Symbiosomal Proteomic Analysis Reveals the Implication of Endosomal Regulators and CAPs in the Formation of Peanut Nodules.

IF 5.4 2区 生物学 Q1 PLANT SCIENCES
Zhao Zheng, Wenjing Ke, Chuanliang Liu, Haomin Cai, Danting Zhu, Qingren Liu, Chuhan Ji, Lei Feng, Jun Gu, Jilei Huang, Xiaorong Wan, Yixiong Zheng, Caiji Gao
{"title":"Symbiosomal Proteomic Analysis Reveals the Implication of Endosomal Regulators and CAPs in the Formation of Peanut Nodules.","authors":"Zhao Zheng, Wenjing Ke, Chuanliang Liu, Haomin Cai, Danting Zhu, Qingren Liu, Chuhan Ji, Lei Feng, Jun Gu, Jilei Huang, Xiaorong Wan, Yixiong Zheng, Caiji Gao","doi":"10.1111/ppl.70409","DOIUrl":null,"url":null,"abstract":"<p><p>Arachis hypogaea (peanut) is an important leguminous crop that obtains nitrogen through symbiotic nitrogen fixation with rhizobia, with root nodules serving as the site of this symbiosis. Although the cytological characteristics and ultrastructure of root nodules in model leguminous plants have been well elucidated, research progress on peanut root nodules remains relatively limited. In this study, we characterized the spatiotemporal developmental pattern of peanut root nodules through microscopic imaging and ultrastructural analysis. Furthermore, we isolated symbiosome-enriched fractions from peanut nodules for proteomic analysis and identified 340 and 182 peanut proteins in a comprehensive proteome atlas of the peanut symbiosome membrane (SM) and peribacteroid space (PBS), respectively. Notably, our analysis revealed a significant enrichment of endosomal regulators in the SM and CAP family proteins (cysteine-rich secretory proteins, antigen 5, and pathogenesis-related 1 proteins) in the PBS. Finally, we demonstrated that AhCAP21 specifically localizes to the symbiosome, and the SM-localized AhRabA2a is essential for proper symbiosome development. Together, these findings advance our understanding of peanut nodule development and provide insights into the protein compositions and regulators in symbiosome biogenesis in peanut nodules.</p>","PeriodicalId":20164,"journal":{"name":"Physiologia plantarum","volume":"177 4","pages":"e70409"},"PeriodicalIF":5.4000,"publicationDate":"2025-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Physiologia plantarum","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1111/ppl.70409","RegionNum":2,"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

Arachis hypogaea (peanut) is an important leguminous crop that obtains nitrogen through symbiotic nitrogen fixation with rhizobia, with root nodules serving as the site of this symbiosis. Although the cytological characteristics and ultrastructure of root nodules in model leguminous plants have been well elucidated, research progress on peanut root nodules remains relatively limited. In this study, we characterized the spatiotemporal developmental pattern of peanut root nodules through microscopic imaging and ultrastructural analysis. Furthermore, we isolated symbiosome-enriched fractions from peanut nodules for proteomic analysis and identified 340 and 182 peanut proteins in a comprehensive proteome atlas of the peanut symbiosome membrane (SM) and peribacteroid space (PBS), respectively. Notably, our analysis revealed a significant enrichment of endosomal regulators in the SM and CAP family proteins (cysteine-rich secretory proteins, antigen 5, and pathogenesis-related 1 proteins) in the PBS. Finally, we demonstrated that AhCAP21 specifically localizes to the symbiosome, and the SM-localized AhRabA2a is essential for proper symbiosome development. Together, these findings advance our understanding of peanut nodule development and provide insights into the protein compositions and regulators in symbiosome biogenesis in peanut nodules.

共生体蛋白质组学分析揭示了内体调节因子和cap在花生根瘤形成中的意义。
花生(Arachis hypogaea)是一种重要的豆科作物,通过与根瘤菌的共生固氮获得氮,根瘤是这种共生的场所。虽然豆科植物根瘤的细胞学特征和超微结构已经很好地阐明,但花生根瘤的研究进展相对有限。本研究通过显微成像和超微结构分析,对花生根瘤的时空发育模式进行了研究。此外,我们从花生结节中分离出富含共生体的部分进行蛋白质组学分析,并在花生共生体膜(SM)和类细菌周围空间(PBS)的综合蛋白质组图谱中分别鉴定出340和182个花生蛋白。值得注意的是,我们的分析显示,PBS中SM和CAP家族蛋白(富含半胱氨酸的分泌蛋白、抗原5和致病相关蛋白)的内体调节因子显著富集。最后,我们证明了AhCAP21特异性定位于共生体,而sm定位的AhRabA2a对于共生体的正常发育至关重要。总之,这些发现促进了我们对花生结节发育的理解,并为花生结节共生体生物发生中的蛋白质组成和调节因子提供了见解。
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
Physiologia plantarum
Physiologia plantarum 生物-植物科学
CiteScore
11.00
自引率
3.10%
发文量
224
审稿时长
3.9 months
期刊介绍: Physiologia Plantarum is an international journal committed to publishing the best full-length original research papers that advance our understanding of primary mechanisms of plant development, growth and productivity as well as plant interactions with the biotic and abiotic environment. All organisational levels of experimental plant biology – from molecular and cell biology, biochemistry and biophysics to ecophysiology and global change biology – fall within the scope of the journal. The content is distributed between 5 main subject areas supervised by Subject Editors specialised in the respective domain: (1) biochemistry and metabolism, (2) ecophysiology, stress and adaptation, (3) uptake, transport and assimilation, (4) development, growth and differentiation, (5) photobiology and photosynthesis.
×
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