PlWRKY47 Coordinates With Cytosolic Glyceraldehyde‐3‐Phosphate Dehydrogenase 2 Gene to Improve Thermotolerance Through Inhibiting Reactive Oxygen Species Generation in Herbaceous Peony

Author:

Zhao Daqiu1,Cheng Zhuoya1,Qian Yi1,Hu Ziao1,Tang Yuhan1,Huang Xingqi2,Tao Jun1ORCID

Affiliation:

1. College of Horticulture and Landscape Architecture Yangzhou University Yangzhou China

2. Department of Biochemistry Purdue University West Lafayette Indiana USA

Abstract

ABSTRACTAlthough WRKY transcription factors play crucial roles in plant responses to high‐temperature stress, little is known about Group IIb WRKY family members. Here, we identified the WRKY‐IIb protein PlWRKY47 from herbaceous peony (Paeonia lactiflora Pall.), which functioned as a nuclear‐localized transcriptional activator. The expression level of PlWRKY47 was positively correlated with high‐temperature tolerance. Silencing of PlWRKY47 in P. lactiflora resulted in the decreased tolerance to high‐temperature stress by accumulating reactive oxygen species (ROS). Overexpression of PlWRKY47 improved plant high‐temperature tolerance through decreasing ROS accumulation. Moreover, PlWRKY47 directly bound to the promoter of cytosolic glyceraldehyde‐3‐phosphate dehydrogenase 2 (PlGAPC2) gene and activated its transcription. PlGAPC2 was also positively regulated high‐temperature tolerance in P. lactiflora by increasing NAD+ content to inhibit ROS generation. Additionally, PlWRKY47 physically interacted with itself to form a homodimer, and PlWRKY47 could also interact with one Group IIb WRKY family member PlWRKY72 to form a heterodimer, they all promoted PlWRKY47 to bind to and activate PlGAPC2. These data support that the PlWRKY47‐PlWRKY47 homodimer and PlWRKY72‐PlWRKY47 heterodimer can directly activate PlGAPC2 expression to improve high‐temperature tolerance by inhibiting ROS generation in P. lactiflora. These results will provide important insights into the plant high‐temperature stress response by WRKY‐IIb transcription factors.

Publisher

Wiley

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