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加帽、剪接和3' 加工分别由RNA聚合酶II刺激:CTD不同区段具有不同功能。

Capping, splicing, and 3' processing are independently stimulated by RNA polymerase II: different functions for different segments of the CTD.

作者信息

Fong N, Bentley D L

机构信息

Department of Biochemistry and Molecular Genetics, University of Colorado Health Science Center (UCHSC), Denver, Colorado 80262, USA.

出版信息

Genes Dev. 2001 Jul 15;15(14):1783-95. doi: 10.1101/gad.889101.

Abstract

Capping, splicing, and cleavage/polyadenylation of pre-mRNAs are interdependent events that are all stimulated in vivo by the carboxy-terminal domain (CTD) of RNA Pol II. We show that the CTD independently enhances splicing and 3' processing and that stimulation of splicing by enhancers is facilitated by the CTD. We provide evidence that stimulation of 3' processing by the CTD requires contact with the 50-kD subunit of the cleavage stimulation factor, CstF. Overexpression of the CTD-binding domain of CstF p50 had a dominant-negative effect on 3' processing without disrupting the CstF complex. The CTD comprises 52 heptad repeats. The CTD carboxyl terminus including heptads 27-52 supported capping, splicing, and 3' processing but the amino terminus supported only capping. We conclude that the CTD independently stimulates all three major pre-mRNA processing steps and that different regions of the CTD can serve distinct functions in pre-mRNA processing.

摘要

前体mRNA的加帽、剪接以及切割/聚腺苷酸化是相互依存的事件,在体内均受到RNA聚合酶II的羧基末端结构域(CTD)的刺激。我们发现CTD可独立增强剪接和3' 加工过程,并且增强子对剪接的刺激作用因CTD而得到促进。我们提供的证据表明,CTD对3' 加工的刺激作用需要与切割刺激因子CstF的50-kD亚基接触。CstF p50的CTD结合结构域的过表达对3' 加工具有显性负效应,且不会破坏CstF复合体。CTD由52个七肽重复序列组成。包含七肽27 - 52的CTD羧基末端支持加帽、剪接和3' 加工,但氨基末端仅支持加帽。我们得出结论,CTD可独立刺激前体mRNA的所有三个主要加工步骤,并且CTD的不同区域在前体mRNA加工中可发挥不同功能。

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