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古细菌DNA聚合酶中的一种预读功能可检测到促突变模板链尿嘧啶。

A read-ahead function in archaeal DNA polymerases detects promutagenic template-strand uracil.

作者信息

Greagg M A, Fogg M J, Panayotou G, Evans S J, Connolly B A, Pearl L H

机构信息

Department of Biochemistry and Molecular Biology, University College London, Gower Street, London WC1E 6BT, United Kingdom.

出版信息

Proc Natl Acad Sci U S A. 1999 Aug 3;96(16):9045-50. doi: 10.1073/pnas.96.16.9045.

Abstract

Deamination of cytosine to uracil is the most common promutagenic change in DNA, and it is greatly increased at the elevated growth temperatures of hyperthermophilic archaea. If not repaired to cytosine prior to replication, uracil in a template strand directs incorporation of adenine, generating a G.C --> A.U transition mutation in half the progeny. Surprisingly, genomic analysis of archaea has so far failed to reveal any homologues of either of the known families of uracil-DNA glycosylases responsible for initiating the base-excision repair of uracil in DNA, which is otherwise universal. Here we show that DNA polymerases from several hyperthermophilic archaea (including Vent and Pfu) specifically recognize the presence of uracil in a template strand and stall DNA synthesis before mutagenic misincorporation of adenine. A specific template-checking function in a DNA polymerase has not been observed previously, and it may represent the first step in a pathway for the repair of cytosine deamination in archaea.

摘要

胞嘧啶脱氨基变成尿嘧啶是DNA中最常见的促诱变变化,在嗜热古菌生长温度升高时这种变化会大大增加。如果在复制前未修复回胞嘧啶,模板链中的尿嘧啶会指导腺嘌呤的掺入,从而在一半的子代中产生G.C→A.U转换突变。令人惊讶的是,迄今为止对古菌的基因组分析未能揭示负责启动DNA中尿嘧啶碱基切除修复的两个已知尿嘧啶-DNA糖基化酶家族中的任何同源物,而这种修复在其他生物中是普遍存在的。在这里我们表明,来自几种嗜热古菌(包括Vent和Pfu)的DNA聚合酶能特异性识别模板链中尿嘧啶的存在,并在腺嘌呤发生诱变错掺入之前使DNA合成停滞。以前从未观察到DNA聚合酶具有特定的模板检查功能,它可能代表了古菌中胞嘧啶脱氨基修复途径的第一步。

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