GENOMES UNCOUPLED PROTEIN1 与质体 RNA 结合并促进其成熟。

IF 9.4 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Qian Tang, Duorong Xu, Benjamin Lenzen, Andreas Brachmann, Madhura M Yapa, Paymon Doroodian, Christian Schmitz-Linneweber, Tatsuru Masuda, Zhihua Hua, Dario Leister, Tatjana Kleine
{"title":"GENOMES UNCOUPLED PROTEIN1 与质体 RNA 结合并促进其成熟。","authors":"Qian Tang, Duorong Xu, Benjamin Lenzen, Andreas Brachmann, Madhura M Yapa, Paymon Doroodian, Christian Schmitz-Linneweber, Tatsuru Masuda, Zhihua Hua, Dario Leister, Tatjana Kleine","doi":"10.1016/j.xplc.2024.101069","DOIUrl":null,"url":null,"abstract":"<p><p>Plastid biogenesis and the coordination of plastid and nuclear genome expression through anterograde and retrograde signaling are essential for plant development. GENOMES UNCOUPLED1 (GUN1) plays a central role in retrograde signaling during early plant development. The putative function of GUN1 has been extensively studied, but its molecular function remains controversial. Here, we evaluate published transcriptome data and generate our own data from gun1 mutants grown under signaling relevant conditions to show that editing and splicing are not relevant for GUN1-dependent retrograde signaling. Our study of the plastid (post)-transcriptome of gun1 seedlings with white and pale cotyledons demonstrates that GUN1 deficiency significantly alters the entire plastid transcriptome. By combining this result with a PPR code-based prediction and experimental validation by RNA immunoprecipitation experiments, several putative targets of GUN1 were identified, including tRNAs and RNAs derived from ycf1.2, rpoC1 and rpoC2, and the ndhH-ndhA-ndhI-ndhG-ndhE-psaC-ndhD gene cluster. The absence of plastid rRNAs and the significant reduction of almost all plastid transcripts in white gun1 mutants account for the cotyledon phenotype. Our study provides evidence for RNA binding and maturation as the long-sought molecular function of GUN1 and resolves long-standing controversies. We anticipate that our findings will serve as a basis for subsequent studies investigating the mechanism of plastid gene expression and will facilitate the elucidation of GUN1's function in retrograde signaling.</p>","PeriodicalId":52373,"journal":{"name":"Plant Communications","volume":null,"pages":null},"PeriodicalIF":9.4000,"publicationDate":"2024-08-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"GENOMES UNCOUPLED PROTEIN1 binds to plastid RNAs and promotes their maturation.\",\"authors\":\"Qian Tang, Duorong Xu, Benjamin Lenzen, Andreas Brachmann, Madhura M Yapa, Paymon Doroodian, Christian Schmitz-Linneweber, Tatsuru Masuda, Zhihua Hua, Dario Leister, Tatjana Kleine\",\"doi\":\"10.1016/j.xplc.2024.101069\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Plastid biogenesis and the coordination of plastid and nuclear genome expression through anterograde and retrograde signaling are essential for plant development. GENOMES UNCOUPLED1 (GUN1) plays a central role in retrograde signaling during early plant development. The putative function of GUN1 has been extensively studied, but its molecular function remains controversial. Here, we evaluate published transcriptome data and generate our own data from gun1 mutants grown under signaling relevant conditions to show that editing and splicing are not relevant for GUN1-dependent retrograde signaling. Our study of the plastid (post)-transcriptome of gun1 seedlings with white and pale cotyledons demonstrates that GUN1 deficiency significantly alters the entire plastid transcriptome. By combining this result with a PPR code-based prediction and experimental validation by RNA immunoprecipitation experiments, several putative targets of GUN1 were identified, including tRNAs and RNAs derived from ycf1.2, rpoC1 and rpoC2, and the ndhH-ndhA-ndhI-ndhG-ndhE-psaC-ndhD gene cluster. The absence of plastid rRNAs and the significant reduction of almost all plastid transcripts in white gun1 mutants account for the cotyledon phenotype. Our study provides evidence for RNA binding and maturation as the long-sought molecular function of GUN1 and resolves long-standing controversies. We anticipate that our findings will serve as a basis for subsequent studies investigating the mechanism of plastid gene expression and will facilitate the elucidation of GUN1's function in retrograde signaling.</p>\",\"PeriodicalId\":52373,\"journal\":{\"name\":\"Plant Communications\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":9.4000,\"publicationDate\":\"2024-08-21\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Plant Communications\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1016/j.xplc.2024.101069\",\"RegionNum\":1,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Communications","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/j.xplc.2024.101069","RegionNum":1,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0

摘要

质体的生物发生以及通过前向和逆向信号协调质体和核基因组的表达对植物的发育至关重要。GENOMES UNCOUPLED1(GUN1)在植物早期发育过程中的逆行信号传递中发挥着核心作用。GUN1 的推测功能已被广泛研究,但其分子功能仍存在争议。在此,我们评估了已发表的转录组数据,并从信号相关条件下生长的 gun1 突变体中生成了我们自己的数据,以证明编辑和剪接与 GUN1 依赖性逆行信号无关。我们对具有白色和苍白子叶的 gun1 幼苗的质体(后)转录组的研究表明,GUN1 缺乏会显著改变整个质体转录组。通过将这一结果与基于 PPR 代码的预测和 RNA 免疫沉淀实验的验证相结合,确定了 GUN1 的几个假定靶标,包括 tRNA 和来自 ycf1.2、rpoC1 和 rpoC2 以及 ndhH-ndhA-ndhI-ndhG-ndhE-psaC-ndhD 基因簇的 RNA。白枪1突变体中质体rRNA的缺失和几乎所有质体转录本的显著减少是子叶表型的原因。我们的研究为 GUN1 的分子功能--RNA 结合和成熟--提供了证据,并解决了长期存在的争议。我们预计,我们的研究结果将成为后续研究质体基因表达机制的基础,并将有助于阐明 GUN1 在逆向信号转导中的功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
GENOMES UNCOUPLED PROTEIN1 binds to plastid RNAs and promotes their maturation.

Plastid biogenesis and the coordination of plastid and nuclear genome expression through anterograde and retrograde signaling are essential for plant development. GENOMES UNCOUPLED1 (GUN1) plays a central role in retrograde signaling during early plant development. The putative function of GUN1 has been extensively studied, but its molecular function remains controversial. Here, we evaluate published transcriptome data and generate our own data from gun1 mutants grown under signaling relevant conditions to show that editing and splicing are not relevant for GUN1-dependent retrograde signaling. Our study of the plastid (post)-transcriptome of gun1 seedlings with white and pale cotyledons demonstrates that GUN1 deficiency significantly alters the entire plastid transcriptome. By combining this result with a PPR code-based prediction and experimental validation by RNA immunoprecipitation experiments, several putative targets of GUN1 were identified, including tRNAs and RNAs derived from ycf1.2, rpoC1 and rpoC2, and the ndhH-ndhA-ndhI-ndhG-ndhE-psaC-ndhD gene cluster. The absence of plastid rRNAs and the significant reduction of almost all plastid transcripts in white gun1 mutants account for the cotyledon phenotype. Our study provides evidence for RNA binding and maturation as the long-sought molecular function of GUN1 and resolves long-standing controversies. We anticipate that our findings will serve as a basis for subsequent studies investigating the mechanism of plastid gene expression and will facilitate the elucidation of GUN1's function in retrograde signaling.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Plant Communications
Plant Communications Agricultural and Biological Sciences-Plant Science
CiteScore
15.70
自引率
5.70%
发文量
105
审稿时长
6 weeks
期刊介绍: Plant Communications is an open access publishing platform that supports the global plant science community. It publishes original research, review articles, technical advances, and research resources in various areas of plant sciences. The scope of topics includes evolution, ecology, physiology, biochemistry, development, reproduction, metabolism, molecular and cellular biology, genetics, genomics, environmental interactions, biotechnology, breeding of higher and lower plants, and their interactions with other organisms. The goal of Plant Communications is to provide a high-quality platform for the dissemination of plant science research.
×
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:481959085
Book学术官方微信