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基因组解偶联蛋白1与质体RNA结合并促进其成熟。

GENOMES UNCOUPLED PROTEIN1 binds to plastid RNAs and promotes their maturation.

作者信息

Tang Qian, Xu Duorong, Lenzen Benjamin, Brachmann Andreas, Yapa Madhura M, Doroodian Paymon, Schmitz-Linneweber Christian, Masuda Tatsuru, Hua Zhihua, Leister Dario, Kleine Tatjana

机构信息

Plant Molecular Biology (Botany), Faculty of Biology, Ludwig-Maximilians-University München, 82152 Martinsried, Germany.

Molecular Genetics, Humboldt-University Berlin, Philippstr. 13, 10115 Berlin, Germany.

出版信息

Plant Commun. 2024 Dec 9;5(12):101069. doi: 10.1016/j.xplc.2024.101069. Epub 2024 Aug 22.

DOI:10.1016/j.xplc.2024.101069
PMID:39169625
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11671767/
Abstract

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 pentatricopeptide repeat code-based prediction and experimental validation by RNA immunoprecipitation experiments, we identified several putative targets of GUN1, 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 on mechanisms of plastid gene expression and will help to elucidate the function of GUN1 in retrograde signaling.

摘要

质体生物发生以及通过正向和逆向信号传导对质体与核基因组表达进行协调,对植物发育至关重要。GENOMES UNCOUPLED1(GUN1)在植物早期发育的逆向信号传导中起核心作用。GUN1的假定功能已得到广泛研究,但其分子功能仍存在争议。在这里,我们评估已发表的转录组数据,并从在信号相关条件下生长的gun1突变体中生成我们自己的数据,以表明编辑和剪接与GUN1依赖的逆向信号传导无关。我们对具有白色和浅色子叶的gun1幼苗的质体(后)转录组的研究表明,GUN1缺陷会显著改变整个质体转录组。通过将这一结果与基于五肽重复序列密码的预测以及RNA免疫沉淀实验的实验验证相结合,我们确定了几个GUN1的假定靶标,包括tRNA以及源自ycf1.2、rpoC1和rpoC2的RNA,还有ndhH-ndhA-ndhI-ndhG-ndhE-psaC-ndhD基因簇。白色gun1突变体中质体rRNA的缺失以及几乎所有质体转录本的显著减少导致了子叶表型。我们的研究为RNA结合和成熟作为长期寻找的GUN1分子功能提供了证据,并解决了长期存在的争议。我们预计,我们的发现将为后续关于质体基因表达机制的研究奠定基础,并有助于阐明GUN1在逆向信号传导中的功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0070/11671767/e7ccf825c51e/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0070/11671767/6be47405ead2/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0070/11671767/da4a18d3717f/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0070/11671767/31875bad2194/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0070/11671767/49b19f68c090/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0070/11671767/c828329ed86f/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0070/11671767/4209b41214a5/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0070/11671767/e7ccf825c51e/gr7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0070/11671767/6be47405ead2/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0070/11671767/da4a18d3717f/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0070/11671767/31875bad2194/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0070/11671767/49b19f68c090/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0070/11671767/c828329ed86f/gr5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0070/11671767/4209b41214a5/gr6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0070/11671767/e7ccf825c51e/gr7.jpg

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