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      A Putative Plasma Membrane Na +/H + Antiporter GmSOS1 Is Critical for Salt Stress Tolerance in Glycine max

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          Abstract

          Soybean ( Glycine max) is a staple crop and a major source of vegetable protein and vegetable oil. The growth of soybean is dramatically inhibited by salt stress, especially by the excessive toxic Na +. Salt Overly Sensitive 1 (SOS1) is the only extensively characterized Na + efflux transporter in multiple plant species so far. However, the role of GmSOS1 in soybean salt stress responses remains unclear. Herein, we created three gmsos1 mutants using the CRISPR-Cas9 system in soybean. We found a significant accumulation of Na + in the roots of the gmsos1 mutants, resulting in the imbalance of Na + and K +, which links to impaired Na + efflux and increased K + efflux in the roots of the gmsos1 mutants under salt stress. Compared to the wild type, our RNA-seq analysis revealed that the roots of the gmsos1-1 showed preferential up and downregulation of ion transporters under salt stress, supporting impaired stress detection or an inability to develop a comprehensive response to salinity in the gmsos1 mutants. Our findings indicate that the plasma membrane Na +/H + exchanger GmSOS1 plays a critical role in soybean salt tolerance by maintaining Na + homeostasis and provides evidence for molecular breeding to improve salt tolerance in soybean and other crops.

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          Most cited references60

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          MEGA X: Molecular Evolutionary Genetics Analysis across Computing Platforms.

          The Molecular Evolutionary Genetics Analysis (Mega) software implements many analytical methods and tools for phylogenomics and phylomedicine. Here, we report a transformation of Mega to enable cross-platform use on Microsoft Windows and Linux operating systems. Mega X does not require virtualization or emulation software and provides a uniform user experience across platforms. Mega X has additionally been upgraded to use multiple computing cores for many molecular evolutionary analyses. Mega X is available in two interfaces (graphical and command line) and can be downloaded from www.megasoftware.net free of charge.
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            Mechanisms of salinity tolerance.

            The physiological and molecular mechanisms of tolerance to osmotic and ionic components of salinity stress are reviewed at the cellular, organ, and whole-plant level. Plant growth responds to salinity in two phases: a rapid, osmotic phase that inhibits growth of young leaves, and a slower, ionic phase that accelerates senescence of mature leaves. Plant adaptations to salinity are of three distinct types: osmotic stress tolerance, Na(+) or Cl() exclusion, and the tolerance of tissue to accumulated Na(+) or Cl(). Our understanding of the role of the HKT gene family in Na(+) exclusion from leaves is increasing, as is the understanding of the molecular bases for many other transport processes at the cellular level. However, we have a limited molecular understanding of the overall control of Na(+) accumulation and of osmotic stress tolerance at the whole-plant level. Molecular genetics and functional genomics provide a new opportunity to synthesize molecular and physiological knowledge to improve the salinity tolerance of plants relevant to food production and environmental sustainability.
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              Salt and drought stress signal transduction in plants.

              Salt and drought stress signal transduction consists of ionic and osmotic homeostasis signaling pathways, detoxification (i.e., damage control and repair) response pathways, and pathways for growth regulation. The ionic aspect of salt stress is signaled via the SOS pathway where a calcium-responsive SOS3-SOS2 protein kinase complex controls the expression and activity of ion transporters such as SOS1. Osmotic stress activates several protein kinases including mitogen-activated kinases, which may mediate osmotic homeostasis and/or detoxification responses. A number of phospholipid systems are activated by osmotic stress, generating a diverse array of messenger molecules, some of which may function upstream of the osmotic stress-activated protein kinases. Abscisic acid biosynthesis is regulated by osmotic stress at multiple steps. Both ABA-dependent and -independent osmotic stress signaling first modify constitutively expressed transcription factors, leading to the expression of early response transcriptional activators, which then activate downstream stress tolerance effector genes.
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                Author and article information

                Contributors
                Journal
                Front Plant Sci
                Front Plant Sci
                Front. Plant Sci.
                Frontiers in Plant Science
                Frontiers Media S.A.
                1664-462X
                16 May 2022
                2022
                : 13
                : 870695
                Affiliations
                [1] 1Key Laboratory of Saline-Alkali Vegetation Ecology Restoration, Ministry of Education, College of Life Science, Northeast Forestry University , Harbin, China
                [2] 2State Key Laboratory of Tree Genetics and Breeding, Northeast Forestry University , Harbin, China
                [3] 3College of Life Science, Northeast Forestry University , Harbin, China
                [4] 4The Editorial Board of Journal of Forestry Research, Northeast Forestry University , Harbin, China
                [5] 5Laboratory Department, Qitaihe Center for Disease Control and Prevention , Qitaihe, China
                [6] 6Shanghai Center for Plant Stress Biology and Center for Excellence in Molecular Plant Sciences, Chinese Academy of Sciences , Shanghai, China
                [7] 7Department of Plant Science and Landscape Architecture, University of Maryland, College Park , College Park, MD, United States
                Author notes

                Edited by: Camilla Hill, Murdoch University, Australia

                Reviewed by: Hongwei Xun, Northeast Normal University, China; Min Zhu, Yangzhou University, China; Huatao Chen, Jiangsu Academy of Agricultural Sciences (JAAS), China; Igor Pottosin, University of Colima, Mexico

                *Correspondence: Jianhua Zhu, jhzhu@ 123456umd.edu

                These authors have contributed equally to this work

                This article was submitted to Plant Membrane Traffic and Transport, a section of the journal Frontiers in Plant Science

                Article
                10.3389/fpls.2022.870695
                9149370
                35651772
                49ecc2a3-f325-46d9-b43f-5d67fbb8f279
                Copyright © 2022 Zhang, Cao, Zhang, Xu, Yang, Li, Ji, Gao, Ali, Zhang, Zhu and Xie.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 14 February 2022
                : 29 March 2022
                Page count
                Figures: 5, Tables: 1, Equations: 0, References: 60, Pages: 14, Words: 10290
                Categories
                Plant Science
                Original Research

                Plant science & Botany
                gmsos1,soybean,na+ efflux,salt tolerance,breeding
                Plant science & Botany
                gmsos1, soybean, na+ efflux, salt tolerance, breeding

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