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珍珠粟的表观遗传图谱揭示了CHH甲基化在调节组织特异性基因表达中的重要作用。

Epigenetic maps of pearl millet reveal a prominent role for CHH methylation in regulating tissue-specific gene expression.

作者信息

Luo Lin, Qu Qi, Cao Mengxue, Zhang Yihui, Sun Yuanchang, Mao Fei, Chen Jiaming, Zhu Yilin, Yang Yaorou, Li Chunxiao, Lin Dongmei, Lu Guodong, Lin Zhanxi, Zhu Fangjie, Xiao Jiajing

机构信息

College of Life Science, National Engineering Research Center of JUNCAO, Fujian Provincial Key Laboratory of Haixia Applied Plant Systems Biology, Haixia Institute of Science and Technology, Fujian Agriculture and Forestry University, Fuzhou, 350002 China.

Life Sciences Institute, Zhejiang University, Hangzhou, 310058 China.

出版信息

aBIOTECH. 2025 Aug 26;6(3):394-410. doi: 10.1007/s42994-025-00243-2. eCollection 2025 Sep.

Abstract

UNLABELLED

Pearl millet () is a major staple food in arid and semi-arid regions of sub-Saharan Africa, India, and South Asia. However, how epigenetic mechanisms regulate tissue-specific gene expression in this crop remains poorly understood. In this study, we profiled multiple epigenetic features in the young panicles and roots of pearl millet using RNA-seq, ATAC-seq, whole-genome bisulfite sequencing, and ChIP-seq (H3K4me3 and H3K36me3). We identified thousands of genes that were differentially expressed between these two tissues. Root-specific genes were enriched for plant hormone signaling, oxidative phosphorylation, and stress responses. Analysis of chromatin accessibility revealed that root-specific accessible chromatin regions (ACRs) were enriched in binding motifs for stress-responsive transcription factors (e.g., NAC, WRKY), whereas ACRs in young panicles were enriched in motifs for developmental regulators (e.g., AP2/ERF). DNA methylation profiling revealed 25,141 tissue-specific differentially methylated regions, with CHH methylation-rather than CG or CHG methylation-showing the strongest tissue specificity. Promoters of root-specific genes had higher levels of CHH methylation compared to those of young panicle-specific genes, suggesting that the roles of CHH methylation in regulating transcription might be tissue dependent. Notably, promoter-associated H3K4me3 marked panicle-specific genes, whereas root-specific expression was primarily linked to chromatin accessibility, suggesting a transcription factor-mediated regulatory mechanism. Together, our findings highlight the distinct epigenetic frameworks governing tissue-specific gene expression in pearl millet and provide valuable insights for advancing the genetic improvement of this crop.

SUPPLEMENTARY INFORMATION

The online version contains supplementary material available at 10.1007/s42994-025-00243-2.

摘要

未标注

珍珠粟()是撒哈拉以南非洲、印度和南亚干旱和半干旱地区的主要主食作物。然而,表观遗传机制如何调控该作物组织特异性基因表达仍知之甚少。在本研究中,我们利用RNA测序、ATAC测序、全基因组亚硫酸氢盐测序和ChIP测序(H3K4me3和H3K36me3)对珍珠粟幼穗和根中的多种表观遗传特征进行了分析。我们鉴定出数千个在这两个组织间差异表达的基因。根特异性基因在植物激素信号传导、氧化磷酸化和应激反应方面富集。对染色质可及性的分析表明,根特异性可及染色质区域(ACR)在应激反应转录因子(如NAC、WRKY)的结合基序中富集,而幼穗中的ACR在发育调节因子(如AP2/ERF)的基序中富集。DNA甲基化分析揭示了25141个组织特异性差异甲基化区域,其中CHH甲基化而非CG或CHG甲基化表现出最强的组织特异性。与幼穗特异性基因的启动子相比,根特异性基因的启动子具有更高水平的CHH甲基化,这表明CHH甲基化在转录调控中的作用可能依赖于组织。值得注意的是,启动子相关的H3K4me3标记了穗特异性基因,而根特异性表达主要与染色质可及性相关,这表明存在一种转录因子介导的调控机制。总之,我们的研究结果突出了控制珍珠粟组织特异性基因表达的独特表观遗传框架,并为推进该作物的遗传改良提供了有价值的见解。

补充信息

在线版本包含可在10.1007/s42994-025-00243-2获取的补充材料。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/82ed/12454808/6fb2b0ef7ff9/42994_2025_243_Fig1_HTML.jpg

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