Specifically, the PCA plot constructed using SNPs-GS could distinguish several E. sibiricus accessions from the QTP (Figure 1B), while the PCA plot constructed using transcriptome SNPs could distinguish more E. sibiricus accessions from the QTP and other regions (Figure 1C). However, based on expression levels, the tested E. sibiricus accessions had a mixed population structure (Figure 1A). In addition, the phylogenetic analysis also showed a greater discriminatory ability of transcriptome SNPs for distinguishing E. sibiricus accessions from different geo-groups (Figure 2), indicating the suitability of SNP data from transcriptome sequencing for further population structure analysis compared to expression levels or SNPs-GS.

Figure 1
www.frontiersin.org

Figure 1. The PCA plots based on the gene expression levels (A), SNPs called from the genome skimming [SNPs-GS, (B)] data, and transcriptome SNPs (C). QTP, Qinghai-Tibet Plateau, China; KAZA, Kazakhstan; MGL, Mongolia; NM, Inner Mongolia, China; RUSS, Russian; XJ, Xinjiang, China.

Figure 2
www.frontiersin.org

Figure 2. The hierarchical clustering based on Euclidean distance using the expression levels (A); Maximum likelihood tree using SNPs-GS (B) and transcriptome SNPs (C) of 101 E. sibiricus accessions.

Genetic diversity indices using transcriptome SNPs

As transcriptomic SNPs were more effective in revealing the population structure of E. sibiricus (Figures 1, 2), we subsequently used transcriptomic SNPs to perform further genetic studies. In summary, XJ and SC/XZ had the highest (0.3248) and lowest (0.3186) MAF values (Table 2), respectively. For O_het, except for the QH geo-group, all groups had values greater than 0.6, with the MGL geo-group having the highest value (0.625). However, the QH geo-group had the highest value of E_het (0.3894). The O_het values of all the geo-groups were greater than the E_het values.

Table 2
www.frontiersin.org

Table 2. Genetic diversity indices of each geo-group of E. sibiricus.

Gene flow and differentiation among geo-groups based on transcriptome SNPs

The result of the gene flow analysis showed that the optimal K value (migration edges) was eight, indicating the presence of eight gene flow events between the nine geo-groups of E. sibiricus (Supplementary Figure S1). This was consistent with the generally low Fst values between these geo-groups (Supplementary Figure S2). The SC geo-group had the highest number of gene flow events, including gene flows from QH and RUSS to SC, and SC to NM in the early stages (Figure 3). Only a single gene flow event was detected for the Canada, NM, KAZA, and XJ geo-groups. In contrast, no gene flow was observed between MGL and the remaining geo-groups.

Figure 3
www.frontiersin.org

Figure 3. The gene flow among nine geo-groups of E. sibiricus.

We further integrated the Pi values for each geo-group and the pairwise Fst values to identify the selected regions and associated genes. As the Canada geo-group contained only a single accession, it was excluded from this analysis. A total of 12, 267, 3, 81, 1, 54, 824, and 259 genes were identified in the XZ, XJ, SC, RUSS, QH, NM, MGL, and KAZA geo-groups, respectively. Three and one genes selected in the SC and QH geo-groups, respectively, could not be annotated in the GO database. The selected genes from all six geo-groups were involved in the “development” and “metabolic” processes (Figure 4). With the exception of the NM and KAZA geo-groups, the genes under selection in other geo-groups were also involved in the homeostasis process. In addition, the genes under selection in each geo-group showed responsiveness to specific stresses or stimuli, potentially contributing to the cumulative variation experienced during the long-term adaptation process to environmental factors.

Figure 4
www.frontiersin.org

Figure 4. The GO annotation result of genes under selection in each geo-group of E. sibiricus.

Population differentiation from the perspective of gene expression

Using the expression levels of all genes cannot effectively resolve the population structure of E. sibiricus (Figures 1A, 2A). Therefore, we attempted to analyze genes specifically expressed in each geo-group to investigate population differentiation from the standpoint of gene expression. A total of 414, 1899, 1797, 498, 1529, 3295, 556, and 4499 genes were specifically expressed in KAZA, MGL, NM, QH, RUSS, SC, XJ, and XZ geo-groups, respectively. The heatmap results indicated that the specifically expressed genes in each geo-group showed a significant difference in expression profiles (Supplementary Figure S3).

We also performed GSVA (gene set variation analysis) to identify differentially enriched gene sets in each geo-group compared to the others. Several GO terms related to plant energy metabolism processes were identified, including GO:0052855 and GO:0047453, which are associated with NAD(P)H-hydrate dehydratase activity and were significantly up-regulated in the KAZA geo-group. In addition, GO:0033178 (related to ATPase complex) and GO:0006086, GO:0006637, and GO:0047617 (related to acyl-CoA metabolic process), were significantly upregulated in the MGL geo-group. Furthermore, several GO terms related to carbohydrate metabolism pathways were discovered, including GO:0009052, GO:0061615, and GO:0003872 in the MGL geo-group, GO:0019673, and GO:0008446 in the RUSS geo-group, GO:0006486, GO:0008378, and GO:0019255 in the SC geo-group, GO:0004576 in the XJ geo-group, GO:0019375 and GO:0047714 in the XZ geo-group. Although the plants were grown under controlled growth conditions, some GO terms related to stress tolerance were also detected for some geo-groups. For example, GO:0009408 and GO:0031990, which are associated with heat stress, were up-regulated in the KAZA geo-group, GO:0010225 (response to UV-C) and GO:0009411 (response to UV) were down-regulated in the MGL and SC geo-groups, respectively. GO:1901700 (response to oxygen-containing compound) and GO:0071215 (cellular response to abscisic acid stimulus) were downregulated in the SC geo-group. In particular, six GO terms (GO:0006833, GO:0015793, GO:0015254, GO:0015250, GO:0009992, and GO:0016798) related to water transport were significantly downregulated in the XJ geo-group.

The PSEG were further analyzed between two geo-groups. The analysis revealed that the XZ geo-group had the highest number of shared specifically expressed genes shared with the other geo-group, with a total of 1599 genes (Figure 5). GO annotation results indicated that some of these genes were involved in the response process to UV (Figure 5). In addition, the common specifically expressed genes in the QH, NM and SC geo-groups were found to be responsive to ion, especially in the SC geo-group where the genes were responsive to salt and involved in ion transport process.

Figure 5
www.frontiersin.org

Figure 5. The Venn diagram of population-specifically-expressed genes between two geo-groups, and the GO annotation results of these shared specific-expressed-genes in each geo-group.

WGCNA analysis can help identify potential regulators of PSEG

In this study, we performed a weighted gene co-expression network analysis (WGCNA) to identify the possible core regulatory genes in PSEG. The result showed that all the co-expressed genes could be assigned to 46 modules (Supplementary Figure S4). The regulatory networks in each model identified by WGCNA analysis were constructed and an extensive regulatory relationship between TFs such as NAC, MYB, C2H2, and downstream genes was found in the black model (Figure 6A). Furthermore, we also identified the potential TFs that have the ability to regulate the expression of PSEG in each geo-group (Figure 6B). It is important to note that the genes in the QH, XJ, and NM geo-groups do not function as regulatory genes. Conversely, in the SC geo-group, we discovered two TFs (MADS-box and NAC) that play a regulatory role in the genes encoding the senescence-associated protease (SAG39) and the C2H2-finger domain. In addition, we identified more regulatory TFs in the XZ geo-group, including two genes belonging to the zinc finger family. Notably, our analysis also revealed that some PSEGs are regulated by multiple TFs. For example, one gene, DNA damage-repair/toleration (DRT), specifically expressed in the XZ geo-group, was regulated by six TFs. These findings highlight the importance of using transcriptome data to effectively identify potential population-specific regulatory genes that may be associated with their own local adaptation.

Figure 6
www.frontiersin.org

Figure 6. The node-link graph showing the regulating relationship between the population-specifically-expressed genes and the TFs. (A) regulatory network between TFs and genes in black model; (B) the node-link graph of PSEGs, the circles from the inside to out represent geo-groups, TFs and population-specific genes, respectively. The circle size indicates the number of times that the genes regulating or be regulated.

Discussion

To the best of our knowledge, this study represents the first attempt to assess the effectiveness of three methods - expression levels, transcriptome SNPs, and SNPs-GS - for analyzing population structure in a species lacking a reference genome, with a focus on E. sibiricus. The results showed that SNPs, especially transcriptome SNPs, were most effective in analyzing the population structure of E. sibiricus. This method identified numerous genes associated with local adaptation in E. sibiricus. In addition, although expression levels were less effective in population structure analysis, a significant number of PSEGs were also detected. Their annotations suggested their relevance to local environmental adaptation. Furthermore, by performing WGCNA analysis, some potential regulatory genes of the PSEGs were identified. Thus, we propose that in the absence of a reference genome, the use of transcriptome data (including both expression levels and SNP data) can reveal genes related to local adaptation and evolution of a species.

Transcriptome SNPs is an effective strategy in population analysis

SNP markers have several advantages over other markers, including ease of development and deployment. However, using SNP markers to study the population structure of certain species, particularly polyploidy species in the absence of reference genome information, can be challenging. Most previous studies have relied on genome skimming methods to obtain plastid sequences and nuclear ribosomal genes (Trevisan et al., 2019; Liu et al., 2021b). However, these approaches have only revealed limited genetic variation, which is insufficient for a comprehensive understanding of the true population structure (Del Valle et al., 2020). It is possible to jointly de novo assemble and identify evolutionarily informative sites from genome skimming data, as demonstrated for species identification in buffalo fish (Literman et al., 2023) and phylogenomic reconstruction in Leishmania (Harkins et al., 2016). Notably, there are no reports of genome skimming data being used to identify evolutionarily informative sites within species. Given the significant variation among the wild E. sibiricus accessions used in our study, we attempted to use genome skimming data to detect evolutionarily informative sites and analyze the population structure of E. sibiricus. The assembled composite genome covered approximately 0.05% of the E. sibiricus nuclear genome (Xiong et al., 2021). Although the coverage of typical simplified genome sequencing is typically around 5% (Literman et al., 2023), it remains a challenge to effectively assemble and align genome sequencing data, as well as complicating the annotation of variant sites, in the absence of the reference genome for population structure analysis. In addition, the PCA analysis distinguished only a few E. sibiricus accessions from Qinghai that showed significant differences from other accessions (Figure 1), while the phylogenetic tree results show that the accessions from the Qinghai-Tibetan Plateau (in purple) are generally clustered together, while the accessions from the Xinjiang are mainly clustered in three branches in the lower right corner (Figure 2). This suggests that in the absence of genome information, using genome skimming data to identify evolutionarily informative sites for population structure analysis is a viable alternative. However, it is essential to adequately increase the sequencing depth and propose more efficient algorithms for the analysis of short-read sequencing data to accurately infer genetic structure, especially for polyploid species with large genome sizes.

Data from coding genes allow for quality control steps that help to distinguish biological patterns from technical artefacts, enabling SNP analysis data to be tested against neutral expectations at multiple levels, outperforming typical outlier approaches (De Wit et al., 2015). Many researchers (Wang et al., 2021; Mossion et al., 2022) have successfully developed transcriptome SNPs for the analysis of population structure and genetic diversity. Furthermore, the power of transcriptome SNPs to study intraspecific relationships in Camellia sinensis has been shown to exceed that of low-copy nuclear genes (Cheng et al., 2023). In this study, the higher effectiveness of transcriptome SNPs in deciphering the population structure of E. sibiricus from different locations compared to expression levels and SNPs-GS (Figures 1, 2) was also found. On the other hand, transcriptomic SNPs may be concentrated in regions of active gene expression where variation and recombination may be more frequent, so the present study detected frequent gene flow (Figure 3) and generally small pairwise Fst coefficients between geo-groups using transcriptomic SNPs (Supplementary Figure S4). This is consistent with a previous research using chloroplast markers (Xiong et al., 2022). However, this seems to differ from the results of previous studies using whole chloroplast genomes (Xiong et al., 2023) and nuclear makers (Han et al., 2022): their results show that gene flow between geo-groups of E. sibiricus is relatively low due to the existence of geographic barriers. This may be because transcriptome SNPs capture more recent or small-scale gene flow than chloroplast or nuclear DNA, as these data provide more detailed genetic information (Chen et al., 2021; Tepolt and Palumbi, 2015).

The combination of transcriptome SNPs and expression levels can help understanding adaptive mechanism

Transcriptome SNP can reduce complexity and provide more accurate functional annotation than reduced representation of genomic DNA libraries. This is considered an important method for identifying genes associated with local adaptation for population genomic analyses in non-model plants (Cheng et al., 2023; Liu et al., 2021a). In this study, the Pi and pairwise Fst values based on transcriptome SNPs were used to identify genes under selection within each geo-group. The majority of these genes are involved in the regulation of homeostasis, growth, and developmental processes (Figure 4). While some genes under selection in each geo-group are involved in various stress processes, only the NM geo-group had genes annotated as responding to ion stress processes. This is noteworthy because the NM geo-group is an area with severe saline alkali soils, and E. sibiricus from this region shows stronger salt tolerance (Chen et al., 2023). However, no adaptive genes related to local climatic or environmental characteristics (such as the arid climate of Xinjiang and the high altitude of Tibet) were detected in other geo-groups, possibly due to the frequent gene flow events between E. sibiricus geo-groups (Figure 3).

In addition to transcriptome SNPs, variation in gene expression levels is also an important source of adaptive traits, as gene transcription levels serve as the medium for gene coding information and final phenotypes (Alonso-Blanco et al., 2009; Bullard et al., 2010). Previous studies have shown that gene expression levels do not support the expected population structure compared to transcriptome variation (Wang et al., 2018), which is consistent with the present study. However, to understand the impact of genetic variation in gene expression levels and its effect on trait adaptation, it is essential to characterize expression level variation at the population scale (Fraser et al., 2011). In this study, transcript abundance was determined at the individual level using 101 wild E. sibiricus accessions and PSEGs were identified. In the SC, QH, XZ, and NM geo-groups, the number of PSEGs exceeded the number of selective genes identified by transcriptomic SNPs, and more genes related to local climate adaptation were discovered, such as ion transport (caused by the severe saline-alkaline soils of SC, QH, and NM) and UV-B radiation (caused by the high altitude of XZ). As the expression levels of many genes controlling quantitative traits are often influenced by regulatory genes (i.e., TFs), this study used WGCNA analysis to explore some transcription factor family members, such as NAC and zinc finger protein, that could potentially regulate PSEGs. Identification of transcriptome SNPs and PSEGs associated with adaptation can shed light on the selective pressures faced by species in their natural environment and their effects on genotype and phenotype. The integration of genotype and regulatory network (especially functional network) is a prominent and inevitable trend in current research on adaptive evolution.

Materials and methods

Materials and transcriptome sequencing

A total of 101 accessions covering the main distribution regions of E. sibiricus were included in the present study, divided into seven geographical groups, namely MGL (Mongolia), RUSS (Russia), KAZA (Kazakhstan), Canada (Canada), XJ (Xinjiang, China), NM (Inner Mongolia, China), and QTP (Qinghai, China; Sichuan, China; and Xizang, China) (Supplementary Table S1). Accessions from MGL, RUSS, KAZA and Canada were collected from the National Plant Germplasm System (NPGS). The remaining accessions were collected by the research team according to the following rules: Spikelets were harvested from each individual plant, ensuring a minimum sampling distance of 50 meters between plants. Seeds of all accessions were planted in sand and grown in the greenhouse to minimize the influence of the environment on the expression of the different accessions. At the three-leaf stage, leaves from each accession were collected within one hour and immediately preserved in liquid nitrogen for subsequent RNA extraction. High quality RNA was purified and fragmented after assessment of purity, quantity, and RNA integrity. First-strand cDNA was then synthesized, followed by the addition of A-tailing and adaptor. The amplified products were then purified and paired‐end sequenced to a read length of 150 bp on the Illumina platform. Finally, approximately 6 Gb of raw data was obtained for each accession, with each accession having three biological replicates.

The assembly and annotation of the full-length transcriptome, and SNP calling

The full-length E. sibiricus transcriptome bam file was obtained from Yu et al. (2023) and converted to a fasta file using the bam2fasta tool (part of the bambamv1.4tool-kit) (Page et al., 2014). This was used for assembly using flye v2.9 with the following parameters: ‘flye –pacbio-raw input.fasta –out-dir out_pacbio’ (Kolmogorov et al., 2019), which uses repeat graphs for the assembly of long and error-prone reads. The quality of the assembly was accessed using QUAST (Gurevich et al., 2013). The resulting transcript sequences were aligned using the NR (Pruitt et al., 2005), COG (Tatusov et al., 2000), KOG (Koonin et al., 2004), KEGG (Kanehisa et al., 2004), and GO (Ashburner et al., 2000) databases with an E-value of 10-5. The transferred amino acid sequences were searched against the library of Pfam HMMs using pfam_scan.pl (Finn et al., 2014). Coding sequences (CDS) and transcription factors were then identified using the online software TransDecoder v3.0.0 (https://github.com/TransDecoder/TransDecoder) and ITAK v1.6 (Zheng et al., 2016), respectively.

Quality control was performed on the reads of the RNA sequencing data using the fastQC v0.12.0 software with the command ‘fastqc *.fastq.gz’ (https://www.bioinformatics.babraham.ac.uk/projects/fastqc/). Low quality sequences (Phred < 20 and length < 50 bp) and adaptor sequences were trimmed using trim_galore. The clean high-quality reads were compared to the full-length transcriptome data using RSEM v1.1.17 (Li and Dewey, 2011) to calculate gene abundance using default settings, which was further standardized to FPKM (fragment per kb per million reads).

Raw RNA sequencing data from one replicate of each accession were aligned to the assembled full-length transcriptome using the BWA-MEM algorithm of bwa v0.7.17-r1188 (Li, 2013; Tarasov et al., 2015) and converted to bam files using samtools v1.18 with the command ‘samtools view -b’ (Li et al., 2009), followed by the use of sambamba v0.5.9 (Li et al., 2009) to sort the resulting bam files and create index files using ‘sambamba index’. Finally, variant detection was performed using the HaplotypeCaller and GenotypeGVCFs with gatk v4.0 (McKenna et al., 2010). SNPs near indels were filtered, and the resulting vcf file was further filtered based on specific criteria: minor allele frequency (MAF) < 0.05, maximum missing data < 0.8, minimum depth of sequencing (minDP) < 2, maximum depth of sequencing (maxDP) < 1000, minimum Phred-scale quality score (minQ) < 30, minimum genotype quality score (minGQ) < 10. Finally, only biallelic loci are retained.

Genetic diversity and population structure analysis

SNPs obtained by mapping to the full-length transcriptome (transcriptome SNPs) were used to calculate MAF, observed heterozygosity (Ho), and expected heterozygosity (He) values for each geo-group using PLINK v1.90b4.6 software (Purcell et al., 2007). In addition, transcriptome SNPs were used to perform principal component analysis (PCA) using PLINK v1.90b4.6 (Purcell et al., 2007) with visualization using the pca_plink_plot R package. Expression levels were subjected to PCA analysis using the prcomp function and then visualized using the scatterplot3d R package (Mächler and Ligges, 2003). The vcf file was sorted using tassel v5.0 software (Bradbury et al., 2007) and then converted to Phylip format using run_pipeline.pl. This was then used to construct the maximum likelihood (ML) tree using FastTree v2.1 (Price et al., 2009). The hierarchical clustering tree was constructed based on the Euclidean distance using the ggraph R package (Si et al., 2020).

Using the vcf file containing all transcriptome variations, nucleotide diversity (Pi) values of each geo-group and pairwise genetic differentiation index (Fst) were calculated using vcftools v0.1.16 (Danecek et al., 2011) with a window size of 1000 bp and a step size of 100 bp. Regions with the top 5% Fst values were identified as candidate selected regions and used to extract genes under selection. Gene flow between geo-groups was analyzed using Treemix v1.13 software (Pickrell and Pritchard, 2012) and the optimal m value was accessed using the optM R package (Fitak, 2021). Finally, the plotting_funcs.R implemented in Treemix was used for visualization.

Population divergence in gene expression

The rsgcc R package (Ma and Wang, 2012) was used to identify PSEG with a threshold of 1. GSVA, a method for estimating variation in gene set enrichment through samples of an expression dataset, was used to determine the significantly different Gene Ontology (GO) terms between each geo-group and other accessions using the GSVA R package (Hänzelmann et al., 2013). Furthermore, the functional annotation of common specifically expressed genes in each geo-group was analyzed using the simplifyEnrichment R package (Gu and Hübschmann, 2023).

Homologous sequences isolation based on short read sequencing

SISRS (SNP Identification from Short Read Sequences) (Schwartz et al., 2015) allows the extraction of phylogenetically relevant sites from genome sequencing data, even for low coverage sequencing (genome skimming), and is not constrained by the availability of reference genome information. The genome skimming data for the test 101 E. sibiricus accessions were obtained from Xiong et al. (2023), with approximately 8 Gb of raw reads (fastq format) for each accession. Given that the genome size of E. sibiricus is approximately 6.86 Gb based on survey sequencing (Xiong et al., 2021), the data set of approximately 800 Gb can achieve a minimum coverage of approximately 10X and was found to be sufficient for assembly of a composite genome using Velvet v1.2.10 (Zerbino and Birney, 2008). The raw data for each accession were then mapped back to the composite genome using Bowtie 2 (Langmead and Salzberg, 2012) to extract conserved and variant regions. Alignment file containing the variant information were used to perform the PCA analysis and construct the ML trees using the adegenet (Jombart, 2008) and ggtree (Yu et al., 2017) R packages, respectively.

WGCNA analysis and network construction

WGCNA is a systems biology approach to describe the correlation patterns between genes (Langfelder and Horvath, 2008). We performed WGCNA using the WGCNA R package (Langfelder and Horvath, 2008) based on the gene expression matrix of all 101 accessions. The genes with the FPKM values greater than 0.1 in more than 95% of the samples were used for analysis (Li et al., 2020). The weighted score threshold was set to 0.8 (Wan et al., 2018; Liang et al., 2020), and then the regulatory network between transcription factor (TFs) genes and downstream genes was constructed and visualized using the ggraph R package (Si et al., 2020). The node-link graph of PSEGs was connected to show the unique regulatory network of each geo-group.

Data availability statement

The data presented in the study are deposited in the China National GeneBank DataBase repository (https://db.cngb.org/), accession number CNP0005048.

Author contributions

YLX: Writing – original draft, Methodology, Formal analysis, Data curation, Writing – review & editing. DL: Supervision, Conceptualization, Writing – review & editing, Writing – original draft. TL: Writing – original draft, Formal analysis, Writing – review & editing. YX: Writing – review & editing, Software, Data curation, Writing – original draft, Formal analysis. QY: Writing – review & editing, Supervision, Resources, Writing – original draft. XL: Writing – original draft, Methodology, Writing – review & editing. JZ: Writing – original draft, Software, Resources, Writing – review & editing. LY: Methodology, Writing – original draft, Writing – review & editing, Investigation. XM: Writing – original draft, Supervision, Funding acquisition, Writing – review & editing.

Funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. We thank the foundation of National Natural Science Foundation of China (32271753), Sichuan Province regional innovation cooperation project (2022TFQ0076), Key R & D project of Sichuan Province (2023YFN0087), and Cooperation project of provincial college, and provincial school (2023YFSY0012).

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Publisher’s note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Supplementary material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fpls.2024.1457980/full#supplementary-material

References

Alonso-Blanco, C., Aarts, M. G. M., Bentsink, L., Keurentjes, J. J. B., Reymond, M., Vreugdenhil, D., et al. (2009). What has natural variation taught us about plant development, physiology, and adaptation? Plant Cell 21, 1877–1896. doi: 10.1105/tpc.109.068114

PubMed Abstract | Crossref Full Text | Google Scholar

Ashburner, M., Ball, C. A., Blake, J. A., Botstein, D., Butler, H., Cherry, J. M., et al. (2000). Gene ontology: tool for the unification of biology. Nat. Genet. 25, 25–29. doi: 10.1038/75556

PubMed Abstract | Crossref Full Text | Google Scholar

Bradbury, P. J., Zhang, Z. W., Kroon, D. E., Casstevens, T. M., Ramdoss, Y., Buckler, E. S. (2007). TASSEL: software for association mapping of complex traits in diverse samples. Bioinformatics 23, 2633–2635. doi: 10.1093/bioinformatics/btm308

PubMed Abstract | Crossref Full Text | Google Scholar

Bullard, J. H., Mostovoy, Y., Dudoit, S., Brem, R. B. (2010). Polygenic and directional regulatory evolution across pathways in Saccharomyces. PNAS 107, 5058–5063. doi: 10.1073/pnas.0912959107

PubMed Abstract | Crossref Full Text | Google Scholar

Chen, C. L., Yang, W. J., Liu, J. Q., Xi, Z. X., Zhang, L., Hu, Q. (2021). Population transcriptomics reveals gene flow and introgression between two non-sister alpine gentians. Front. Ecol. Evolution 9. doi: 10.3389/fevo.2021.638230

Crossref Full Text | Google Scholar

Chen, S. M., Feng, J. J., Xiong, Y., Xiong, Y. L., Liu, Y. J., Zhao, J. M., et al. (2023). Evaluation and screening of wild Elymus sibiricus L. germplasm resources under salt stress. Agronomy 13, 2675. doi: 10.3390/agronomy13112675

Crossref Full Text | Google Scholar

Cheng, L., Li, M. G., Wang, Y. C., Han, Q. W., Hao, Y. L., Qiao, Z., et al. (2023). Transcriptome-based variations effectively untangling the intraspecific relationships and selection signals in Xinnyang Maojian tea population. Front. Plant Sci. 14. doi: 10.3389/fpls.2023.1114284

Crossref Full Text | Google Scholar

Danecek, P., Auton, A., Abecasis, G., Albers, C. A., Banks, E., DePristo, M. A., et al. (2011). The variant call format and vcftools. Bioinformatics 27, 2156–2158. doi: 10.1093/bioinformatics/btr330

PubMed Abstract | Crossref Full Text | Google Scholar

Del Valle, J. C., Herman, J. A., Whittall, J. B. (2020). Genome skimming and microsatellite analysis reveal contrasting patterns of genetic diversity in a rare sandhill endemic (Erysimum teretifolium, Brassicaceae). PloS One 15, e0227523. doi: 10.1371/journal.pone.0227523

PubMed Abstract | Crossref Full Text | Google Scholar

De Wit, P., Pespeni, M. H., Palumbi, S. R. (2015). SNP genotyping and population genomics from expressed sequences–current advances and future possibilities. Mol. Ecol. 24, 2310–2323. doi: 10.1111/mec.13165

PubMed Abstract | Crossref Full Text | Google Scholar

Finn, R. D., Bateman, A., Clements, J., Coggill, P., Eberhardt, R. Y., Eddy, S. R., et al. (2014). Pfam: the protein families database. Nucleic Acids Res. 42, 222–230. doi: 10.1093/nar/gkt1223

Crossref Full Text | Google Scholar

Fitak, R. R. (2021). OptM: estimating the optimal number of migration edges on population trees using Treemix. Biol. Methods Protoc. 6, bpab017. doi: 10.1093/biomethods/bpab017

PubMed Abstract | Crossref Full Text | Google Scholar

Fraser, H. B., Babak, T., Tsang, J., Zhou, Y. Q., Zhang, B., Mehrabian, M., et al. (2011). Systematic detection of polygenic cis-regulatory evolution. PloS Genet. 7, e1002023. doi: 10.1371/journal.pgen.1002023

PubMed Abstract | Crossref Full Text | Google Scholar

Gu, Z., Hübschmann, D. (2023). simplifyEnrichment: a Bioconductor package for clustering and visualizing functional enrichment results. Genomics Proteomics Bioinf. 21, 190–202. doi: 10.1016/j.gpb.2022.04.008

Crossref Full Text | Google Scholar

Gurevich, A., Saveliev, V., Vyahhi, N., Tesler, G. (2013). QUAST: quality assessment tool for genome assemblies. Bioinformatics 29, 107–115. doi: 10.1093/bioinformatics/btt086

Crossref Full Text | Google Scholar

Han, M. L., Zhang, J. X., Li, D. X., Sun, S. N., Zhang, C. B., Zhang, C. J., et al. (2022). Phylogeographical pattern and population evolution history of indigenous Elymus sibiricus L. @ on Qinghai-Tibetan Plateau. Front. Plant Sci. 13. doi: 10.3389/fpls.2022.882601

Crossref Full Text | Google Scholar

Hänzelmann, S., Castelo, R., Guinney, J. (2013). GSVA: gene set variation analysis for microarray and RNA-seq data. BMC Bioinf. 14, 1–15. doi: 10.1186/1471-2105-14-7

Crossref Full Text | Google Scholar

Harkins, K. M., Schwartz, R. S., Cartwright, R. A., Stone, A. C. (2016). Phylogenomic reconstruction supports supercontinent origins for leishmania. Infect. Genet. Evol. 38, 101–109. doi: 10.1016/j.meegid.2015.11.030

PubMed Abstract | Crossref Full Text | Google Scholar

Jombart, T. (2008). adegenet: a R package for the multivariate analysis of genetic markers. Bioinformatics 24, 1403–1405. doi: 10.1093/bioinformatics/btn129

PubMed Abstract | Crossref Full Text | Google Scholar

Kanehisa, M., Goto, S., Kawashima, S., Okuno, Y., Hattori, M. (2004). The KEGG resource for deciphering the genome. Nucleic Acids Res. 32, 277–280. doi: 10.1093/nar/gkh063

Crossref Full Text | Google Scholar

Kawecki, T. J., Ebert, D. (2004). Conceptual issues in local adaptation. Ecol. Lett. 7, 1225–1241. doi: 10.1111/j.1461-0248.2004.00684.x

Crossref Full Text | Google Scholar

Kolmogorov, M., Yuan, J., Lin, Y., Pevzner, P. A. (2019). Assembly of long, error-prone reads using repeat graphs. Nat. Biotechnol. 37, 540–546. doi: 10.1038/s41587-019-0072-8

PubMed Abstract | Crossref Full Text | Google Scholar

Koonin, E. V., Fedorova, N. D., Jackson, J. D., Jacobs, A. R., Krylov, D. M., Makarova, K. S., et al. (2004). A comprehensive evolutionary classification of proteins encoded in complete eukaryotic genomes. Genome Biol. 5, 1–28. doi: 10.1186/gb-2004-5-2-r7

Crossref Full Text | Google Scholar

Langfelder, P., Horvath, S. (2008). WGCNA: an r package for weighted correlation network analysis. BMC Bioinf. 9, 559–571. doi: 10.1186/1471-2105-9-559

Crossref Full Text | Google Scholar

Langmead, B., Salzberg, S. L. (2012). Fast gapped-read alignment with Bowtie 2. Nat. Methods 9, 357–359. doi: 10.1038/nmeth.1923

PubMed Abstract | Crossref Full Text | Google Scholar

Lei, Y. T., Zhao, Y. Y., Yu, F., Li, Y., Dou, Q. W. (2014). Development and characterization of 53 polymorphic genomic-SSR markers in Siberian wildrye (Elymus sibiricus L.). Conserv. Genet. Resour. 6, 861–864. doi: 10.1007/s12686-014-0225-5

Crossref Full Text | Google Scholar

Li, H. (2013). Aligning sequence reads, clone sequences and assembly contigs with BWA-MEM. arxiv preprint arxiv:1303.3997. doi: 10.48550/arXiv.1303.3997

Crossref Full Text | Google Scholar

Li, B., Dewey, C. N. (2011). RSEM: accurate transcript quantification from RNA-Seq data with or without a reference genome. BMC Bioinf. 12, 1–16. doi: 10.1186/1471-2105-12-323

Crossref Full Text | Google Scholar

Li, H., Handsaker, B., Wysoker, A., Fennell, T., Ruan, J., Homer, N., et al. (2009). The sequence alignment/map format and SAMtools. Bioinformatics 25, 2078–2079. doi: 10.1093/bioinformatics/btp352

PubMed Abstract | Crossref Full Text | Google Scholar

Li, Z. H., Wang, P. C., You, C. Y., Yu, J. W., Zhang, X. N., Yan, F. L., et al. (2020). Combined GWAS and eQTL analysis uncovers a genetic regulatory network orchestrating the initiation of secondary cell wall development in cotton. New Phytol. 226, 1738–1752. doi: 10.1111/nph.16468

PubMed Abstract | Crossref Full Text | Google Scholar

Liang, W., Sun, F., Zhao, Y., Shan, L., Lou, H. (2020). Identification of susceptibility modules and genes for cardiovascular disease in diabetic patients using WGCNA analysis. J. Diabetes Res. 2020, 4178639. doi: 10.1155/2020/4178639

PubMed Abstract | Crossref Full Text | Google Scholar

Limborg, M. T., Helyar, S. J., De Bruyn, M., Taylor, M. I., Nielsen, E. E., Ogden, R., et al. (2012). Environmental selection on transcriptome-derived SNPs in a high gene flow marine fish, the Atlantic herring (Clupea harengus). Mol. Ecol. 21, 3686–3703. doi: 10.1111/j.1365-294X.2012.05639.x

PubMed Abstract | Crossref Full Text | Google Scholar

Literman, R., Windsor, A. M., Bart, H. L., Jr., Hunter, E. S., Deeds, J. R., Handy, S. M. (2023). Using low-coverage whole genome sequencing (genome skimming) to delineate three introgressed species of buffalofish (Ictiobus). Mol. Phylogenet Evol. 182, 107715. doi: 10.1016/j.ympev.2023.107715

PubMed Abstract | Crossref Full Text | Google Scholar

Liu, B. B., Ma, Z. Y., Ren, C., Hodel, R. G., Sun, M., Liu, X. Q., et al. (2021b). Capturing single-copy nuclear genes, organellar genomes, and nuclear ribosomal DNA from deep genome skimming data for plant phylogenetics: A case study in Vitaceae. J. Systematics Evolution 59, 1124–1138. doi: 10.1111/jse.12806

Crossref Full Text | Google Scholar

Liu, L., Wang, Z., Su, Y. J., Wang, T. (2021a). Population transcriptomic sequencing reveals allopatric divergence and local adaptation in Pseudotaxus chienii (Taxaceae). BMC Genomics 22, 388. doi: 10.1186/s12864-021-07682-3

PubMed Abstract | Crossref Full Text | Google Scholar

López-Goldar, X., Agrawal, A. A. (2021). Ecological interactions, environmental gradients, and gene flow in local adaptation. Trends Plant Sci. 26, 796–809. doi: 10.1016/j.tplants.2021.03.006

PubMed Abstract | Crossref Full Text | Google Scholar

Ma, C., Wang, X. (2012). Application of the Gini correlation coefficient to infer regulatory relationships in transcriptome analysis. Plant Physiol. 160, 192–203. doi: 10.1104/pp.112.201962

PubMed Abstract | Crossref Full Text | Google Scholar

Mächler, M., Ligges, U. (2003). scatterplot3d - An R package for visualizing multivariate data. J. Stat. Software 8, 1–20. Available at: https://hdl.handle.net/10419/77160.

Google Scholar

McKenna, A., Hanna, M., Banks, E., Sivachenko, A., Cibulskis, K., Kernytsky, A., et al. (2010). The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. Genome Res. 20, 1297–1303. doi: 10.1101/gr.107524.110

PubMed Abstract | Crossref Full Text | Google Scholar

Mossion, V., Dauphin, B., Grant, J., Kessler, M., Zemp, N., Croll, D. (2022). Transcriptome-wide snps for botrychium lunaria ferns enable fine-grained analysis of ploidy and population structure. Mol. Ecol. Resour. 22, 254–271. doi: 10.1111/1755-0998.13478

PubMed Abstract | Crossref Full Text | Google Scholar

Page, J. T., Liechty, Z. S., Huynh, M. D., Udall, J. A. (2014). BamBam: genome sequence analysis tools for biologists. BMC Res. Notes 7, 1–5. doi: 10.1186/1756-0500-7-829

PubMed Abstract | Crossref Full Text | Google Scholar

Pickrell, J. K., Pritchard, J. K. (2012). Inference of population splits and mixtures from genome-wide allele frequency data. PLoS Genet 8 (11), e1002967. doi: 10.1371/journal.pgen.1002967

Crossref Full Text | Google Scholar

Pratlong, M., Haguenauer, A., Chabrol, O., Klopp, C., Pontarotti, P., Aurelle, D. (2015). The red coral (Corallium rubrum) transcriptome: a new resource for population genetics and local adaptation studies. Mol. Ecol. resources 15, 1205–1215. doi: 10.1111/1755-0998.12383

Crossref Full Text | Google Scholar

Price, M. N., Dehal, P. S., Arkin, A. P. (2009). FastTree: computing large minimum evolution trees with profiles instead of a distance matrix. Mol. Biol. Evol. 26, 1641–1650. doi: 10.1093/molbev/msp077

PubMed Abstract | Crossref Full Text | Google Scholar

Pruitt, K. D., Tatusova, T., Maglott, D. R. (2005). NCBI Reference Sequence (RefSeq): a curated non-redundant sequence database of genomes, transcripts and proteins. Nucleic Acids Res. 33, 501–504. doi: 10.1093/nar/gki025

Crossref Full Text | Google Scholar

Purcell, S., Neale, B., Todd-Brown, K., Thomas, L., Ferreira, M. A. R., Bender, D., et al. (2007). Plink: a tool set for whole-genome association and population-based linkage analyses. Am. J. Hum. Genet. 81, 559–575. doi: 10.1086/519795

PubMed Abstract | Crossref Full Text | Google Scholar

Richter, S., Schwarz, F., Hering, L., Böggemann, M., Bleidorn, C. (2015). The utility of genome skimming for phylogenomic analyses as demonstrated for glycerid relationships (Annelida, Glyceridae). Genome Biol. Evolution 7, 3443–3462. doi: 10.1093/gbe/evv224

Crossref Full Text | Google Scholar

Schwartz, R. S., Harkins, K. M., Stone, A. C., Cartwright, R. A. (2015). A composite genome approach to identify phylogenetically informative data from next-generation sequencing. BMC Bioinf. 16, 1–10. doi: 10.1186/s12859-015-0632-y

Crossref Full Text | Google Scholar

Schwinning, S., Lortie, C. J., Esque, T. C., DeFalco, L. A. (2022). What common-garden experiments tell us about climate responses in plants. J. Ecol. 110, 986–996. doi: 10.1111/1365-2745.13887

Crossref Full Text | Google Scholar

Shi, X. L., Ng, D. W. K., Zhang, C. Q., Comai, L., Ye, W. X., Chen, Z. J. (2012). Cis- and trans-regulatory divergence between progenitor species determines gene-expression novelty in arabidopsis allopolyploids. Nat. Commun. 3, 950. doi: 10.1038/ncomms1954

PubMed Abstract | Crossref Full Text | Google Scholar

Si, B. B., Liang, Y. X., Zhao, J., Zhang, Y., Liao, X. F., Jin, H., et al. (2020). GGraph: an efficient structure-aware approach for iterative graph processing. IEEE Trans. Big Data 8, 1182–1194. doi: 10.1109/TBDATA.2020.3019641

Crossref Full Text | Google Scholar

Signor, S. A., Nuzhdin, S. V. (2018). The evolution of gene expression in cis and trans. Trends Genet. 34, 532–544. doi: 10.1016/j.tig.2018.03.007

PubMed Abstract | Crossref Full Text | Google Scholar

Sun, C., Dong, Z., Zhao, L., Ren, Y., Zhang, N., Chen, F. (2020). The Wheat 660K SNP array demonstrates great potential for marker-assisted selection in polyploid wheat. Plant Biotechnol. J. 18, 1354–1360. doi: 10.1111/pbi.13361

PubMed Abstract | Crossref Full Text | Google Scholar

Tang, S., Zhao, H., Lu, S., Yu, L., Zhang, G., Zhang, Y., et al. (2021). Genome-and transcriptome-wide association studies provide insights into the genetic basis of natural variation of seed oil content in Brassica napus. Mol. Plant 14, 470–487. doi: 10.1016/j.molp.2020.12.003

PubMed Abstract | Crossref Full Text | Google Scholar

Tarasov, A., Vilella, A. J., Cuppen, E., Nijman, I. J., Prins, P. (2015). Sambamba: fast processing of NGS alignment formats. Bioinformatics 31, 2032–2034. doi: 10.1093/bioinformatics/btv098

PubMed Abstract | Crossref Full Text | Google Scholar

Tatusov, R. L., Galperin, M. Y., Natale, D. A., Koonin, E. V. (2000). The COG database: a tool for genome-scale analysis of protein functions and evolution. Nucleic Acids Res. 28, 33–36. doi: 10.1093/nar/28.1.33

PubMed Abstract | Crossref Full Text | Google Scholar

Tepolt, C. K., Palumbi, S. R. (2015). Transcriptome sequencing reveals both neutral and adaptive genome dynamics in a marine invader. Mol. Ecol. 24, 4145–4158. doi: 10.1111/mec.13294

PubMed Abstract | Crossref Full Text | Google Scholar

Thorstensen, M. J., Baerwald, M. R., Jeffries, K. M. (2021). RNA sequencing describes both population structure and plasticity-selection dynamics in a non-model fish. BMC Genomics 22, 1–12. doi: 10.1186/s12864-021-07592-4

PubMed Abstract | Crossref Full Text | Google Scholar

Thorstensen, M. J., Jeffrey, J. D., Treberg, J. R., Watkinson, D. A., Enders, E. C., Jeffries, K. M. (2020). Genomic signals found using RNA sequencing show signatures of selection and subtle population differentiation in walleye (Sander vitreus) in a large freshwater ecosystem. Ecol. Evolution 10, 7173–7188. doi: 10.1002/ece3.6418

Crossref Full Text | Google Scholar

Tiffin, P., Ross-Ibarra, J. (2014). Advances and limits of using population genetics to understand local adaptation. Trends Ecol. Evol. 29, 673–680. doi: 10.1016/j.tree.2014.10.004

PubMed Abstract | Crossref Full Text | Google Scholar

Trevisan, B., Alcantara, D. M., MaChado, D. J., Marques, F. P., Lahr, D. J. (2019). Genome skimming is a low-cost and robust strategy to assemble complete mitochondrial genomes from ethanol preserved specimens in biodiversity studies. PeerJ 7, e7543. doi: 10.7717/peerj.7543

PubMed Abstract | Crossref Full Text | Google Scholar

Wan, Q., Tang, J., Han, Y., Wang, D. (2018). Co-expression modules construction by WGCNA and identify potential prognostic markers of uveal melanoma. Exp. eye Res. 166, 13–20. doi: 10.1016/j.exer.2017.10.007

PubMed Abstract | Crossref Full Text | Google Scholar

Wang, C. Y., Liu, R., Liu., Y. J., Hou, W. W., Wang, X. J., Miao, Y. M., et al. (2021). Development and application of the Faba_bean_130K targeted next-generation sequencing SNP genotyping platform based on transcriptome sequencing. Theor. Appl. Genet. 134, 3195–3207. doi: 10.1007/s00122-021-03885-0

PubMed Abstract | Crossref Full Text | Google Scholar

Wang, W., Wang, H., Tang, H., Gan, J., Shi, C. G., Lu, Q., et al. (2018). Genetic structure of six cattle populations revealed by transcriptome-wide SNPs and gene expression. Genes Genomics 40, 715–724. doi: 10.1007/s13258-018-0677-1

PubMed Abstract | Crossref Full Text | Google Scholar

Xiong, Y., Lei, X., Bai, S. Q., Xiong, Y. L., Liu, W. H., Wu, W. D., et al. (2021). Genomic survey sequencing, development and characterization of single-and multi-locus genomic SSR markers of Elymus sibiricus L. BMC Plant Biol. 21, 1–12. doi: 10.1186/s12870-020-02770-0

PubMed Abstract | Crossref Full Text | Google Scholar

Xiong, Y., Xiong, Y. L., Jia, X. J., Zhao, J. M., Yan, L. J., Sha, L. N., et al. (2023). Divergence in Elymus sibiricus is related to geography and climate oscillation: a new look from pan-chloroplast genome data. J. Syst. Evol. 0, 1–15. doi: 10.1111/jse.13020

Crossref Full Text | Google Scholar

Xiong, Y., Xiong, Y. L., Shu, X., Yu, Q. Q., Lei, X., Li, D. X., et al. (2022). Molecular phylogeography and intraspecific divergences in siberian wildrye (Elymus sibiricus L.) wild populations in China, inferred from chloroplast DNA sequence and cpSSR markers. Front. Plant Sci. 13. doi: 10.3389/fpls.2022.862759

Crossref Full Text | Google Scholar

Yang, R. C. (1998). Estimating hierarchical F-statistics. Evolution 52, 950–956. doi: 10.1111/j.1558-5646.1998.tb01824.x

PubMed Abstract | Crossref Full Text | Google Scholar

Yu, G. C., Smith, D. K., Zhu, H. C., Guan, Y., Lam, T. T. Y. (2017). GGTREE: an R package for visualization and annotation of phylogenetic trees with their covariates and other associated data. Methods Ecol. Evol. 8, 28–36. doi: 10.1111/2041-210X.12628

Crossref Full Text | Google Scholar

Yu, Q. Q., Xiong, Y., Su, X. L., Xiong, Y. L., Dong, Z. X., Zhao, J. M., et al. (2023). Integrating full-length transcriptome and RNA sequencing of Siberian wildrye (Elymus sibiricus) to reveal molecular mechanisms in response to drought stress. Plants 12, 2719. doi: 10.3390/plants12142719

PubMed Abstract | Crossref Full Text | Google Scholar

Zerbino, D. R., Birney, E. (2008). Velvet: algorithms for de novo short read assembly using de Bruijn graphs. Genome Res. 18, 821–829. doi: 10.1101/gr.074492.107

PubMed Abstract | Crossref Full Text | Google Scholar

Zhang, X., Blaxter, M., Wood, J. M., Tracey, A., McCarthy, S., Thorpe, P., et al. (2024). Temporal genomics in Hawaiian crickets reveals compensatory intragenomic coadaptation during adaptive evolution. Nat. Commun. 15, 5001. doi: 10.1038/s41467-024-49344-4

PubMed Abstract | Crossref Full Text | Google Scholar

Zhang, Z. Y., Xie, W. W., Zhao, Y. Q., Zhang, J. C., Wang, N., Ntakirutimana, F., et al. (2019). EST-SSR marker development based on RNA-sequencing of E. sibiricus and its application for phylogenetic relationships analysis of seventeen Elymus species. BMC Plant Biol. 19, 1–18. doi: 10.1186/s12870-019-1825-8

PubMed Abstract | Crossref Full Text | Google Scholar

Zheng, Y., Jiao, C., Sun, H. H., Rosli, H. G., Pombo, M. A., Zhang, P. F., et al. (2016). iTAK: a program for genome-wide prediction and classification of plant transcription factors, transcriptional regulators, and protein kinases. Mol. Plant 9, 1667–1670. doi: 10.1016/j.molp.2016.09.014

PubMed Abstract | Crossref Full Text | Google Scholar

Zheng, Y. Y., Zhang, Z. Y., Wan, Y. Y., Tian, J. Y., Xie, W. G. (2020). Development of EST-SSR markers linked to flowering candidate genes in Elymus sibiricus L. based on RNA sequencing. Plants 9, 1371. doi: 10.3390/plants9101371

PubMed Abstract | Crossref Full Text | Google Scholar

Keywords: adaptability, transcriptome, genome skimming, SNPs, WGCNA, Elymus sibiricus

Citation: Xiong Y, Li D, Liu T, Xiong Y, Yu Q, Lei X, Zhao J, Yan L and Ma X (2024) Extensive transcriptome data providing great efficacy in genetic research and adaptive gene discovery: a case study of Elymus sibiricus L. (Poaceae, Triticeae). Front. Plant Sci. 15:1457980. doi: 10.3389/fpls.2024.1457980

Received: 01 July 2024; Accepted: 02 September 2024;
Published: 19 September 2024.

Edited by:

Michael L. Moody, The University of Texas at El Paso, United States

Reviewed by:

Michele Wyler, MWSchmid GmbH, Switzerland
Jingjing Wang, Jiangsu Province and Chinese Academy of Sciences, China

Copyright © 2024 Xiong, Li, Liu, Xiong, Yu, Lei, Zhao, Yan and Ma. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Lijun Yan, yanlijun456@126.com; Xiao Ma, maroar@126.com

These authors have contributed equally to this work

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.