首页> 外文期刊>Genes and Development: a Journal Devoted to the Molecular Analysis of Gene Expression in Eukaryotes, Prokaryotes, and Viruses >Spliceosome activation: U4 is the path, stem I is the goal, and Prp8 is the keeper. let's cheer for the ATPase Brr2!
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Spliceosome activation: U4 is the path, stem I is the goal, and Prp8 is the keeper. let's cheer for the ATPase Brr2!

机译:剪接体激活:U4是路径,茎I是目标,Prp8是守护者。让我们为ATPase Brr2加油吧!

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摘要

During pre-mRNA splicing, the spliceosome is activated for catalysis by unwinding base-paired U4/U6 small nuclear RNAs, a step that must be precisely timed. We know that unwinding requires the ATPase Brr2, but the mechanism and regulation of unwinding have been understood poorly. In the November 1, 2012, issue of Genes & Development, Hahn and colleagues (pp. 2408-2421) and Mozaffari-Jovin and colleagues (pp. 2422-2434) defined a pathway for U4/U6 un winding. Moreover, Mozaffari-Jovin and colleagues suggested a mechanism for regulating Brr2.
机译:在mRNA前期剪接过程中,通过展开碱基配对的U4 / U6小核RNA来激活剪接体以进行催化,这一步骤必须精确计时。我们知道放卷需要ATPase Brr2,但是对放卷的机制和调控了解得很少。在2012年11月1日的《基因与发展》上,Hahn及其同事(第2408-2421页)和Mozaffari-Jovin及其同事(第2422-2434页)定义了U4 / U6展开的途径。此外,Mozaffari-Jovin及其同事提出了一种调节Brr2的机制。

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