剪接体对分支位点的识别。

IF 4.2 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
RNA Pub Date : 2024-10-16 DOI:10.1261/rna.080198.124
Jonas Tholen
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引用次数: 0

摘要

剪接体是真核生物的一种多兆位核糖体 RNA 蛋白复合物,可从转录本中去除内含子。剪接体通过多重识别事件确保每个外显子-内含子边界的选择。最初,5'剪接位点(5' SS)和分支位点(BS)分别由 U1 小核核糖核蛋白(snRNP)和 U2 snRNP 结合,而 3' SS 则主要由是否靠近分支位点决定。在 snRNPs 通过碱基配对 snRNA 与转录本稳定结合之前,大量剪接因子会识别剪接位点并招募 snRNPs。这一过程的保真度至关重要,因为剪接因子和 U2 snRNP 成分的突变与许多疾病相关。近年来,在了解酵母和人类如何选择剪接位点方面取得了重大进展。在此,我将回顾并讨论目前对剪接体识别剪接位点的理解,重点是人类中 U2 snRNP 对分支位点的识别和结合。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Branch site recognition by the spliceosome.

The spliceosome is a eukaryotic multimegadalton RNA-protein complex that removes introns from transcripts. The spliceosome ensures the selection of each exon-intron boundary through multiple recognition events. Initially, the 5' splice site (5' SS) and branch site (BS) are bound by the U1 small nuclear ribonucleoprotein (snRNP) and the U2 snRNP, respectively, while the 3' SS is mostly determined by proximity to the branch site. A large number of splicing factors recognize the splice sites and recruit the snRNPs before the stable binding of the snRNPs occurs by base-pairing the snRNA to the transcript. Fidelity of this process is crucial, as mutations in splicing factors and U2 snRNP components are associated with many diseases. In recent years, major advances have been made in understanding how splice sites are selected in Saccharomyces cerevisiae and humans. Here, I review and discuss the current understanding of the recognition of splice sites by the spliceosome with a focus on recognition and binding of the branch site by the U2 snRNP in humans.

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来源期刊
RNA
RNA 生物-生化与分子生物学
CiteScore
8.30
自引率
2.20%
发文量
101
审稿时长
2.6 months
期刊介绍: RNA is a monthly journal which provides rapid publication of significant original research in all areas of RNA structure and function in eukaryotic, prokaryotic, and viral systems. It covers a broad range of subjects in RNA research, including: structural analysis by biochemical or biophysical means; mRNA structure, function and biogenesis; alternative processing: cis-acting elements and trans-acting factors; ribosome structure and function; translational control; RNA catalysis; tRNA structure, function, biogenesis and identity; RNA editing; rRNA structure, function and biogenesis; RNA transport and localization; regulatory RNAs; large and small RNP structure, function and biogenesis; viral RNA metabolism; RNA stability and turnover; in vitro evolution; and RNA chemistry.
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