首页> 美国卫生研究院文献>Nucleic Acids Research >Analysis of cleavage products of DNA repair enzymes and other nucleases. Characterization of an apurinic/apyrimidinic specific endonuclease from mouse plasmacytoma cells.
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Analysis of cleavage products of DNA repair enzymes and other nucleases. Characterization of an apurinic/apyrimidinic specific endonuclease from mouse plasmacytoma cells.

机译:分析DNA修复酶和其他核酸酶的切割产物。小鼠浆细胞瘤细胞中嘌呤/嘧啶二磷酸特异性核酸内切酶的表征。

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摘要

We have developed a strategy by which the nature of phosphodiester bond breaks produced by various DNA-repair endonucleases and also other nucleases, can be characterized. A purified apurinic/apyrimidinic (AP) specific endonuclease from a permanently established mouse plasmacytoma cell-line (MPC-11) has been examined with respect to the exact incision site generated at the baseless site. By the aid of enzymatic treatment with calf intestinal phosphatase, the 3'-phosphatase activity of T4-polynucleotide kinase, chemical modification with piperidine in addition to the Maxam-Gilbert sequencing procedure, followed by separation on a DNA-sequencing gel, the nature of the cleaved phosphodiester bond, both 3' and 5' to the cleavage site, has been established. The AP-specific endonuclease investigated was classified as a class II AP-endonuclease according to the four possible classes of AP-endonuclease with respect to the termini produced. By use of this technique each single damaged and cleaved site can be investigated separately.
机译:我们已经开发出一种策略,通过它可以表征由各种DNA修复内切核酸酶以及其他核酸酶产生的磷酸二酯键断裂的性质。对于从无碱基位点产生的确切切口位点,已经检查了来自永久建立的小鼠浆细胞瘤细胞系(MPC-11)的纯化的嘌呤/嘧啶二烯酸(AP)特异性核酸内切酶。借助小牛肠磷酸酶的酶促处理,T4-多核苷酸激酶的3'-磷酸酶活性,除Maxam-Gilbert测序程序外,还用哌啶进行化学修饰,然后在DNA测序凝胶上分离,已经建立了到裂解位点的3'和5'的裂解的磷酸二酯键。根据所产生的末端的四种可能的AP核酸内切酶类别,将研究的AP特异性核酸内切酶分类为II类AP核酸内切酶。通过使用此技术,可以分别研究每个受损和分裂的位点。

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