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PTB介导的新型剪接抑制模式。

Novel modes of splicing repression by PTB.

作者信息

Spellman Rachel, Smith Christopher W J

机构信息

Department of Biochemistry, University of Cambridge, 80 Tennis Court Road, Cambridge CB2 1GA, UK.

出版信息

Trends Biochem Sci. 2006 Feb;31(2):73-6. doi: 10.1016/j.tibs.2005.12.003. Epub 2006 Jan 5.

Abstract

Polypyrimidine-tract-binding protein (PTB) is a repressive regulator of alternative splicing. Models for PTB activity have ranged from simple binding competition with splicing factor U2AF(65) at regulated polypyrimidine tracts to looping out of repressed exons by binding of PTB to flanking sites. Structural analysis of PTB bound to RNA suggests how PTB monomers can induce loops, but two recent publications indicate that repression by PTB involves more than just binding to RNA.

摘要

多嘧啶序列结合蛋白(PTB)是一种可变剪接的抑制性调节因子。PTB活性的模型范围从在受调控的多嘧啶序列处与剪接因子U2AF(65)进行简单的结合竞争,到通过PTB与侧翼位点的结合使被抑制的外显子形成环化。与RNA结合的PTB的结构分析揭示了PTB单体如何诱导环化,但最近的两篇论文表明,PTB的抑制作用不仅仅涉及与RNA的结合。

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