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拟南芥 U1 snRNP 调控 mRNA 3'-末端加工。

The Arabidopsis U1 snRNP regulates mRNA 3'-end processing.

机构信息

Institute of Biology and Environmental Sciences, University of Oldenburg, Oldenburg, Germany.

Max Planck Institute for Plant Breeding Research (MPIPZ), Cologne, Germany.

出版信息

Nat Plants. 2024 Oct;10(10):1514-1531. doi: 10.1038/s41477-024-01796-8. Epub 2024 Sep 23.

Abstract

The removal of introns by the spliceosome is a key gene regulatory mechanism in eukaryotes, with the U1 snRNP subunit playing a crucial role in the early stages of splicing. Studies in metazoans show that the U1 snRNP also conducts splicing-independent functions, but the lack of genetic tools and knowledge about U1 snRNP-associated proteins have limited the study of such splicing-independent functions in plants. Here we describe an RNA-centric approach that identified more than 200 proteins associated with the Arabidopsis U1 snRNP and revealed a tight link to mRNA cleavage and polyadenylation factors. Interestingly, we found that the U1 snRNP protects mRNAs against premature cleavage and polyadenylation within introns-a mechanism known as telescripting in metazoans-while also influencing alternative polyadenylation site selection in 3'-UTRs. Overall, our work provides a comprehensive view of U1 snRNP interactors and reveals novel functions in regulating mRNA 3'-end processing in Arabidopsis, laying the groundwork for understanding non-canonical functions of plant U1 snRNPs.

摘要

剪接体通过切除内含子来实现真核生物的基因调控,其中 U1 snRNP 亚基在剪接的早期阶段发挥着关键作用。后生动物的研究表明,U1 snRNP 还具有非依赖性剪接功能,但缺乏遗传工具和与 U1 snRNP 相关蛋白的知识限制了对植物中非依赖性剪接功能的研究。在这里,我们描述了一种基于 RNA 的方法,该方法鉴定了 200 多种与拟南芥 U1 snRNP 相关的蛋白质,并揭示了与 mRNA 切割和多聚腺苷酸化因子的紧密联系。有趣的是,我们发现 U1 snRNP 可防止 mRNA 在内含子中过早切割和多聚腺苷酸化,这种机制在后生动物中称为 telescripting,同时还影响 3'UTR 中的可变多聚腺苷酸化位点选择。总的来说,我们的工作提供了 U1 snRNP 相互作用物的全面视图,并揭示了在调节拟南芥 mRNA 3'端加工过程中的新功能,为理解植物 U1 snRNP 的非典型功能奠定了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ebb/11489095/32847fa4082b/41477_2024_1796_Fig1_HTML.jpg

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