壶状菌的基本发育过程需要由功能冗余的PpROP GTPases提供不同水平的总活性。

IF 8.1 1区 生物学 Q1 PLANT SCIENCES
New Phytologist Pub Date : 2025-10-05 DOI:10.1111/nph.70603
Aude Le Bail,Benedikt Kost,Janina Nüssel,Tamara Isabeau Lolis,David Koch,Hildegard Voll,Sylwia Schulmeister,Alexander Kaier,Karin Ljung,Maria Ntefidou
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引用次数: 0

摘要

RHO (RAS同源)gtpase在大多数真核生物中调节重要的细胞和发育过程。植物特异性ROP(植物的RHO) GTPase家族在维管植物的进化过程中得到了扩展和功能多样化,但在早期陆地植物的非维管近缘中却很少有成员。本文系统地研究了PpROP在无维管束苔藓壶菌发育过程中的基本功能。这项研究的基础是:敲除四个PpROP基因中的每个基因的单独或所有可能的组合,这四个基因编码几乎相同的蛋白质;用野生型(WT)或突变的PpROPs或异源同源物补充敲除系;诱导PpROP过表达。PpROPs在细胞增殖、茎突分化和配子体形成中具有未知的功能。观察到PpROP功能对鸟苷二磷酸(GDP)/鸟苷三磷酸(GTP)循环表现出不同的依赖性,并依赖于不同的下游信号。不同的细胞和发育过程需要不同水平的总PpROP活性,而不是单个PpROPs。这些观察结果为PpROP在植物中的功能和信号传导提供了重要的见解,增强了我们对ROP/RHO GTPases调控发育过程的进化的理解。讨论了PpROP家族中显著的功能整合和序列保守的进化起源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Essential developmental processes in Physcomitrium patens require distinct levels of total activity provided by functionally redundant PpROP GTPases.
RHO (RAS homologous) GTPases regulate important cellular and developmental processes in most eukaryotes. Plant-specific ROP (RHO of plants) GTPase families expanded and functionally diversified during the evolution of vascular plants, but contain few members in nonvascular extant relatives of early land plants. Here, a systematic investigation of essential PpROP functions in the development of the nonvascular moss Physcomitrium patens is presented. This investigation was based on: knocking out individually or all possible combinations of each of the four PpROP genes, which encode nearly identical proteins; complementing knockout lines with wild-type (WT) or mutated PpROPs, or with heterologous homologs; and inducing PpROP overexpression. PpROPs were found to have previously unknown functions in cell proliferation, caulonema differentiation, and gametophore formation. PpROP functions were observed to display variable dependence on guanosine diphosphate (GDP)/guanosine triphosphate (GTP) cycling and to rely on distinct downstream signaling. Different cellular and developmental processes were determined to require distinct levels of total PpROP activity, rather than individual PpROPs. These observations provide important insights into PpROP functions and signaling in P. patens, enhancing our understanding of the evolution of the regulation of developmental processes by ROP/RHO GTPases. The evolutionary origin of the remarkable functional integration and sequence conservation within the PpROP family is discussed.
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来源期刊
New Phytologist
New Phytologist 生物-植物科学
自引率
5.30%
发文量
728
期刊介绍: New Phytologist is an international electronic journal published 24 times a year. It is owned by the New Phytologist Foundation, a non-profit-making charitable organization dedicated to promoting plant science. The journal publishes excellent, novel, rigorous, and timely research and scholarship in plant science and its applications. The articles cover topics in five sections: Physiology & Development, Environment, Interaction, Evolution, and Transformative Plant Biotechnology. These sections encompass intracellular processes, global environmental change, and encourage cross-disciplinary approaches. The journal recognizes the use of techniques from molecular and cell biology, functional genomics, modeling, and system-based approaches in plant science. Abstracting and Indexing Information for New Phytologist includes Academic Search, AgBiotech News & Information, Agroforestry Abstracts, Biochemistry & Biophysics Citation Index, Botanical Pesticides, CAB Abstracts®, Environment Index, Global Health, and Plant Breeding Abstracts, and others.
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