以单核苷酸分辨率分析 207 个棉花品种的全种群 DNA 甲基化多态性,揭示表观基因组对复杂性状的贡献

IF 28.1 1区 生物学 Q1 CELL BIOLOGY Cell Research Pub Date : 2024-10-17 DOI:10.1038/s41422-024-01027-x
Ting Zhao, Xueying Guan, Yan Hu, Ziqian Zhang, Han Yang, Xiaowen Shi, Jin Han, Huan Mei, Luyao Wang, Lei Shao, Hongyu Wu, Qianqian Chen, Yongyan Zhao, Jiaying Pan, Yupeng Hao, Zeyu Dong, Xuan Long, Qian Deng, Shengjun Zhao, Mengke Zhang, Yumeng Zhu, Xiaowei Ma, Zequan Chen, Yayuan Deng, Zhanfeng Si, Xin Li, Tianzhen Zhang, Fei Gu, Xiaofeng Gu, Lei Fang
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引用次数: 0

摘要

DNA 甲基化在作物生长发育中起着多种调控作用。然而,甲基化多态性与天然作物种群中遗传多态性、基因表达和表型变异的关系在很大程度上仍然未知。在这里,我们调查了从 207 个棉花品种的花后 20 天(DPA)纤维中获得的高质量甲基组、转录组和基因组,并将群体遗传学的经典框架扩展到表观遗传学。研究发现了超过 2.87 亿个单甲基化多态性(SMPs),是单核苷酸多态性(SNPs)数量的 100 倍。这些单甲基化多态性在基因内区域明显富集,而在转座元件中却很少。关联分析进一步确定了共 5426782 个顺式甲基化数量性状位点(cis-meQTLs)、5078 个顺式表达数量性状甲基化位点(cis-eQTMs)和 9157 个表达数量性状位点(eQTLs)。值得注意的是,36.39% 的顺式-eQTM 基因与遗传变异无关,这表明与基因表达变异相关的大量 SMPs 与 SNPs 无关。此外,在与产量和纤维品质性状相关的 1715 个表观遗传位点中,只有 36 个(2.10%)与全基因组关联研究(GWAS)位点共享。多组学调控网络的构建揭示了 43 个可能参与纤维发育的顺式-逆式基因,而这些基因无法仅通过全基因组关联研究(GWAS)来确定。在这些基因中,有一个编码 CBL 交互蛋白激酶 10 的基因通过基因编辑成功验证了其在纤维长度调控中的作用。综上所述,我们的研究结果证明,DNA 甲基化数据可作为育种目的的额外资源,为加强和加快作物改良进程提供机会。
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Population-wide DNA methylation polymorphisms at single-nucleotide resolution in 207 cotton accessions reveal epigenomic contributions to complex traits

DNA methylation plays multiple regulatory roles in crop development. However, the relationships of methylation polymorphisms with genetic polymorphisms, gene expression, and phenotypic variation in natural crop populations remain largely unknown. Here, we surveyed high-quality methylomes, transcriptomes, and genomes obtained from the 20-days-post-anthesis (DPA) cotton fibers of 207 accessions and extended the classical framework of population genetics to epigenetics. Over 287 million single methylation polymorphisms (SMPs) were identified, 100 times more than the number of single nucleotide polymorphisms (SNPs). These SMPs were significantly enriched in intragenic regions while depleted in transposable elements. Association analysis further identified a total of 5,426,782 cis-methylation quantitative trait loci (cis-meQTLs), 5078 cis-expression quantitative trait methylation (cis-eQTMs), and 9157 expression quantitative trait loci (eQTLs). Notably, 36.39% of cis-eQTM genes were not associated with genetic variation, indicating that a large number of SMPs associated with gene expression variation are independent of SNPs. In addition, out of the 1715 epigenetic loci associated with yield and fiber quality traits, only 36 (2.10%) were shared with genome-wide association study (GWAS) loci. The construction of multi-omics regulatory networks revealed 43 cis-eQTM genes potentially involved in fiber development, which cannot be identified by GWAS alone. Among these genes, the role of one encoding CBL-interacting protein kinase 10 in fiber length regulation was successfully validated through gene editing. Taken together, our findings prove that DNA methylation data can serve as an additional resource for breeding purposes and can offer opportunities to enhance and expedite the crop improvement process.

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来源期刊
Cell Research
Cell Research 生物-细胞生物学
CiteScore
53.90
自引率
0.70%
发文量
2420
审稿时长
2.3 months
期刊介绍: Cell Research (CR) is an international journal published by Springer Nature in partnership with the Center for Excellence in Molecular Cell Science, Chinese Academy of Sciences (CAS). It focuses on publishing original research articles and reviews in various areas of life sciences, particularly those related to molecular and cell biology. The journal covers a broad range of topics including cell growth, differentiation, and apoptosis; signal transduction; stem cell biology and development; chromatin, epigenetics, and transcription; RNA biology; structural and molecular biology; cancer biology and metabolism; immunity and molecular pathogenesis; molecular and cellular neuroscience; plant molecular and cell biology; and omics, system biology, and synthetic biology. CR is recognized as China's best international journal in life sciences and is part of Springer Nature's prestigious family of Molecular Cell Biology journals.
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