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在缺乏端粒酶的情况下,细胞周期调控产生富含鸟嘌呤的单链DNA。

Cell cycle-regulated generation of single-stranded G-rich DNA in the absence of telomerase.

作者信息

Dionne I, Wellinger R J

机构信息

Faculté de Médicine, Départment de Microbiologie et Infectiologie, Université de Sherbrooke, QC, Canada.

出版信息

Proc Natl Acad Sci U S A. 1996 Nov 26;93(24):13902-7. doi: 10.1073/pnas.93.24.13902.

Abstract

Current models of telomere replication predict that due to the properties of the polymerases implicated in semiconservative replication of linear DNA, the two daughter molecules have one end that is blunt and one end with a short 3' overhang. Telomerase is thought to extend the short 3' overhang to produce long single-stranded overhangs. Recently, such overhangs, or TG1-3 tails, were shown to occur on both telomeres of replicated linear plasmids in yeast. Moreover, indirect evidence suggested that the TG1-3 tails also occurred in a yeast strain lacking telomerase. We report herein a novel in-gel hybridization technique to probe telomeres for single-stranded DNA. Using this method, it is shown directly that in yeast strains lacking the TLC1 gene encoding the yeast telomerase RNA, TG1-3 single-stranded DNA was generated on chromosomal and plasmid telomeres. The single-stranded DNA only appeared in S phase and was sensitive to digestion with a single-strand-specific exonuclease. These data demonstrate that during replication of telomeres, TG1-3 tails can be generated in a way that is independent of telomerase-mediated strand elongation. In wild-type strains, these TG1-3 tails could subsequently serve as substrates for telomerase and telomere binding proteins on all telomeres.

摘要

当前的端粒复制模型预测,由于参与线性DNA半保留复制的聚合酶的特性,两个子代分子有一端是平端,另一端有一个短的3'端突出。端粒酶被认为可以延长短的3'端突出以产生长的单链突出。最近,在酵母中复制的线性质粒的两个端粒上都发现了这种突出,即TG1-3尾。此外,间接证据表明TG1-3尾也出现在缺乏端粒酶的酵母菌株中。我们在此报告一种用于探测端粒单链DNA的新型凝胶内杂交技术。使用这种方法,直接表明在缺乏编码酵母端粒酶RNA的TLC1基因的酵母菌株中,染色体和质粒端粒上产生了TG1-3单链DNA。单链DNA仅出现在S期,并且对单链特异性核酸外切酶的消化敏感。这些数据表明,在端粒复制过程中,TG1-3尾可以以独立于端粒酶介导的链延长的方式产生。在野生型菌株中,这些TG1-3尾随后可以作为所有端粒上的端粒酶和端粒结合蛋白的底物。

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