在小麦春化过程中,染色质环将上游调控因子聚集在一起进行有效的基因转录调控

IF 10.1 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Genome Biology Pub Date : 2024-12-03 DOI:10.1186/s13059-024-03437-x
Yanyan Liu, Xintong Xu, Chao He, Liujie Jin, Ziru Zhou, Jie Gao, Minrong Guo, Xin Wang, Chuanye Chen, Mohammed H. Ayaad, Xingwang Li, Wenhao Yan
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引用次数: 0

摘要

植物通过改变与染色质状态高度相关的基因转录来响应环境刺激,包括组蛋白修饰、染色质可及性和三维染色质相互作用。春化是冬小麦向生殖生长过渡的必要条件。小麦如何重塑其染色质特征,特别是在春化期间染色质相互作用,仍然未知。对不同春化条件下冬小麦的基因转录和组蛋白修饰进行组合分析,鉴定出17669个差异表达基因和H3K4me3、H3K27me3和H3K9ac的数千个差异富集峰。我们发现春化过程中的动态基因表达与H3K4me3高度相关。更重要的是,H3K4me3-和h3k9ac -相关的动态染色质相互作用表明春化导致染色质相互作用和基因激活增加。值得注意的是,VRN1和VRT2等主调控因子在空间上距离较远的靶点通过染色质环聚集在一起,实现高效的转录调控,这被称为“牧羊人”模式。此外,通过整合小麦春化与开花时间自然变异的基因调控网络,TaZNF10被鉴定为小麦春化相关开花时间的负调控因子。我们揭示了春化过程中的动态基因转录网络,发现空间上距离较远的基因可以通过与活性组蛋白标记相关的染色质环聚集在一起,从而更有效地被上游调节因子发现和结合。它为理解小麦和其他植物的春化和对环境刺激的反应提供了新的见解。
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Chromatin loops gather targets of upstream regulators together for efficient gene transcription regulation during vernalization in wheat
Plants respond to environmental stimuli by altering gene transcription that is highly related with chromatin status, including histone modification, chromatin accessibility, and three-dimensional chromatin interaction. Vernalization is essential for the transition to reproductive growth for winter wheat. How wheat reshapes its chromatin features, especially chromatin interaction during vernalization, remains unknown. Combinatory analysis of gene transcription and histone modifications in winter wheat under different vernalization conditions identifies 17,669 differential expressed genes and thousands of differentially enriched peaks of H3K4me3, H3K27me3, and H3K9ac. We find dynamic gene expression across the vernalization process is highly associated with H3K4me3. More importantly, the dynamic H3K4me3- and H3K9ac-associated chromatin-chromatin interactions demonstrate that vernalization leads to increased chromatin interactions and gene activation. Remarkably, spatially distant targets of master regulators like VRN1 and VRT2 are gathered together by chromatin loops to achieve efficient transcription regulation, which is designated as a “shepherd” model. Furthermore, by integrating gene regulatory network for vernalization and natural variation of flowering time, TaZNF10 is identified as a negative regulator for vernalization-related flowering time in wheat. We reveal dynamic gene transcription network during vernalization and find that the spatially distant genes can be recruited together via chromatin loops associated with active histone mark thus to be more efficiently found and bound by upstream regulator. It provides new insights into understanding vernalization and response to environmental stimuli in wheat and other plants.
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来源期刊
Genome Biology
Genome Biology Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
21.00
自引率
3.30%
发文量
241
审稿时长
2 months
期刊介绍: Genome Biology stands as a premier platform for exceptional research across all domains of biology and biomedicine, explored through a genomic and post-genomic lens. With an impressive impact factor of 12.3 (2022),* the journal secures its position as the 3rd-ranked research journal in the Genetics and Heredity category and the 2nd-ranked research journal in the Biotechnology and Applied Microbiology category by Thomson Reuters. Notably, Genome Biology holds the distinction of being the highest-ranked open-access journal in this category. Our dedicated team of highly trained in-house Editors collaborates closely with our esteemed Editorial Board of international experts, ensuring the journal remains on the forefront of scientific advances and community standards. Regular engagement with researchers at conferences and institute visits underscores our commitment to staying abreast of the latest developments in the field.
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