Arabidopsis Topless‐related 1 mitigates physiological damage and growth penalties of induced immunity

Author:

Griebel Thomas12ORCID,Lapin Dmitry13ORCID,Locci Federica1ORCID,Kracher Barbara1,Bautor Jaqueline1,Concia Lorenzo4ORCID,Benhamed Moussa4ORCID,Parker Jane E.15ORCID

Affiliation:

1. Department of Plant–Microbe Interactions Max‐Planck Institute for Plant Breeding Research 50829 Cologne Germany

2. Dahlem Centre of Plant Sciences, Plant Physiology Freie Universität Berlin 14195 Berlin Germany

3. Translational Plant Biology, Department of Biology, Faculty of Science Utrecht University 3584 CH Utrecht the Netherlands

4. Institute of Plant Sciences Paris‐Saclay (IPS2), CNRS, INRA University Paris‐Sud, University of Evry, University Paris‐Diderot, Sorbonne Paris‐Cite, University of Paris‐Saclay Batiment 91405 Orsay France

5. Cluster of Excellence on Plant Sciences (CEPLAS) 40225 Düsseldorf Germany

Abstract

Summary Transcriptional corepressors of the Topless (TPL) family regulate plant hormone and immunity signaling. The lack of a genome‐wide profile of their chromatin associations limits understanding of the TPL family roles in transcriptional regulation. Chromatin immunoprecipitation with sequencing (ChIP‐Seq) was performed on Arabidopsis thaliana lines expressing GFP‐tagged Topless‐related 1 (TPR1‐GFP) with and without constitutive immunity via Enhanced Disease Susceptibility 1 (EDS1). RNA‐Seq profiling of the TPR1‐GFP lines and pathogen‐infected tpl/tpr mutants, combined with measuring immunity, growth, and physiological parameters was employed to investigate TPL/TPR roles in immunity and defense homeostasis. TPR1 was enriched at promoter regions of c. 1400 genes and c. 10% of the detected binding required EDS1 immunity signaling. In a tpr1 tpl tpr4 (t3) mutant, resistance to bacteria was slightly compromised, and defense‐related transcriptional reprogramming was weakly reduced or enhanced, respectively, at early (< 1 h) and late 24 h stages of bacterial infection. The t3 plants challenged with bacteria or pathogen‐associated molecular pattern nlp24 displayed photosystem II dysfunctions. Also, t3 plants were hypersensitive to phytocytokine pep1 at the level of root growth inhibition. Transgenic expression of TPR1 rescued these t3 physiological defects. We propose that TPR1 and TPL family proteins function in Arabidopsis to reduce detrimental effects associated with activated transcriptional immunity.

Funder

Deutsche Forschungsgemeinschaft

Publisher

Wiley

Subject

Plant Science,Physiology

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