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酿酒酵母中两种端粒DNA加工反应的表征

Characterization of two telomeric DNA processing reactions in Saccharomyces cerevisiae.

作者信息

Murray A W, Claus T E, Szostak J W

机构信息

Department of Molecular Biology, Massachusetts General Hospital, Boston 02114.

出版信息

Mol Cell Biol. 1988 Nov;8(11):4642-50. doi: 10.1128/mcb.8.11.4642-4650.1988.

Abstract

We have investigated two reactions that occur on telomeric sequences introduced into Saccharomyces cerevisiae cells by transformation. The elongation reaction added repeats of the yeast telomeric sequence C1-3A to telomeric sequences at the end of linear DNA molecules. The reaction worked on the Tetrahymena telomeric sequence C4A2 and also on the simple repeat CA. The reaction was orientation specific: it occurred only when the GT-rich strand ran 5' to 3' towards the end of the molecule. Telomere elongation occurred by non-template-directed DNA synthesis rather than any type of recombination with chromosomal telomeres, because C1-3A repeats could be added to unrelated DNA sequences between the CA-rich repeats and the terminus of the transforming DNA. The elongation reaction was very efficient, and we believe that it was responsible for maintaining an average telomere length despite incomplete replication by template-directed DNA polymerase. The resolution reaction processed a head-to-head inverted repeat of telomeric sequences into two new telomeres at a frequency of 10(-2) per cell division.

摘要

我们研究了通过转化导入酿酒酵母细胞的端粒序列上发生的两种反应。延伸反应在线性DNA分子末端的端粒序列上添加酵母端粒序列C1-3A的重复序列。该反应对四膜虫端粒序列C4A2以及简单重复序列CA也起作用。该反应具有方向特异性:仅当富含GT的链从5'到3'朝向分子末端时才会发生。端粒延伸是通过非模板导向的DNA合成发生的,而不是与染色体端粒进行任何类型的重组,因为C1-3A重复序列可以添加到富含CA的重复序列与转化DNA末端之间的不相关DNA序列上。延伸反应非常高效,并且我们认为它负责维持平均端粒长度,尽管模板导向的DNA聚合酶进行的复制不完全。解析反应以每个细胞分裂10^(-2)的频率将端粒序列的头对头反向重复序列加工成两个新的端粒。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f631/365553/1902f684e69b/molcellb00071-0067-a.jpg

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