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人端粒酶RNA中假结结构的功能分析

Functional analysis of the pseudoknot structure in human telomerase RNA.

作者信息

Chen Jiunn-Liang, Greider Carol W

机构信息

Department of Chemistry and Biochemistry and School of Life Sciences, Arizona State University, Tempe, AZ 85287, USA.

出版信息

Proc Natl Acad Sci U S A. 2005 Jun 7;102(23):8080-5; discussion 8077-9. doi: 10.1073/pnas.0502259102. Epub 2005 Apr 22.

Abstract

Telomerase is essential for maintaining telomere length and chromosome stability in stem cells, germline cells, and cancer cells. The telomerase ribonucleoprotein complex consists of two essential components, a catalytic protein component and an RNA molecule that provides the template for telomeric repeat synthesis. A pseudoknot structure in the human telomerase RNA is conserved in all vertebrates and is essential for telomerase activity. It has been proposed that this highly conserved structure functions as a dynamic structure with conformational interchange between the pseudoknot and a hairpin with intraloop base pairings. To examine the structural and functional requirements of the pseudoknot structure, we made mutations in the proposed base-paired regions in the pseudoknot. Although mutations that disrupted the pseudoknot P3 helix abolished activity as predicted, mutations that disrupted the intraloop hairpin base pairings did not reduce telomerase activity, indicating that the intraloop hairpin is not required for telomerase function. This functional study thus provides evidence against the previous proposed molecular-switch model of telomerase pseudoknot function and supports a static pseudoknot structure. The mutational analysis further suggests that telomerase RNA can function independent of the proposed intermolecular pairings between pseudoknot regions on two RNA molecules.

摘要

端粒酶对于维持干细胞、生殖细胞和癌细胞中的端粒长度及染色体稳定性至关重要。端粒酶核糖核蛋白复合体由两个关键组分构成,一个催化蛋白组分和一个为端粒重复序列合成提供模板的RNA分子。人类端粒酶RNA中的假结结构在所有脊椎动物中都保守,并且对端粒酶活性至关重要。有人提出,这种高度保守的结构作为一种动态结构发挥作用,在假结和具有环内碱基配对的发夹之间存在构象互换。为了研究假结结构的结构和功能要求,我们对假结中提议的碱基配对区域进行了突变。尽管破坏假结P3螺旋的突变如预期那样消除了活性,但破坏环内发夹碱基配对的突变并未降低端粒酶活性,这表明端粒酶功能不需要环内发夹。因此,这项功能研究提供了证据,反对先前提出的端粒酶假结功能的分子开关模型,并支持一种静态假结结构。突变分析进一步表明,端粒酶RNA可以独立于两个RNA分子上假结区域之间提议的分子间配对发挥功能。

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本文引用的文献

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