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大肠杆菌dnaQ和mutD突变体的结构与功能

Structure and function of dnaQ and mutD mutators of Escherichia coli.

作者信息

Takano K, Nakabeppu Y, Maki H, Horiuchi T, Sekiguchi M

出版信息

Mol Gen Genet. 1986 Oct;205(1):9-13. doi: 10.1007/BF02428026.

Abstract

The nucleotide sequences of the recessive dnaQ49 and the dominant mutD5 mutator were determined. The dnaQ49 mutator has a single base substitution in the dnaQ gene, thus causing one amino acid change, 96Val (GTG)----Gly (GGG), in the DnaQ protein (epsilon subunit of DNA polymerase III holoenzyme). The mutD5 mutator possesses two base substitutions in the same gene, resulting in two amino acid changes, 73Leu (TTG)----Trp (TGG) and 164Ala (GCA)----Val (GTA), which were designated the mutD52 and mutD51 mutations, respectively. Construction of chimaeric genes carrying one or two of these mutations revealed: either mutD51 or mutD52 alone causes the dominant mutator phenotype when present in a multi-copy plasmid; mutator phenotype when present in a low-copy plasmid; the dominant mutD51 mutator activity is suppressed by the dnaQ49 mutation when both mutations are present in the same gene. Based on these findings, we devised a model for the action of these mutators.

摘要

测定了隐性dnaQ49和显性mutD5突变体的核苷酸序列。dnaQ49突变体在dnaQ基因中有一个单碱基替换,从而导致DnaQ蛋白(DNA聚合酶III全酶的ε亚基)中的一个氨基酸变化,即96位缬氨酸(GTG)变为甘氨酸(GGG)。mutD5突变体在同一基因中有两个碱基替换,导致两个氨基酸变化,分别为73位亮氨酸(TTG)变为色氨酸(TGG)以及164位丙氨酸(GCA)变为缬氨酸(GTA),这两个变化分别被命名为mutD52和mutD51突变。携带这些突变中的一个或两个的嵌合基因构建结果显示:当mutD51或mutD52单独存在于多拷贝质粒中时会导致显性突变体表型;当存在于低拷贝质粒中时会导致突变体表型;当两个突变存在于同一基因中时,显性的mutD51突变体活性会被dnaQ49突变所抑制。基于这些发现,我们设计了一个这些突变体作用的模型。

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