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大肠杆菌mutD和mutT途径在预防A:T→C:G颠换中的相互作用。

The interaction of the Escherichia coli mutD and mutT pathways in the prevention of A:T-->C:G transversions.

作者信息

Fowler R G, Amutan M V, Isbell R J

机构信息

Department of Biological Sciences, San Jose State University, CA 95192.

出版信息

Mutat Res. 1992 Dec 16;284(2):307-19. doi: 10.1016/0027-5107(92)90015-t.

Abstract

The Escherichia coli mutT mutator allele produces high frequencies of exclusively A:T-->C:G transversions. This is thought to be caused by a failure to prevent or remove A:G mispairs during DNA replication. The mutD5 mutator allele maps to the dnaQ locus which encodes the epsilon subunit of the DNA polymerase III holoenzyme. This subunit provides 3'-->5' exonuclease, proofreading, activity for removing mispaired nucleotides at the 3' end of the newly synthesized DNA strand. mutD5 has an altered epsilon resulting in reduced levels of proofreading and subsequent high mutation frequencies for all base-pair substitutions. We have analyzed the interaction between mutD5 and mutT-induced A:T-->C:G transversions by measuring reversion frequencies in mutD5 and mutT single mutator strains and mutD5mutT double mutator strains using the well-characterized trpA58 and trpA88 alleles. We find that the double mutator strains produce more A:T-->C:G substitutions than would be expected from simple additivity of the single mutator strains. We interpret this to mean that the two systems, at least in part, do act together to prevent the same mutational intermediate from producing A:T-->C:G transversions. It is estimated that over 90% of the mutT-induced A:G mispairs are corrected by proofreading at the trpA58 site while only about 30% are corrected at trpA88. Reversion frequencies in the mutD5mutT double mutator strains indicate A:G misincorporations occur about 100 x more frequently at trpA58 than at the trpA88 site. Using these and other data we also provide estimations of the fidelity contributions for mutT editing, proofreading and methyl-directed mismatch repair at the two trpA sites for both transversions and the transition that could be scored. In the case of A:T-->C:G transversions, both mutT editing and proofreading make major contributions in error reduction with mismatch repair playing a small or no role at all. For the A:T-->G:C transition, proofreading and mismatch repair were both important in preventing mutations while no contribution was observed for mutT editing.

摘要

大肠杆菌的mutT突变等位基因会产生高频率的仅A:T到C:G的颠换。这被认为是由于在DNA复制过程中未能阻止或去除A:G错配所致。mutD5突变等位基因定位于dnaQ位点,该位点编码DNA聚合酶III全酶的ε亚基。该亚基提供3'到5'外切核酸酶活性,即校对活性,用于去除新合成DNA链3'端的错配核苷酸。mutD5具有改变的ε亚基,导致校对水平降低,随后所有碱基对替换的突变频率都很高。我们通过使用特征明确的trpA58和trpA88等位基因测量mutD5和mutT单突变菌株以及mutD5mutT双突变菌株中的回复频率,分析了mutD5与mutT诱导的A:T到C:G颠换之间的相互作用。我们发现双突变菌株产生的A:T到C:G替换比单突变菌株简单相加预期的要多。我们将此解释为意味着这两个系统至少部分地共同作用以防止相同的突变中间体产生A:T到C:G颠换。据估计,超过90%的mutT诱导的A:G错配在trpA58位点通过校对得到纠正,而在trpA88位点只有约30%得到纠正。mutD5mutT双突变菌株中的回复频率表明,在trpA58位点A:G错掺入的发生频率比在trpA88位点高约100倍。利用这些和其他数据,我们还提供了在两个trpA位点对于颠换和可计分的转换,mutT编辑、校对和甲基导向错配修复对保真度贡献的估计。在A:T到C:G颠换的情况下,mutT编辑和校对在减少错误方面都起主要作用,错配修复起很小或根本不起作用。对于A:T到G:C转换,校对和错配修复在防止突变方面都很重要,而未观察到mutT编辑有贡献。

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