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人DNA聚合酶η对环境致癌物N-(2'-脱氧鸟苷-8-基)-3-氨基苯并蒽加合物的无错绕过机制

Mechanism of Error-Free Bypass of the Environmental Carcinogen N-(2'-Deoxyguanosin-8-yl)-3-aminobenzanthrone Adduct by Human DNA Polymerase η.

作者信息

Patra Amritraj, Politica Dustin A, Chatterjee Arindom, Tokarsky E John, Suo Zucai, Basu Ashis K, Stone Michael P, Egli Martin

机构信息

Department of Biochemistry, Vanderbilt University, School of Medicine, 868A Robinson Research Building, Nashville, TN, 37232, USA.

Department of Chemistry, Vanderbilt University, College of Arts & Science, Station B, Box 1822, Nashville, TN, 37235, USA.

出版信息

Chembiochem. 2016 Nov 3;17(21):2033-2037. doi: 10.1002/cbic.201600420. Epub 2016 Sep 13.

Abstract

The environmental pollutant 3-nitrobenzanthrone produces bulky aminobenzanthrone (ABA) DNA adducts with both guanine and adenine nucleobases. A major product occurs at the C8 position of guanine (C8-dG-ABA). These adducts present a strong block to replicative polymerases but, remarkably, can be bypassed in a largely error-free manner by the human Y-family polymerase η (hPol η). Here, we report the crystal structure of a ternary Pol⋅DNA⋅dCTP complex between a C8-dG-ABA-containing template:primer duplex and hPol η. The complex was captured at the insertion stage and provides crucial insight into the mechanism of error-free bypass of this bulky lesion. Specifically, bypass involves accommodation of the ABA moiety inside a hydrophobic cleft to the side of the enzyme active site and formation of an intra-nucleotide hydrogen bond between the phosphate and ABA amino moiety, allowing the adducted guanine to form a standard Watson-Crick pair with the incoming dCTP.

摘要

环境污染物3-硝基苯并蒽酮会与鸟嘌呤和腺嘌呤碱基形成大体积的氨基苯并蒽酮(ABA)DNA加合物。一种主要产物出现在鸟嘌呤的C8位置(C8-dG-ABA)。这些加合物对复制性聚合酶有很强的阻碍作用,但值得注意的是,人类Y家族聚合酶η(hPol η)能以基本无差错的方式绕过它们。在此,我们报告了含C8-dG-ABA的模板:引物双链体与hPol η之间三元Pol·DNA·dCTP复合物的晶体结构。该复合物在插入阶段被捕获,为这种大体积损伤的无差错绕过机制提供了关键见解。具体而言,绕过过程包括将ABA部分容纳在酶活性位点一侧的疏水裂缝中,并在磷酸基团和ABA氨基部分之间形成核苷酸内氢键,使加合的鸟嘌呤与进入的dCTP形成标准的沃森-克里克碱基对。

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