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snRNA 在剪接体催化中的作用。

The role of snRNAs in spliceosomal catalysis.

机构信息

Department of Biochemistry, Case Western Reserve University, Cleveland, Ohio, USA.

出版信息

Prog Mol Biol Transl Sci. 2013;120:195-228. doi: 10.1016/B978-0-12-381286-5.00006-8.

Abstract

The spliceosomes, large ribonucleoprotein (RNP) assemblies that remove the intervening sequences from pre-mRNAs, contain a large number of proteins and five small nuclear RNAs (snRNAs). One snRNA, U6, contains highly conserved sequences that are thought to be the functional counterparts of the RNA elements that form the active site of self-splicing group II intron ribozymes. An in vitro-assembled, protein-free complex of U6 with U2, the base-pairing partner in the spliceosomal catalytic core, can catalyze a two-step splicing reaction in the absence of all other spliceosomal factors, suggesting that the two snRNAs may form all or a large share of the spliceosomal active site. On the other hand, several spliceosomal proteins are thought to help in the formation of functionally required RNA-RNA interactions in the catalytic core. Whether they also contribute functional groups to the spliceosomal active site, and thus whether the spliceosomes are RNA or RNP enzymes remain uncertain.

摘要

剪接体是一种大型核糖核蛋白(RNP)复合物,能够从前体 mRNA 中切除内含子序列,其中包含大量蛋白质和五种小核 RNA(snRNA)。一种 snRNA,U6,含有高度保守的序列,被认为是形成自我剪接 II 类内含子核酶活性部位的 RNA 元件的功能对应物。在体外组装的、无蛋白质的 U6 与 U2 复合物,U2 是剪接体催化核心的碱基配对伙伴,可在没有其他剪接体因子的情况下催化两步剪接反应,这表明这两个 snRNA 可能形成剪接体活性部位的全部或大部分。另一方面,一些剪接体蛋白被认为有助于在催化核心中形成功能必需的 RNA-RNA 相互作用。它们是否也为剪接体活性部位提供功能基团,以及剪接体是否是 RNA 或 RNP 酶仍然不确定。

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