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剪接体如何对前体信使 RNA 进行剪接?

How Is Precursor Messenger RNA Spliced by the Spliceosome?

机构信息

Beijing Advanced Innovation Center for Structural Biology, School of Life Sciences and School of Medicine, Tsinghua University, Beijing 100084, China; email:

Institute of Biology, Westlake Institute for Advanced Study, Westlake University, Hangzhou 310024, China.

出版信息

Annu Rev Biochem. 2020 Jun 20;89:333-358. doi: 10.1146/annurev-biochem-013118-111024. Epub 2019 Dec 9.

Abstract

Splicing of the precursor messenger RNA, involving intron removal and exon ligation, is mediated by the spliceosome. Together with biochemical and genetic investigations of the past four decades, structural studies of the intact spliceosome at atomic resolution since 2015 have led to mechanistic delineation of RNA splicing with remarkable insights. The spliceosome is proven to be a protein-orchestrated metalloribozyme. Conserved elements of small nuclear RNA (snRNA) constitute the splicing active site with two catalytic metal ions and recognize three conserved intron elements through duplex formation, which are delivered into the splicing active site for branching and exon ligation. The protein components of the spliceosome stabilize the conformation of the snRNA, drive spliceosome remodeling, orchestrate the movement of the RNA elements, and facilitate the splicing reaction. The overall organization of the spliceosome and the configuration of the splicing active site are strictly conserved between human and yeast.

摘要

前体信使 RNA 的剪接,涉及内含子去除和外显子连接,由剪接体介导。过去四十年的生化和遗传学研究,以及自 2015 年以来对完整剪接体的原子分辨率结构研究,都对 RNA 剪接进行了机制划分,并获得了显著的见解。剪接体被证明是一种由蛋白质协调的金属核酶。小核 RNA(snRNA)的保守元件构成剪接活性位点,其中包含两个催化金属离子,并通过双链体形成识别三个保守的内含子元件,这些元件被递送到剪接活性位点进行分支和外显子连接。剪接体的蛋白质成分稳定 snRNA 的构象,驱动剪接体重构,协调 RNA 元件的运动,并促进剪接反应。剪接体的整体组织和剪接活性位点的结构在人和酵母之间严格保守。

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