The serine–glycine–one-carbon metabolic network orchestrates changes in nitrogen and sulfur metabolism and shapes plant development

Author:

Rosa-Téllez Sara12ORCID,Alcántara-Enguídanos Andrea12ORCID,Martínez-Seidel Federico3ORCID,Casatejada-Anchel Ruben12ORCID,Saeheng Sompop4ORCID,Bailes Clayton L4ORCID,Erban Alexander3ORCID,Barbosa-Medeiros David3ORCID,Alepúz Paula15ORCID,Matus José Tomás6ORCID,Kopka Joachim3ORCID,Muñoz-Bertomeu Jesús2ORCID,Krueger Stephan7ORCID,Roje Sanja4ORCID,Fernie Alisdair R3ORCID,Ros Roc12ORCID

Affiliation:

1. Institut de Biotecnologia i Biomedicina (BIOTECMED), Universitat de València , 46100 Burjassot , Spain

2. Departament de Biologia Vegetal, Facultat de Farmàcia, Universitat de València , 46100 Burjassot , Spain

3. Max Planck Institute of Molecular Plant Physiology, 14476 Potsdam-Golm , Germany

4. Institute of Biological Chemistry, Washington State University , Pullman, WA 99164 , USA

5. Departament de Bioquímica y Biologia Molecular, Facultat de Biologia, Universitat de València , 46100 Burjassot , Spain

6. Institute for Integrative Systems Biology, I²SysBio, Universitat de València—CSIC , 46908 Paterna , Spain

7. Institute for Plant Sciences, University of Cologne , Zülpicherstraße 47b , 50674 Cologne, Germany

Abstract

Abstract L-serine (Ser) and L-glycine (Gly) are critically important for the overall functioning of primary metabolism. We investigated the interaction of the phosphorylated pathway of Ser biosynthesis (PPSB) with the photorespiration-associated glycolate pathway of Ser biosynthesis (GPSB) using Arabidopsis thaliana PPSB-deficient lines, GPSB-deficient mutants, and crosses of PPSB with GPSB mutants. PPSB-deficient lines mainly showed retarded primary root growth. Mutation of the photorespiratory enzyme Ser-hydroxymethyltransferase 1 (SHMT1) in a PPSB-deficient background resumed primary root growth and induced a change in the plant metabolic pattern between roots and shoots. Grafting experiments demonstrated that metabolic changes in shoots were responsible for the changes in double mutant development. PPSB disruption led to a reduction in nitrogen (N) and sulfur (S) contents in shoots and a general transcriptional response to nutrient deficiency. Disruption of SHMT1 boosted the Gly flux out of the photorespiratory cycle, which increased the levels of the one-carbon (1C) metabolite 5,10-methylene-tetrahydrofolate and S-adenosylmethionine. Furthermore, disrupting SHMT1 reverted the transcriptional response to N and S deprivation and increased N and S contents in shoots of PPSB-deficient lines. Our work provides genetic evidence of the biological relevance of the Ser–Gly–1C metabolic network in N and S metabolism and in interorgan metabolic homeostasis.

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Plant Science

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

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