HSFA1a modulates plant heat stress responses and alters the 3D chromatin organization of enhancer-promoter interactions

Author:

Huang YingORCID,An JingORCID,Sircar Sanchari,Bergis Clara,Lopes Chloé Dias,He Xiaoning,Da Costa Barbara,Tan Feng-Quan,Bazin Jeremie,Antunez-Sanchez JavierORCID,Mammarella Maria Florencia,Devani Ravi-sureshbhaiORCID,Brik-Chaouche Rim,Bendahmane Abdelhafid,Frugier Florian,Xia ChongjingORCID,Rothan Christophe,Probst Aline V.ORCID,Mohamed Zouine,Bergounioux Catherine,Delarue Marianne,Zhang YijingORCID,Zheng ShaojianORCID,Crespi Martin,Fragkostefanakis Sotirios,Mahfouz Magdy M.ORCID,Ariel Federico,Gutierrez-Marcos JoseORCID,Raynaud Cécile,Latrasse David,Benhamed MoussaORCID

Abstract

AbstractThe complex and dynamic three-dimensional organization of chromatin within the nucleus makes understanding the control of gene expression challenging, but also opens up possible ways to epigenetically modulate gene expression. Because plants are sessile, they evolved sophisticated ways to rapidly modulate gene expression in response to environmental stress, that are thought to be coordinated by changes in chromatin conformation to mediate specific cellular and physiological responses. However, to what extent and how stress induces dynamic changes in chromatin reorganization remains poorly understood. Here, we comprehensively investigated genome-wide chromatin changes associated with transcriptional reprogramming response to heat stress in tomato. Our data show that heat stress induces rapid changes in chromatin architecture, leading to the transient formation of promoter-enhancer contacts, likely driving the expression of heat-stress responsive genes. Furthermore, we demonstrate that chromatin spatial reorganization requires HSFA1a, a transcription factor (TF) essential for heat stress tolerance in tomato. In light of our findings, we propose that TFs play a key role in controlling dynamic transcriptional responses through 3D reconfiguration of promoter-enhancer contacts.

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry,Multidisciplinary

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3