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酵母剪接体五聚体小核核糖核蛋白的组成与功能特性

Composition and functional characterization of the yeast spliceosomal penta-snRNP.

作者信息

Stevens Scott W, Ryan Daniel E, Ge Helen Y, Moore Roger E, Young Mary K, Lee Terry D, Abelson John

机构信息

California Institute of Technology, Division of Biology 147-75, Pasadena, CA 91125, USA.

出版信息

Mol Cell. 2002 Jan;9(1):31-44. doi: 10.1016/s1097-2765(02)00436-7.

Abstract

Pre-mRNA introns are spliced in a macromolecular machine, the spliceosome. For each round of splicing, the spliceosome assembles de novo in a series of ATP-dependent steps involving numerous changes in RNA-RNA and RNA-protein interactions. As currently understood, spliceosome assembly proceeds by addition of discrete U1, U2, and U4/U6*U5 snRNPs to a pre-mRNA substrate to form functional splicing complexes. We characterized a 45S yeast penta-snRNP which contains all five spliceosomal snRNAs and over 60 pre-mRNA splicing factors. The particle is functional in extracts and, when supplied with soluble factors, is capable of splicing pre-mRNA. We propose that the spliceosomal snRNPs associate prior to binding of a pre-mRNA substrate rather than with pre-mRNA via stepwise addition of discrete snRNPs.

摘要

前体mRNA内含子在一种大分子机器——剪接体中进行剪接。对于每一轮剪接,剪接体在一系列依赖ATP的步骤中从头组装,这涉及RNA-RNA和RNA-蛋白质相互作用的众多变化。按照目前的理解,剪接体组装是通过将离散的U1、U2和U4/U6*U5 snRNP添加到前体mRNA底物上以形成功能性剪接复合体来进行的。我们鉴定了一种45S酵母五聚体snRNP,它包含所有五种剪接体snRNA和60多种前体mRNA剪接因子。该颗粒在提取物中具有功能,并且当提供可溶性因子时,能够剪接前体mRNA。我们提出,剪接体snRNP在结合前体mRNA底物之前就相互结合,而不是通过逐步添加离散的snRNP与前体mRNA结合。

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