Strigolactone Biosynthesis in Medicago  truncatula and Rice Requires the Symbiotic GRAS-Type Transcription Factors NSP1 and NSP2

Author:

Liu Wei12,Kohlen Wouter3,Lillo Alessandra1,Op den Camp Rik1,Ivanov Sergey1,Hartog Marijke1,Limpens Erik1,Jamil Muhammad3,Smaczniak Cezary4,Kaufmann Kerstin4,Yang Wei-Cai2,Hooiveld Guido J.E.J.5,Charnikhova Tatsiana3,Bouwmeester Harro J.36,Bisseling Ton17,Geurts René1

Affiliation:

1. Department of Plant Science, Laboratory of Molecular Biology, Wageningen University, 6708 PB Wageningen, The Netherlands

2. Key Laboratory of Molecular and Developmental Biology, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China

3. Department of Plant Science, Laboratory of Plant Physiology, Wageningen University, 6708 PB Wageningen, The Netherlands

4. Plant Research International–Bioscience, Laboratory of Molecular Biology, 6708 PB Wageningen, The Netherlands

5. Division of Human Nutrition, Wageningen University, 6703 HD Wageningen, The Netherlands

6. Centre for BioSystems Genomics, 6708 PB Wageningen, The Netherlands

7. College of Science, King Saud University, Riyadh 11451, Saudi Arabia

Abstract

Abstract Legume GRAS (GAI, RGA, SCR)-type transcription factors NODULATION SIGNALING PATHWAY1 (NSP1) and NSP2 are essential for rhizobium Nod factor-induced nodulation. Both proteins are considered to be Nod factor response factors regulating gene expression after symbiotic signaling. However, legume NSP1 and NSP2 can be functionally replaced by nonlegume orthologs, including rice (Oryza sativa) NSP1 and NSP2, indicating that both proteins are functionally conserved in higher plants. Here, we show that NSP1 and NSP2 are indispensable for strigolactone (SL) biosynthesis in the legume Medicago truncatula and in rice. Mutant nsp1 plants do not produce SLs, whereas in M. truncatula, NSP2 is essential for conversion of orobanchol into didehydro-orobanchol, which is the main SL produced by this species. The disturbed SL biosynthesis in nsp1 nsp2 mutant backgrounds correlates with reduced expression of DWARF27, a gene essential for SL biosynthesis. Rice and M. truncatula represent distinct phylogenetic lineages that split approximately 150 million years ago. Therefore, we conclude that regulation of SL biosynthesis by NSP1 and NSP2 is an ancestral function conserved in higher plants. NSP1 and NSP2 are single-copy genes in legumes, which implies that both proteins fulfill dual regulatory functions to control downstream targets after rhizobium-induced signaling as well as SL biosynthesis in nonsymbiotic conditions.

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Plant Science

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