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首页> 外文期刊>Journal of the American Chemical Society >Scope and Mechanism of Interstrand Cross-Link Formation by the C4'-Oxidized Abasic Site
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Scope and Mechanism of Interstrand Cross-Link Formation by the C4'-Oxidized Abasic Site

机译:C4'-氧化的碱性位点形成链间交联的范围和机理

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摘要

The C4'-oxidized abasic site (C4-AP) is a commonly formed DNA lesion, which generates two types of interstrand cross-links (ICLs). The kinetically favored cross-link consists of two full length strands and forms reversibly and exclusively with dA. Cross-link formation is attributed to condensation of C4-AP with the N6-amino group of dA. Formation of the thermodynamic ICL involves cleavage of the strand containing C4-AP on the 3'-side of the lesion. The ratios and yields of the ICLs are highly dependent upon the local sequence. Product analysis of enzyme-digested material reveals that the ICL with dA is a cyclic adduct. Formation of the thermodynamically favored cross-link is catalyzed by the surrounding DNA sequence and occurs favorably with dC and dA but not with dG or dT. Mechanistic studies indicate that β-elimination from C4-AP is the rate-limiting step in the formation of the thermodynamic ICL and that the local DNA environment determines the rate constant for this reaction. The efficiency of ICL formation, the stability of the thermodynamic products, and their possible formation in cells (Regelus, P.; et al. Proc. Natl. Acad. Sci. U.S.A. 2007, 104, 14032) suggest that these lesions will be deleterious to the biological system in which they are produced.
机译:C4'氧化的无碱基位点(C4-AP)是一种常见的DNA损伤,会产生两种类型的链间交联(ICL)。动力学上有利的交联由两条全长链组成,可逆地且仅与dA形成。交联的形成归因于C4-AP与dA的N6-氨基的缩合。热力学ICL的形成涉及在病变的3'侧切割含有C4-AP的链。 ICL的比例和产率高度依赖于本地序列。酶消化的物质的产物分析表明,带有dA的ICL是环状加合物。热力学上有利的交联的形成被周围的DNA序列催化,并且在dC和dA中有利地发生,而在dG或dT中则不然。机理研究表明,从C4-AP消除β是形成热力学ICL的限速步骤,并且局部DNA环境决定了该反应的速率常数。 ICL形成的效率,热力学产物的稳定性以及它们在细胞中的可能形成(Regelus,P.等人,Proc。Natl。Acad。Sci。USA 2007,104,14032)表明这些病变将是有害的产生它们的生物系统。

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  • 来源
    《Journal of the American Chemical Society》 |2009年第31期|11132-11139|共8页
  • 作者单位

    Department of Chemistry, Johns Hopkins University, 3400 North Charles Street, Baltimore, Maryland 21218;

    Department of Chemistry, Johns Hopkins University, 3400 North Charles Street, Baltimore, Maryland 21218;

    Biomolecular NMR Center, Johns Hopkins University, 3400 North Charles Street, Baltimore, Maryland 21218;

    Department of Chemistry, Johns Hopkins University, 3400 North Charles Street, Baltimore, Maryland 21218;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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