GmSPX5 regulates arbuscular mycorrhizal colonization and phosphate acquisition through modifying transcription profile and microbiome in soybean

IF 5.7 1区 生物学 Q1 PLANT SCIENCES
Xingqi Yang, Yuanyuan Li, Tianqi Wang, Zipei Li, Qingli Zhuang, Cuiyue Liang, Xiurong Wang, Jiang Tian
{"title":"GmSPX5 regulates arbuscular mycorrhizal colonization and phosphate acquisition through modifying transcription profile and microbiome in soybean","authors":"Xingqi Yang,&nbsp;Yuanyuan Li,&nbsp;Tianqi Wang,&nbsp;Zipei Li,&nbsp;Qingli Zhuang,&nbsp;Cuiyue Liang,&nbsp;Xiurong Wang,&nbsp;Jiang Tian","doi":"10.1111/tpj.70511","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>Symbiosis with arbuscular mycorrhizal (AM) fungi is a crucial strategy for plant adaptation to low phosphorus (P) stress. However, the mechanisms underlying how phosphate (Pi) signaling regulators participate in AM colonization remain largely unknown in soybean (<i>Glycine max</i>). In this study, the expression of <i>GmSPX5</i>, one member of the SPX (SYG1/Pho81/XPR1) family, was induced by AM fungal inoculation in soybean roots. Furthermore, the expression of <i>GmSPX5</i> seems to overlap with AM infection structures through analyzing GUS activity of transgenic soybean plants harboring <i>Pro<sub>GmSPX5</sub>:GUS</i>. Four transgenic lines with <i>GmSPX5</i> overexpression (OX8 and OX12) and suppression (Ri9 and Ri11) were subsequently used to examine the functions of <i>GmSPX5</i> on AM symbiosis and Pi acquisition. Despite no difference between Ri and wild-type (WT), the overexpression of <i>GmSPX5</i> significantly increased AM colonization as reflected by 8.4% in OX8 and 8.7% in OX12, respectively. Consistently, the dry weight and total P content of OX8 and OX12 were higher than WT. Furthermore, a total of 3483 genes were found to exhibit differential expression patterns in roots between OX12 and WT, including genes related to linolenic acid metabolism and flavonoid metabolism. Meanwhile, the composition of the bacterial community in the roots of OX12 was distinct from that in WT through β-diversity analysis. Particularly, an ASV19 (<i>Sphingomonadales</i>) was enriched in OX12 roots, which was positively related to total P content and AM fungi colonization. Taken together, these results highlight that <i>GmSPX5</i> can regulate AM symbiosis, as well as Pi acquisition in soybean. Our findings advance the understanding of SPX functions in plant–microbe interaction.</p>\n </div>","PeriodicalId":233,"journal":{"name":"The Plant Journal","volume":"124 1","pages":""},"PeriodicalIF":5.7000,"publicationDate":"2025-10-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Plant Journal","FirstCategoryId":"2","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/tpj.70511","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Symbiosis with arbuscular mycorrhizal (AM) fungi is a crucial strategy for plant adaptation to low phosphorus (P) stress. However, the mechanisms underlying how phosphate (Pi) signaling regulators participate in AM colonization remain largely unknown in soybean (Glycine max). In this study, the expression of GmSPX5, one member of the SPX (SYG1/Pho81/XPR1) family, was induced by AM fungal inoculation in soybean roots. Furthermore, the expression of GmSPX5 seems to overlap with AM infection structures through analyzing GUS activity of transgenic soybean plants harboring ProGmSPX5:GUS. Four transgenic lines with GmSPX5 overexpression (OX8 and OX12) and suppression (Ri9 and Ri11) were subsequently used to examine the functions of GmSPX5 on AM symbiosis and Pi acquisition. Despite no difference between Ri and wild-type (WT), the overexpression of GmSPX5 significantly increased AM colonization as reflected by 8.4% in OX8 and 8.7% in OX12, respectively. Consistently, the dry weight and total P content of OX8 and OX12 were higher than WT. Furthermore, a total of 3483 genes were found to exhibit differential expression patterns in roots between OX12 and WT, including genes related to linolenic acid metabolism and flavonoid metabolism. Meanwhile, the composition of the bacterial community in the roots of OX12 was distinct from that in WT through β-diversity analysis. Particularly, an ASV19 (Sphingomonadales) was enriched in OX12 roots, which was positively related to total P content and AM fungi colonization. Taken together, these results highlight that GmSPX5 can regulate AM symbiosis, as well as Pi acquisition in soybean. Our findings advance the understanding of SPX functions in plant–microbe interaction.

Abstract Image

GmSPX5通过调控转录谱和微生物组调控大豆丛枝菌根定植和磷酸盐获取。
与丛枝菌根(AM)真菌的共生是植物适应低磷胁迫的重要策略。然而,在大豆(Glycine max)中,磷酸(Pi)信号调节因子参与AM定植的机制仍然很大程度上未知。本研究通过AM真菌接种诱导大豆根系中SPX (SYG1/Pho81/XPR1)家族成员GmSPX5的表达。此外,通过分析携带ProGmSPX5:GUS的转基因大豆植株的GUS活性,GmSPX5的表达似乎与AM感染结构重叠。随后,利用GmSPX5过表达(OX8和OX12)和抑制(Ri9和Ri11)的4个转基因系,研究了GmSPX5对AM共生和Pi获取的作用。尽管Ri和野生型(WT)之间没有差异,但GmSPX5过表达显著增加了AM定植,在OX8和OX12中分别增加了8.4%和8.7%。同时,OX8和OX12的干重和总磷含量均高于WT。此外,共有3483个基因在OX12和WT的根中表现出差异表达模式,包括与亚麻酸代谢和类黄酮代谢相关的基因。同时,通过β-多样性分析,OX12根部的细菌群落组成与WT不同。其中,OX12根中富含ASV19 (Sphingomonadales),与总磷含量和AM真菌定植量呈正相关。综上所述,这些结果表明GmSPX5可以调节大豆AM的共生和Pi的获取。我们的发现促进了对SPX在植物与微生物相互作用中的功能的理解。
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 求助全文
来源期刊
The Plant Journal
The Plant Journal 生物-植物科学
CiteScore
13.10
自引率
4.20%
发文量
415
审稿时长
2.3 months
期刊介绍: Publishing the best original research papers in all key areas of modern plant biology from the world"s leading laboratories, The Plant Journal provides a dynamic forum for this ever growing international research community. Plant science research is now at the forefront of research in the biological sciences, with breakthroughs in our understanding of fundamental processes in plants matching those in other organisms. The impact of molecular genetics and the availability of model and crop species can be seen in all aspects of plant biology. For publication in The Plant Journal the research must provide a highly significant new contribution to our understanding of plants and be of general interest to the plant science community.
×
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
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
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 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信