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BZR1 转录因子通过番茄中 FERONIA 受体样激酶介导的活性氧信号转导调控耐热性。

BZR1 Transcription Factor Regulates Heat Stress Tolerance Through FERONIA Receptor-Like Kinase-Mediated Reactive Oxygen Species Signaling in Tomato.

机构信息

Department of Horticulture, Zijingang Campus, Zhejiang University, 866 Yuhangtang Road, Hangzhou, PR China.

School of Resources and Environmental Engineering, Ludong University, Yantai, PR China.

出版信息

Plant Cell Physiol. 2018 Nov 1;59(11):2239-2254. doi: 10.1093/pcp/pcy146.

DOI:10.1093/pcp/pcy146
PMID:30107607
Abstract

BRASSINAZOLE RESISTANT 1 (BZR1), the critical regulator of brassinosteroid (BR) response, participates in various BR-mediated developmental processes. However, the roles of BZR1 in stress tolerance are less clear. Here, we found that BZR1-like protein in tomato controls BR response and is involved in thermotolerance by regulating the FERONIA (FER) homologs. The CRISPR-bzr1 mutant showed reduced growth and was not responsive to 24-epibrassinolide (EBR) with regard to the promotion of plant growth. Mutation in BZR1 impaired the induction of RESPIRATORY BURST OXIDASE HOMOLOG1 (RBOH1), production of H2O2 in the apoplast and heat tolerance. Exogenous H2O2 recovered the heat tolerance of the tomato bzr1 mutant. Overexpression of BZR1 enhanced the production of apoplastic H2O2 and heat stress responses. However, silencing of RBOH1 abolished the BZR1-mediated heat tolerance. Further analysis showed that BZR1 bound to the promoters of FERONIA2 (FER2) and FER3 and induced their expression. Silencing of FER2/3 suppressed BZR1-dependent BR signaling for the induction of RBOH1 transcripts, accumulation of apoplastic H2O2 and heat tolerance. These results indicate that BZR1 regulates heat stress responses in tomato through RBOH1-dependent reactive oxygen species (ROS) signaling, which is at least partially mediated by FER2 and FER3.

摘要

BRASSINAZOLE RESISTANT 1 (BZR1),作为油菜素内酯 (BR) 响应的关键调控因子,参与了各种 BR 介导的发育过程。然而,BZR1 在胁迫耐受中的作用还不太清楚。在这里,我们发现番茄中的 BZR1 样蛋白通过调控 FERONIA (FER) 同源物来控制 BR 反应,并参与耐热性。CRISPR-bzr1 突变体表现出生长减缓,并且对 24-表油菜素内酯 (EBR) 的促进植物生长的反应降低。BZR1 的突变损害了 RESPIRATORY BURST OXIDASE HOMOLOG1 (RBOH1)的诱导、质外体中 H2O2 的产生和耐热性。外源性 H2O2 恢复了番茄 bzr1 突变体的耐热性。BZR1 的过表达增强了质外体 H2O2 的产生和热应激反应。然而,RBOH1 的沉默消除了 BZR1 介导的耐热性。进一步分析表明,BZR1 结合到 FERONIA2 (FER2) 和 FER3 的启动子上,并诱导它们的表达。FER2/3 的沉默抑制了 BZR1 依赖的 BR 信号转导,从而诱导 RBOH1 转录物、质外体 H2O2 的积累和耐热性。这些结果表明,BZR1 通过 RBOH1 依赖的活性氧 (ROS) 信号调节番茄的热应激反应,这至少部分是由 FER2 和 FER3 介导的。

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