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在芽殖酵母中,一个凸起的茎将Est1p与端粒酶RNA相连。

A bulged stem tethers Est1p to telomerase RNA in budding yeast.

作者信息

Seto Anita G, Livengood April J, Tzfati Yehuda, Blackburn Elizabeth H, Cech Thomas R

机构信息

Department of Chemistry and Biochemistry, University of Colorado, Boulder, Colorado 80309-0215, USA.

出版信息

Genes Dev. 2002 Nov 1;16(21):2800-12. doi: 10.1101/gad.1029302.

Abstract

It is well established that the template for telomeric DNA synthesis is provided by the RNA subunit of telomerase; however, the additional functions provided by most of the rest of the RNA (>1000 nucleotides in budding yeast) are largely unknown. By alignment of telomerase RNAs of Saccharomyces cerevisiae and six Kluyveromyces species followed by mutagenesis of the S. cerevisiae RNA, we found a conserved region that is essential for telomere maintenance. Phylogenetic analysis and computer folding revealed that this region is conserved not only in primary nucleotide sequence but also in secondary structure. A common bulged-stem structure was predicted in all seven yeast species. Mutational analysis showed the structure to be essential for telomerase function. Suppression of bulged-stem mutant phenotypes by overexpression of Est1p and loss of co-immunoprecipitation of the mutant RNAs with Est1p indicated that this bulged stem is necessary for association of Est1p, a telomerase regulatory subunit. Est1p in yeast extract bound specifically to a small RNA containing the bulged stem, suggesting a direct interaction. We propose that this RNA structure links the enzymatic core of telomerase with Est1p, thereby allowing Est1p to recruit or activate telomerase at the telomere.

摘要

众所周知,端粒酶的RNA亚基为端粒DNA合成提供模板;然而,RNA其余大部分(芽殖酵母中超过1000个核苷酸)所提供的其他功能在很大程度上尚不清楚。通过对酿酒酵母和六种克鲁维酵母属物种的端粒酶RNA进行比对,随后对酿酒酵母RNA进行诱变,我们发现了一个对端粒维持至关重要的保守区域。系统发育分析和计算机折叠显示,该区域不仅在初级核苷酸序列中保守,而且在二级结构中也保守。在所有七个酵母物种中都预测到了一种常见的茎环结构。突变分析表明该结构对端粒酶功能至关重要。通过过表达Est1p抑制茎环突变体表型,以及突变RNA与Est1p的共免疫沉淀丧失,表明这种茎环结构对于端粒酶调节亚基Est1p的结合是必要的。酵母提取物中的Est1p特异性结合含有茎环的小RNA,表明存在直接相互作用。我们提出,这种RNA结构将端粒酶的酶核心与Est1p联系起来,从而使Est1p能够在端粒处募集或激活端粒酶。

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