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

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