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首页> 外文期刊>Genetics: A Periodical Record of Investigations Bearing on Heredity and Variation >Escherichia coli Strains (ndk) Lacking Nucleoside Diphosphate Kinase Are Powerful Mutators for Base Substitutions and Frameshifts in Mismatch-Repair-Deficient Strains
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Escherichia coli Strains (ndk) Lacking Nucleoside Diphosphate Kinase Are Powerful Mutators for Base Substitutions and Frameshifts in Mismatch-Repair-Deficient Strains

机译:缺乏核苷二磷酸激酶的大肠杆菌菌株(ndk)是错配修复缺陷菌株中碱基取代和移码的强大突变体。

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Nucleoside diphosphate (NDP) kinase is one of the enzymes that maintains triphosphate pools. Escherichia coli strains ( ndk ) lacking this enzyme have been shown to be modest base substitution mutators, and two members of the human family of NDP kinases act as tumor suppressors. We show here that in E. coli strains lacking NDP kinase high levels of mispairs are generated, but most of these are corrected by the mismatch-repair system. Double mutants that are ndk mutS , lacking both the NDP kinase and mismatch repair, have levels of base substitutions 15-fold higher and levels of certain frameshifts up to 10-fold higher than those of the respective mutations in mutS strains that are NDP kinase proficient. A sequence analysis of the specificity of base substitution mutations generated in ndk and ndk mutS backgrounds as well as other experiments suggests that NDP kinase deficiency stimulates polymerase errors that lead to A:T → G:C transitions and that the editing capacity of cells may be affected, leading to additional uncorrected mispairs and to A:T → T:A transversions.
机译:核苷二磷酸(NDP)激酶是维持三磷酸池的酶之一。缺乏这种酶的大肠杆菌菌株(ndk)已被证明是适度的碱基取代突变体,人类NDP激酶家族的两个成员可作为肿瘤抑制因子。我们在这里显示,在缺少NDP激酶的大肠杆菌菌株中,会产生高水平的错配,但其中大多数已通过错配修复系统得到纠正。缺少NDP激酶和错配修复的ndk mutS双重突变体比NDP激酶熟练的mutS菌株的碱基突变水平高15倍,某些移码水平高10倍。 。对在ndk和ndk mutS背景中产生的碱基取代突变的特异性进行序列分析以及其他实验表明,NDP激酶缺乏会刺激聚合酶错误,导致A:T→G:C转换,并且细胞的编辑能力可能是受影响,导致其他未纠正的错误配对,并导致A:T→T:A转换。

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