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一种新型剪接因子Yju2与NTC相关,并在Prp2之后发挥作用,促进前体mRNA剪接的首次催化反应。

A novel splicing factor, Yju2, is associated with NTC and acts after Prp2 in promoting the first catalytic reaction of pre-mRNA splicing.

作者信息

Liu Yen-Chi, Chen Hsin-Chou, Wu Nan-Ying, Cheng Soo-Chen

机构信息

Institute of Microbiology Biology and Immunology, National Yang-Ming University, Taipei, Taiwan.

出版信息

Mol Cell Biol. 2007 Aug;27(15):5403-13. doi: 10.1128/MCB.00346-07. Epub 2007 May 21.

Abstract

The Prp19-associated complex (NTC) is essential for pre-mRNA splicing and is associated with the spliceosome during spliceosome activation. NTC is required for specifying interactions of U5 and U6 with pre-mRNA to stabilize their association with the spliceosome after dissociation of U4. Here, we show that a novel splicing factor, Yju2, is associated with components of NTC, and that it is required for pre-mRNA splicing both in vivo and in vitro. During spliceosome assembly, Yju2 is associated with the spliceosome at nearly the same time as NTC but is destabilized after the first catalytic reaction, whereas other NTC components remain associated until the reaction is complete. Extracts depleted of Yju2 could be complemented by recombinant Yju2, suggesting that Yju2 and NTC are not entirely in association with each other. Yju2 is not required for the binding of NTC to the spliceosome or for NTC-mediated spliceosome activation. Complementation analysis of the affinity-isolated spliceosome formed in Yju2-depleted extracts demonstrated that Yju2 acts in concert with an unidentified heat-resistant factor(s) in an ATP-independent manner to promote the first catalytic reaction of pre-mRNA splicing after Prp2-mediated structural rearrangement of the spliceosome.

摘要

与Prp19相关的复合物(NTC)对于前体mRNA剪接至关重要,并且在剪接体激活过程中与剪接体相关联。NTC对于确定U5和U6与前体mRNA的相互作用是必需的,以便在U4解离后稳定它们与剪接体的结合。在这里,我们表明一种新的剪接因子Yju2与NTC的组分相关联,并且它在体内和体外的前体mRNA剪接中都是必需的。在剪接体组装过程中,Yju2与NTC几乎同时与剪接体相关联,但在第一次催化反应后变得不稳定,而其他NTC组分在反应完成之前一直保持相关联。缺乏Yju2的提取物可以用重组Yju2进行补充,这表明Yju2和NTC并非完全相互关联。Yju2对于NTC与剪接体的结合或NTC介导的剪接体激活不是必需的。对在缺乏Yju2的提取物中形成的亲和分离剪接体的互补分析表明,Yju2以ATP非依赖的方式与一种未鉴定的耐热因子协同作用,以促进在Prp2介导的剪接体结构重排后前体mRNA剪接的第一次催化反应。

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