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剪接底物与剪接体中的小核核糖核蛋白之间的多种相互作用。

Multiple interactions between the splicing substrate and small nuclear ribonucleoproteins in spliceosomes.

作者信息

Chabot B, Steitz J A

出版信息

Mol Cell Biol. 1987 Jan;7(1):281-93. doi: 10.1128/mcb.7.1.281-293.1987.

Abstract

Protection experiments with antibodies against small nuclear ribonucleoproteins (snRNPs) have elucidated the location of and requirements for interactions between snRNPs and human beta-globin transcripts during splicing in vitro. U2 snRNP association with the intron branch site continues after branch formation, requires intact U2 RNA, and is affected by some alterations of the 3' splice site sequence. U2 snRNP binding to the branched intermediate and U1 snRNP protection of an extended 5' splice region are detected exclusively in spliceosome fractions, indicating that both snRNPs are spliceosome components. While each snRNP associates specifically with the pre-mRNA, they also appear to interact with each other. The recovery of fragments mapping upstream of the 5' splice site suggests how the excised exon is held in the spliceosome.

摘要

针对小核核糖核蛋白(snRNP)的抗体进行的保护实验,阐明了体外剪接过程中snRNP与人类β-珠蛋白转录本之间相互作用的位置和要求。分支形成后,U2 snRNP与内含子分支位点的结合仍在继续,需要完整的U2 RNA,并且会受到3'剪接位点序列某些改变的影响。仅在剪接体组分中检测到U2 snRNP与分支中间体的结合以及U1 snRNP对延伸的5'剪接区域的保护,这表明这两种snRNP都是剪接体的组成部分。虽然每个snRNP都与前体mRNA特异性结合,但它们似乎也相互作用。在5'剪接位点上游定位的片段的回收提示了切除的外显子在剪接体中的保留方式。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cac/365068/d088ca086fd0/molcellb00073-0302-a.jpg

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