Molecular cloning and characterization of a salt overly sensitive3 (SOS3) gene from the halophyte Pongamia.

IF 3.9 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Plant Molecular Biology Pub Date : 2024-05-14 DOI:10.1007/s11103-024-01459-4
Yi Zhang, Heng Yang, Yujuan Liu, Qiongzhao Hou, Shuguang Jian, Shulin Deng
{"title":"Molecular cloning and characterization of a salt overly sensitive3 (SOS3) gene from the halophyte Pongamia.","authors":"Yi Zhang, Heng Yang, Yujuan Liu, Qiongzhao Hou, Shuguang Jian, Shulin Deng","doi":"10.1007/s11103-024-01459-4","DOIUrl":null,"url":null,"abstract":"<p><p>A high concentration of sodium (Na<sup>+</sup>) is the primary stressor for plants in high salinity environments. The Salt Overly Sensitive (SOS) pathway is one of the best-studied signal transduction pathways, which confers plants the ability to export too much Na<sup>+</sup> out of the cells or translocate the cytoplasmic Na<sup>+</sup> into the vacuole. In this study, the Salt Overly Sensitive3 (MpSOS3) gene from Pongamia (Millettia pinnata Syn. Pongamia pinnata), a semi-mangrove, was isolated and characterized. The MpSOS3 protein has canonical EF-hand motifs conserved in other calcium-binding proteins and an N-myristoylation signature sequence. The MpSOS3 gene was significantly induced by salt stress, especially in Pongamia roots. Expression of the wild-type MpSOS3 but not the mutated nonmyristoylated MpSOS3-G2A could rescue the salt-hypersensitive phenotype of the Arabidopsis sos3-1 mutant, which suggested the N-myristoylation signature sequence of MpSOS3 was required for MpSOS3 function in plant salt tolerance. Heterologous expression of MpSOS3 in Arabidopsis accumulated less H<sub>2</sub>O<sub>2</sub>, superoxide anion radical (O<sub>2</sub><sup>-</sup>), and malondialdehyde (MDA) than wild-type plants, which enhanced the salt tolerance of transgenic Arabidopsis plants. Under salt stress, MpSOS3 transgenic plants accumulated a lower content of Na<sup>+</sup> and a higher content of K<sup>+</sup> than wild-type plants, which maintained a better K<sup>+</sup>/Na<sup>+</sup> ratio in transgenic plants. Moreover, no development and growth discrepancies were observed in the MpSOS3 heterologous overexpression plants compared to wild-type plants. Our results demonstrated that the MpSOS3 pathway confers a conservative salt-tolerant role and provided a foundation for further study of the SOS pathway in Pongamia.</p>","PeriodicalId":20064,"journal":{"name":"Plant Molecular Biology","volume":null,"pages":null},"PeriodicalIF":3.9000,"publicationDate":"2024-05-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Molecular Biology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1007/s11103-024-01459-4","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

A high concentration of sodium (Na+) is the primary stressor for plants in high salinity environments. The Salt Overly Sensitive (SOS) pathway is one of the best-studied signal transduction pathways, which confers plants the ability to export too much Na+ out of the cells or translocate the cytoplasmic Na+ into the vacuole. In this study, the Salt Overly Sensitive3 (MpSOS3) gene from Pongamia (Millettia pinnata Syn. Pongamia pinnata), a semi-mangrove, was isolated and characterized. The MpSOS3 protein has canonical EF-hand motifs conserved in other calcium-binding proteins and an N-myristoylation signature sequence. The MpSOS3 gene was significantly induced by salt stress, especially in Pongamia roots. Expression of the wild-type MpSOS3 but not the mutated nonmyristoylated MpSOS3-G2A could rescue the salt-hypersensitive phenotype of the Arabidopsis sos3-1 mutant, which suggested the N-myristoylation signature sequence of MpSOS3 was required for MpSOS3 function in plant salt tolerance. Heterologous expression of MpSOS3 in Arabidopsis accumulated less H2O2, superoxide anion radical (O2-), and malondialdehyde (MDA) than wild-type plants, which enhanced the salt tolerance of transgenic Arabidopsis plants. Under salt stress, MpSOS3 transgenic plants accumulated a lower content of Na+ and a higher content of K+ than wild-type plants, which maintained a better K+/Na+ ratio in transgenic plants. Moreover, no development and growth discrepancies were observed in the MpSOS3 heterologous overexpression plants compared to wild-type plants. Our results demonstrated that the MpSOS3 pathway confers a conservative salt-tolerant role and provided a foundation for further study of the SOS pathway in Pongamia.

Abstract Image

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
来自盐生植物 Pongamia 的盐过度敏感 3 (SOS3) 基因的分子克隆和特征描述。
高浓度钠(Na+)是植物在高盐度环境中面临的主要压力。盐过度敏感(SOS)通路是研究得最清楚的信号转导通路之一,它赋予植物将过多的 Na+ 从细胞中排出或将细胞质中的 Na+ 转移到液泡中的能力。本研究分离并鉴定了来自半红树 Pongamia(Millettia pinnata Syn. Pongamia pinnata)的盐过度敏感3(MpSOS3)基因。MpSOS3 蛋白具有与其他钙结合蛋白相同的典型 EF 手基序和 N-肉豆蔻酰化特征序列。盐胁迫会显著诱导 MpSOS3 基因,尤其是在芒果根中。表达野生型 MpSOS3 而非变异的非肉豆蔻酰化的 MpSOS3-G2A 能挽救拟南芥 sos3-1 突变体的盐敏感表型,这表明 MpSOS3 的 N-肉豆蔻酰化特征序列是 MpSOS3 在植物耐盐性中发挥作用的必要条件。异源表达MpSOS3的拟南芥比野生型植株积累更少的H2O2、超氧阴离子自由基(O2-)和丙二醛(MDA),这增强了转基因拟南芥植株的耐盐性。在盐胁迫下,与野生型植物相比,MpSOS3 转基因植物积累的 Na+ 含量较低,而 K+ 含量较高,这使转基因植物保持了较好的 K+/Na+ 比率。此外,与野生型植株相比,MpSOS3异源过表达植株的发育和生长没有出现差异。我们的研究结果表明,MpSOS3 途径具有保守的耐盐作用,为进一步研究 Pongamia 的 SOS 途径奠定了基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Plant Molecular Biology
Plant Molecular Biology 生物-生化与分子生物学
自引率
2.00%
发文量
95
审稿时长
1.4 months
期刊介绍: Plant Molecular Biology is an international journal dedicated to rapid publication of original research articles in all areas of plant biology.The Editorial Board welcomes full-length manuscripts that address important biological problems of broad interest, including research in comparative genomics, functional genomics, proteomics, bioinformatics, computational biology, biochemical and regulatory networks, and biotechnology. Because space in the journal is limited, however, preference is given to publication of results that provide significant new insights into biological problems and that advance the understanding of structure, function, mechanisms, or regulation. Authors must ensure that results are of high quality and that manuscripts are written for a broad plant science audience.
期刊最新文献
A new Bowman-Birk type protease inhibitor regulated by MeJA pathway in maize exhibits anti-feedant activity against the Ostrinia furnacalis. Highly divergent satellitomes of two barley species of agronomic importance, Hordeum chilense and H. vulgare. Improving organoleptic and antioxidant properties by inhibition of novel miRstv_7 to target key genes of steviol glycosides biosynthetic pathway in Stevia rebaudiana Bertoni. Low-dose 60Co-γ-ray irradiation promotes the growth of cucumber seedlings by inducing CsSAUR37 expression. Genome‑wide analysis of the GT8 gene family in apple and functional identification of MhGolS2 in saline-alkali tolerance.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1