MpTGA, together with MpNPR, regulates sexual reproduction and independently affects oil body formation in Marchantia polymorpha

Author:

Gutsche Nora1ORCID,Koczula Jens1ORCID,Trupp Melanie1ORCID,Holtmannspötter Michael2ORCID,Appelfeller Melanie1,Rupp Oliver3ORCID,Busch Andrea1ORCID,Zachgo Sabine1ORCID

Affiliation:

1. Division of Botany Osnabrück University 49076 Osnabrück Germany

2. Department of Biology and Center for Cellular Nanoanalytics (CellNanOs) Osnabrück University 49076 Osnabrück Germany

3. Bioinformatics and Systems Biology Justus Liebig University Giessen 35392 Giessen Germany

Abstract

Summary In angiosperms, basic leucine‐zipper (bZIP) TGACG‐motif‐binding (TGA) transcription factors (TFs) regulate developmental and stress‐related processes, the latter often involving NON EXPRESSOR OF PATHOGENESIS‐RELATED GENES (NPR) coregulator interactions. To gain insight into their functions in an early diverging land‐plant lineage, the single MpTGA and sole MpNPR genes were investigated in the liverwort Marchantia polymorpha. We generated Marchantia MpTGA and MpNPR knockout and overexpression mutants and conducted morphological, transcriptomic and expression studies. Furthermore, we investigated MpTGA interactions with wild‐type and mutagenized MpNPR and expanded our analyses including TGA TFs from two streptophyte algae. Mptga mutants fail to induce the switch from vegetative to reproductive development and lack gametangiophore formation. MpTGA and MpNPR proteins interact and Mpnpr mutant analysis reveals a novel coregulatory NPR role in sexual reproduction. Additionally, MpTGA acts independently of MpNPR as a repressor of oil body (OB) formation and can thereby affect herbivory. The single MpTGA TF exerts a dual role in sexual reproduction and OB formation in Marchantia. Common activities of MpTGA/MpNPR in sexual development suggest that coregulatory interactions were established after emergence of land‐plant‐specific NPR genes and contributed to the diversification of TGA TF functions during land‐plant evolution.

Funder

Bundesministerium für Bildung und Forschung

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