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大肠杆菌 DNA 聚合酶 IV DinB 对胞嘧啶类似物 tC 的歧视。

Discrimination against the cytosine analog tC by Escherichia coli DNA polymerase IV DinB.

机构信息

Department of Chemistry and Chemical Biology, Northeastern University, 360 Huntington Avenue, Boston, MA 02115, USA.

出版信息

J Mol Biol. 2011 Jun 3;409(2):89-100. doi: 10.1016/j.jmb.2011.03.069. Epub 2011 Apr 6.

Abstract

The cytosine analog 1,3-diaza-2-oxophenothiazine (tC) is a fluorescent nucleotide that forms Watson-Crick base pairs with dG. The Klenow fragment of DNA polymerase I (an A-family polymerase) can efficiently bypass tC on the template strand and incorporate deoxyribose-triphosphate-tC into the growing primer terminus. Y-family DNA polymerases are known for their ability to accommodate bulky lesions and modified bases and to replicate beyond such nonstandard DNA structures in a process known as translesion synthesis. We probed the ability of the Escherichia coli Y-family DNA polymerase DinB (Pol IV) to copy DNA containing tC and to incorporate tC into a growing DNA strand. DinB selectively adds dGTP across from tC in template DNA but cannot extend beyond the newly formed G:tC base pair. However, we find that DinB incorporates the tC deoxyribonucleotide triphosphate opposite template G and extends from tC. Therefore, DinB displays asymmetry in terms of its ability to discriminate against the modification of the DNA template compared to the incoming nucleotide. In addition, our finding that DinB (a lesion-bypass DNA polymerase) specifically discriminates against tC in the template strand may suggest that DinB discriminates against template modifications in the major groove of DNA.

摘要

胞嘧啶类似物 1,3-二氮杂-2-氧吩噻嗪(tC)是一种荧光核苷酸,可与 dG 形成 Watson-Crick 碱基对。DNA 聚合酶 I 的 Klenow 片段(A 家族聚合酶)可有效绕过模板链上的 tC,并将脱氧核糖三磷酸-tC 掺入到延伸的引物末端。众所周知,Y 家族 DNA 聚合酶能够容纳大体积的损伤和修饰碱基,并在称为跨损伤合成的过程中复制超过这些非标准 DNA 结构。我们探究了大肠杆菌 Y 家族 DNA 聚合酶 DinB(Pol IV)复制含有 tC 的 DNA 并将 tC 掺入到生长 DNA 链中的能力。DinB 可选择性地在模板 DNA 中的 tC 对面添加 dGTP,但不能延伸到新形成的 G:tC 碱基对之外。然而,我们发现 DinB 在模板 G 处掺入 tC 脱氧核苷酸三磷酸并从 tC 延伸。因此,DinB 在识别 DNA 模板修饰方面的能力相对于进入的核苷酸存在不对称性。此外,我们发现 DinB(一种损伤回避 DNA 聚合酶)在模板链上特异性地识别 tC,这可能表明 DinB 在 DNA 大沟中特异性地识别模板修饰。

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