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T4噬菌体中依赖标记的重组。IV. 抗突变T4 DNA聚合酶的重组效应。

Marker-dependent recombination in T4 bacteriophage. IV. Recombinational effects of antimutator T4 DNA polymerase.

作者信息

Shcherbakov V P, Plugina L A, Kudryashova E A

机构信息

Institute of Chemical Physics in Chernogolovka, Russian Academy of Sciences, Moscow Region.

出版信息

Genetics. 1995 May;140(1):13-25. doi: 10.1093/genetics/140.1.13.

Abstract

Recombinational effects of the antimutator allele tsL42 of gene 43 of phage T4, encoding DNA polymerase, were studied in crosses between rIIB mutants. Recombination under tsL42-restricted conditions differed from the normal one in several respects: (1) basic recombination was enhanced, especially within very short distances; (2) mismatch repair tracts were shortened, while the contribution of mismatch repair to recombination was not changed; (3) marker interference at very short distances was augmented. We infer that the T4 DNA polymerase is directly involved in mismatch repair, performing both excision of a nonmatched single strand (by its 3'-->5' exonuclease) and filling the resulting gap. A pathway for the mismatch repair was substantiated; it includes sequential action of endo VII (gp49)-->3'-->5' exonuclease (gp43)-->DNA polymerase (gp43)-->DNA ligase (gp30). It is argued that the marker interference at very short distances may result from the same sequence of events during the final processing of recombinational intermediates.

摘要

对噬菌体T4编码DNA聚合酶的基因43的抗突变等位基因tsL42的重组效应,在rIIB突变体之间的杂交中进行了研究。在tsL42限制条件下的重组在几个方面与正常重组不同:(1)基本重组增强,特别是在非常短的距离内;(2)错配修复片段缩短,而错配修复对重组的贡献不变;(3)在非常短的距离内标记干扰增加。我们推断T4 DNA聚合酶直接参与错配修复,既通过其3'→5'核酸外切酶切除不匹配的单链,又填充产生的缺口。证实了一条错配修复途径;它包括内切酶VII(gp49)→3'→5'核酸外切酶(gp43)→DNA聚合酶(gp43)→DNA连接酶(gp30)的顺序作用。有人认为,在非常短的距离内的标记干扰可能是由于重组中间体最终加工过程中相同的事件序列导致的。

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Recombination in bacteriophage T4.噬菌体T4中的重组
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The amount of DNA between genetic markers in phage T4.
Proc Natl Acad Sci U S A. 1966 Nov;56(5):1457-63. doi: 10.1073/pnas.56.5.1457.

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