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光诱导吉尔vocarcin V及其苷元对DNA的修饰作用。

Light-induced modifications of DNA by gilvocarcin V and its aglycone.

作者信息

Tse-Dinh Y C, McGee L R

出版信息

Biochem Biophys Res Commun. 1987 Mar 30;143(3):808-12. doi: 10.1016/0006-291x(87)90320-2.

Abstract

Gilvocarcins are antitumor agents that have been reported to damage DNA upon activation by visible light. This activation is dependent on interaction with DNA. Here it is shown that gilvocarcin V and its synthetic aglycone analogue can both introduce single-strand scission into plasmid DNA. Light irradiation is required for the reaction. The binding of gilvocarcin V to plasmid DNA in the absence of light decreased the DNA linking number in a fashion similar to known intercalating agents such as ethidium bromide. The use of oligonucleotides as substrates for gilvocarcin V demonstrated that one of the steps of the reaction following binding of gilvocarcin V to DNA involves covalent modification at thymidine and to a lesser extent, cytosine residues.

摘要

吉尔vocarcin是一类抗肿瘤药物,据报道,其在可见光激活后会损伤DNA。这种激活依赖于与DNA的相互作用。本文表明,吉尔vocarcin V及其合成苷元类似物均可使质粒DNA产生单链断裂。该反应需要光照。在无光条件下,吉尔vocarcin V与质粒DNA的结合以类似于已知嵌入剂(如溴化乙锭)的方式降低了DNA的连环数。以寡核苷酸作为吉尔vocarcin V的底物表明,吉尔vocarcin V与DNA结合后反应的其中一个步骤涉及对胸腺嘧啶核苷的共价修饰,对胞嘧啶残基的修饰程度较小。

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