首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >Pulsed-field gel electrophoresis analysis of the repair of psoralen plus UVA induced DNA photoadducts in Saccharomyces cerevisiae.
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Pulsed-field gel electrophoresis analysis of the repair of psoralen plus UVA induced DNA photoadducts in Saccharomyces cerevisiae.

机译:补骨脂加UVA诱导的酿酒酵母DNA光加合物修复的脉冲场凝胶电泳分析。

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摘要

In the yeast Saccharomyces cerevisiae, double-strand breaks (DSB) have been observed during the DNA repair of psoralen plus UVA induced lesions. In the present paper, we analyzed this repair step in some detail using pulsed-field gel electrophoresis (CHEF) to get a better understanding of this phenomenon with regard to the type of lesions induced and the repair pathways involved. The results confirm that, during post-treatment incubation of Saccharomyces cerevisiae cells, DSB are formed. Their appearance is dose-dependent and the rate of induction is comparable in large (chromosome IV) and small (chromosome III) chromosomes. The formation of DSB is evidenced by the breakage of linear chromosomes III and IV, but also, after high doses, by the linearization of a circular form of chromosome III. The induction of DSB appears to be highly dependent on the induction of interstrand cross-links since they are clearly present after treatments with 8-MOP plus 365 nm radiation (inducing monoadducts and cross-linking in DNA), but practically absent after treatment with 8-MOP plus 405 nm radiation (inducing predominantly monoadducts) at comparable levels of photoadducts. The occurrence of DSB is dependent on the RAD2 and RAD52, but not on the RAD6 gene. It is likely that the specific processing of DNA lesions involving DSB is related to the genotoxic consequences observed.
机译:在酵母酿酒酵母中,在补骨脂素和UVA诱导的损伤的DNA修复过程中已观察到双链断裂(DSB)。在本文中,我们使用脉冲场凝胶电泳(CHEF)对这一修复步骤进行了详细分析,以更好地了解这种现象,包括引起的病变类型和涉及的修复途径。结果证实,在酿酒酵母细胞的处理后孵育期间,形成了DSB。它们的出现是剂量依赖性的,并且诱导率在大(IV型染色体)和小(III型染色体)中相当。 DSB的形成可以通过线性染色体III和IV的断裂来证明,也可以在高剂量后通过圆形染色体III的线性化来证明。 DSB的诱导似乎高度依赖于链间交联的诱导,因为它们在经过8-MOP加365 nm辐射处理后明显存在(诱导DNA中的单加合物和交联),但在用8 MOP处理后几乎不存在。 -MOP加405 nm辐射(主要诱导单加合物),且光加合物的水平相当。 DSB的出现取决于RAD2和RAD52,而不取决于RAD6基因。涉及DSB的DNA损伤的具体处理可能与观察到的遗传毒性后果有关。

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