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首页> 外文期刊>Genetics: A Periodical Record of Investigations Bearing on Heredity and Variation >Marker-dependent recombination in T4 bacteriophage. IV. Recombinational effects of antimutator T4 DNA polymerase.
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Marker-dependent recombination in T4 bacteriophage. IV. Recombinational effects of antimutator T4 DNA polymerase.

机译:T4噬菌体中的标记依赖性重组。 IV。抗突变体T4 DNA聚合酶的重组作用。

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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.
机译:在rIIB突变体之间的杂交中研究了编码DNA聚合酶的噬菌体T4基因43的抗突变体等位基因tsL42的重组作用。 tsL42限制条件下的重组与正常情况在几个方面有所不同:(1)基本重组得到增强,尤其是在很短的距离内; (2)错配修复的时间缩短了,而错配修复对重组的贡献没有改变; (3)极短距离的标记干扰增加了。我们推断,T4 DNA聚合酶直接参与错配修复,既切除不匹配的单链(通过其3'-> 5'核酸外切酶),又填补了产生的缺口。错配修复的途径得到证实;它包括内切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,很短距离的标记干扰可能是由重组中间体的最终加工过程中相同的事件序列引起的。

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