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DNA single-strand break repair and spinocerebellar ataxia.DNA单链断裂修复与脊髓小脑共济失调
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A plant 3'-phosphoesterase involved in the repair of DNA strand breaks generated by oxidative damage.一种参与修复由氧化损伤产生的DNA链断裂的植物3'-磷酸酯酶。
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XRCC1 stimulates human polynucleotide kinase activity at damaged DNA termini and accelerates DNA single-strand break repair.XRCC1在受损DNA末端刺激人多核苷酸激酶活性,并加速DNA单链断裂修复。
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通过聚(ADP-核糖)聚合酶样指状结构感知DNA损伤。

Sensing DNA damage by PARP-like fingers.

作者信息

Petrucco Stefania

机构信息

Department of Biochemistry and Molecular Biology, University of Parma, Parco Area delle Scienze 23/A, I-43100 Parma, Italy.

出版信息

Nucleic Acids Res. 2003 Dec 1;31(23):6689-99. doi: 10.1093/nar/gkg890.

DOI:10.1093/nar/gkg890
PMID:14627802
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC290258/
Abstract

PARP-like zinc fingers are protein modules, initially described as nick-sensors of poly(ADP-ribosyl)-polymerases (PARPs), which are found at the N-terminus of different DNA repair enzymes. I chose to study the role of PARP-like fingers in AtZDP, a 3' DNA phosphoesterase, which is the only known enzyme provided with three such finger domains. Here I show that PARP-like fingers can maintain AtZDP onto damaged DNA sites without interfering with its DNA end repair functions. Damage recognition by AtZDP fingers, in fact, relies on the presence of flexible joints within double-strand DNA and does not entail DNA ends. A single AtZDP finger is already capable of specific recognition. Two fingers strengthen the binding and extend the contacts on the bound DNA. A third finger further enhances the specific binding to damaged DNA sites. Unexpectedly, gaps but not nicks are bound by AtZDP fingers, suggesting that nicks on a naked DNA template do not provide enough flexibility for the recognition. Altogether these results indicate that AtZDP PARP-like fingers, might have a role in positioning the enzyme at sites of enhanced helical flexibility, where single-strand DNA breaks are present or are prone to occur.

摘要

聚(ADP - 核糖)聚合酶(PARP)样锌指是蛋白质模块,最初被描述为聚(ADP - 核糖)聚合酶(PARP)的切口传感器,存在于不同DNA修复酶的N端。我选择研究PARP样锌指在AtZDP(一种3' DNA磷酸二酯酶)中的作用,AtZDP是唯一已知具有三个此类锌指结构域的酶。在此我表明,PARP样锌指可以将AtZDP维持在受损DNA位点上,而不干扰其DNA末端修复功能。事实上,AtZDP锌指对损伤的识别依赖于双链DNA中柔性接头的存在,并不需要DNA末端。单个AtZDP锌指就已经能够进行特异性识别。两个锌指会加强结合并扩展与结合DNA的接触。第三个锌指进一步增强了对受损DNA位点的特异性结合。出乎意料的是,AtZDP锌指结合的是缺口而非切口,这表明裸DNA模板上的切口没有为识别提供足够的灵活性。总之,这些结果表明AtZDP的PARP样锌指可能在将该酶定位到螺旋柔性增强的位点中发挥作用,这些位点存在单链DNA断裂或容易发生单链DNA断裂。