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主要酵母端粒结合蛋白Rap1p的C末端增强端粒形成。

The C terminus of the major yeast telomere binding protein Rap1p enhances telomere formation.

作者信息

Ray A, Runge K W

机构信息

Department of Molecular Biology, Lerner Research Institute, Cleveland Clinic Foundation, Ohio 44195, USA.

出版信息

Mol Cell Biol. 1998 Mar;18(3):1284-95. doi: 10.1128/MCB.18.3.1284.

Abstract

The telomeres of most organisms consist of short repeated sequences that can be elongated by telomerase, a reverse transcriptase complex that contains its own RNA template for the synthesis of telomere repeats. In Saccharomyces cerevisiae, the RAP1 gene encodes the major telomere binding protein Rap1p. Here we use a quantitative telomere formation assay to demonstrate that Rap1p C termini can enhance telomere formation more than 30-fold when they are located at internal sites. This stimulation is distinct from protection from degradation. Enhancement of formation required the gene for telomerase RNA but not Sir1p, Sir2p, Sir3p, Sir4p, Tel1p, or the Rif1p binding site in the Raplp C terminus. Our data suggest that Rap1p C termini enhance telomere formation by attracting or increasing the activity of telomerase near telomeres. Earlier work suggests that Rap1p molecules at the chromosome terminus inhibit the elongation of long telomeres by blocking the access of telomerase. Our results suggest a model where a balance between internal Rap1p increasing telomerase activity and Rap1p at the termini of long telomeres controlling telomerase access maintains telomeres at a constant length.

摘要

大多数生物体的端粒由短重复序列组成,这些序列可被端粒酶延长,端粒酶是一种逆转录酶复合体,它含有自身用于合成端粒重复序列的RNA模板。在酿酒酵母中,RAP1基因编码主要的端粒结合蛋白Rap1p。在此,我们使用定量端粒形成试验来证明,当Rap1p的C末端位于内部位点时,它们增强端粒形成的能力可超过30倍。这种刺激不同于防止降解。形成的增强需要端粒酶RNA基因,但不需要Sir1p、Sir2p、Sir3p、Sir4p、Tel1p或Rap1p C末端中的Rif1p结合位点。我们的数据表明,Rap1p的C末端通过吸引或增加端粒附近端粒酶的活性来增强端粒形成。早期的研究表明,染色体末端的Rap1p分子通过阻止端粒酶的进入来抑制长端粒的延长。我们的结果提出了一个模型,即内部Rap1p增加端粒酶活性与长端粒末端的Rap1p控制端粒酶进入之间的平衡维持端粒长度恒定。

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