Time-course transcriptome analysis reveals gene co-expression networks and transposable element responses to cold stress in cotton.

IF 3.7 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY BMC Genomics Pub Date : 2025-03-12 DOI:10.1186/s12864-025-11433-z
Yan Dai, Jialiang Zhou, Baohong Zhang, Dewei Zheng, Kai Wang, Jinlei Han
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Abstract

Background: Cold stress significantly challenges cotton growth and productivity, yet the genetic and molecular mechanisms underlying cold tolerance remain poorly understood.

Results: We employed RNA-seq and iterative weighted gene co-expression network analysis (WGCNA) to investigate gene and transposable element (TE) expression changes at six cold stress time points (0 h, 2 h, 4 h, 6 h, 12 h, 24 h). Thousands of differentially expressed genes (DEGs) were identified, exhibiting time-specific patterns that highlight a phase-dependent transcriptional response. While the A and D subgenomes contributed comparably to DEG numbers, numerous homeologous gene pairs showed differential expression, indicating regulatory divergence. Iterative WGCNA uncovered 125 gene co-expression modules, with some enriched in specific chromosomes or chromosomal regions, suggesting localized regulatory hotspots for cold stress response. Notably, transcription factors, including MYB73, ERF017, MYB30, and OBP1, emerged as central regulators within these modules. Analysis of 11 plant hormone-related genes revealed dynamic expression, with ethylene (ETH) and cytokinins (CK) playing significant roles in stress-responsive pathways. Furthermore, we documented over 15,000 expressed TEs, with differentially expressed TEs forming five distinct clusters. TE families, such as LTR/Copia, demonstrated significant enrichment in these expression clusters, suggesting their potential role as modulators of gene expression under cold stress.

Conclusions: These findings provide valuable insights into the complex regulatory networks underlying cold stress response in cotton, highlighting key molecular components involved in cold stress regulation. This study provides potential genetic targets for breeding strategies aimed at enhancing cold tolerance in cotton.

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时间过程转录组分析揭示了棉花基因共表达网络和转座因子对冷胁迫的响应。
背景:冷胁迫显著影响棉花的生长和产量,但其耐寒性的遗传和分子机制尚不清楚。结果:我们采用RNA-seq和迭代加权基因共表达网络分析(WGCNA)来研究基因和转座元件(TE)在6个冷应激时间点(0小时、2小时、4小时、6小时、12小时和24小时)的表达变化。鉴定出数千个差异表达基因(deg),这些基因表现出时间特异性模式,突出了阶段依赖性转录反应。虽然A和D亚基因组对DEG数量的贡献相当,但许多同源基因对表现出差异表达,表明调控差异。迭代WGCNA发现了125个基因共表达模块,其中一些富集于特定的染色体或染色体区域,提示了冷胁迫响应的局部调控热点。值得注意的是,转录因子,包括MYB73、ERF017、MYB30和OBP1,在这些模块中成为中心调节因子。11个植物激素相关基因的动态表达分析显示,乙烯(ETH)和细胞分裂素(CK)在胁迫响应途径中发挥重要作用。此外,我们记录了超过15,000个表达的TEs,差异表达的TEs形成了五个不同的簇。TE家族,如LTR/Copia,在这些表达簇中表现出显著的富集,表明它们可能在冷胁迫下作为基因表达的调节剂。结论:这些发现为了解棉花冷胁迫反应的复杂调控网络提供了有价值的见解,突出了参与冷胁迫调控的关键分子成分。本研究为提高棉花耐寒性的育种策略提供了潜在的遗传靶点。
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来源期刊
BMC Genomics
BMC Genomics 生物-生物工程与应用微生物
CiteScore
7.40
自引率
4.50%
发文量
769
审稿时长
6.4 months
期刊介绍: BMC Genomics is an open access, peer-reviewed journal that considers articles on all aspects of genome-scale analysis, functional genomics, and proteomics. BMC Genomics is part of the BMC series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We offer an efficient, fair and friendly peer review service, and are committed to publishing all sound science, provided that there is some advance in knowledge presented by the work.
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