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RNA Splicing by the Spliceosome.
Annual Review of Biochemistry ( IF 12.1 ) Pub Date : 2020-06-22 , DOI: 10.1146/annurev-biochem-091719-064225
Max E Wilkinson 1 , Clément Charenton 1 , Kiyoshi Nagai 1
Affiliation  

The spliceosome removes introns from messenger RNA precursors (pre-mRNA). Decades of biochemistry and genetics combined with recent structural studies of the spliceosome have produced a detailed view of the mechanism of splicing. In this review, we aim to make this mechanism understandable and provide several videos of the spliceosome in action to illustrate the intricate choreography of splicing. The U1 and U2 small nuclear ribonucleoproteins (snRNPs) mark an intron and recruit the U4/U6.U5 tri-snRNP. Transfer of the 5′ splice site (5′SS) from U1 to U6 snRNA triggers unwinding of U6 snRNA from U4 snRNA. U6 folds with U2 snRNA into an RNA-based active site that positions the 5′SS at two catalytic metal ions. The branch point (BP) adenosine attacks the 5′SS, producing a free 5′ exon. Removal of the BP adenosine from the active site allows the 3′SS to bind, so that the 5′ exon attacks the 3′SS to produce mature mRNA and an excised lariat intron.

中文翻译:


剪接体的RNA剪接。

剪接体从信使RNA前体(pre-mRNA)中去除内含子。数十年的生物化学和遗传学研究以及最近对剪接体的结构研究相结合,对剪接机理进行了详细研究。在这篇综述中,我们旨在使这种机制易于理解,并提供了一些实际的剪接体视频,以说明剪接的复杂编排。U1和U2小核糖核蛋白(snRNPs)标记一个内含子并募集U4 / U6.U5 tri-snRNP。5'剪接位点(5'SS)从U1到U6 snRNA的转移触发U6 snRNA从U4 snRNA展开。U6与U2 snRNA折叠成一个基于RNA的活性位点,该位点将5'SS定位在两个催化金属离子上。分支点(BP)腺苷攻击5'SS,产生游离的5'外显子。

更新日期:2020-06-23
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