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ABC核酸外切酶修复N-甲基-N'-硝基-N-亚硝基胍诱导的DNA损伤

Repair of N-methyl-N'-nitro-N-nitrosoguanidine-induced DNA damage by ABC excinuclease.

作者信息

Van Houten B, Sancar A

出版信息

J Bacteriol. 1987 Feb;169(2):540-5. doi: 10.1128/jb.169.2.540-545.1987.

Abstract

Escherichia coli has several overlapping DNA repair pathways which act in concert to eliminate the DNA damage caused by a diverse array of physical and chemical agents. The ABC excinuclease which is encoded by the uvrA, uvrB, and uvrC genes mediates both the incision and excision steps of nucleotide excision repair. Traditionally, this repair pathway has been assumed to be active against DNA adducts that cause major helical distortions. To determine the level of helical deformity required for recognition and repair by ABC excinuclease, we have evaluated the substrate specificity of this enzyme by using DNA damaged by N-methyl-N'-nitro-N-nitrosoguanidine. ABC excinuclease incised methylated DNA in vitro in a dose-dependent manner in a reaction that was ATP dependent and specific for the fully reconstituted enzyme. In vivo studies with various alkylation repair-deficient mutants indicated that the excinuclease participated in the repair of DNA damage induced by N-methyl-N'-nitro-N-nitrosoguanidine.

摘要

大肠杆菌有几种重叠的DNA修复途径,它们协同作用以消除由各种物理和化学因子引起的DNA损伤。由uvrA、uvrB和uvrC基因编码的ABC核酸外切酶介导核苷酸切除修复的切割和切除步骤。传统上,这种修复途径被认为对引起主要螺旋扭曲的DNA加合物具有活性。为了确定ABC核酸外切酶识别和修复所需的螺旋畸形水平,我们通过使用被N-甲基-N'-硝基-N-亚硝基胍损伤的DNA来评估该酶的底物特异性。ABC核酸外切酶在体外以剂量依赖的方式切割甲基化DNA,该反应依赖ATP且对完全重组的酶具有特异性。对各种烷基化修复缺陷突变体的体内研究表明,核酸外切酶参与了由N-甲基-N'-硝基-N-亚硝基胍诱导的DNA损伤的修复。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/660d/211811/660bbee7837e/jbacter00192-0107-a.jpg

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