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表达核酸内切酶V的修复功能正常的小鼠成纤维细胞中紫外线抗性和紫外线突变谱的改变

Altered UV resistance and UV mutational spectrum in repair-proficient murine fibroblasts expressing endonuclease V.

作者信息

Kusewitt D F, Dyble J, Sherburn T E, Ryan S L, Ji J Y

机构信息

Department of Cell Biology and Physiology, School of Medicine, University of New Mexico, Albuquerque 87131, USA.

出版信息

Mutat Res. 1998 Mar;407(2):157-68. doi: 10.1016/s0921-8777(98)00004-4.

Abstract

In previously reported studies, we transfected repair-proficient murine fibroblasts with the denV gene of bacteriophage T4 and showed that expression of encoded endonuclease V markedly enhanced cyclobutane pyrimidine dimer (CPD) repair and reduced the frequency of ultraviolet radiation (UV)-induced mutations. In the present studies, we compared the spectra of UV-induced mutations at the hprt locus in denV-transfected and control cells. A significant difference in mutation types was observed. While multiple base deletions and single base insertions were found in denV-transfected but not control cells, multiple tandem and non-tandem point mutations identified in control cells were absent in denV-transfected cells. When we compared colony survival following UV exposure in the two cell lines, it appeared that endonuclease V expression did not enhance UV resistance, instead denV-transfected cells had increased susceptibility to low fluences of UV. The effects of endonuclease V expression on UV resistance and on UV mutational spectrum are likely to be due both to the removal of CPDs and to the novel enzymatic activity of endonuclease V.

摘要

在先前报道的研究中,我们用噬菌体T4的denV基因转染了具有修复能力的小鼠成纤维细胞,并表明编码的核酸内切酶V的表达显著增强了环丁烷嘧啶二聚体(CPD)的修复,并降低了紫外线辐射(UV)诱导的突变频率。在本研究中,我们比较了denV转染细胞和对照细胞中hprt基因座处紫外线诱导突变的谱。观察到突变类型存在显著差异。虽然在denV转染细胞中发现了多个碱基缺失和单碱基插入,但在对照细胞中未发现,而在对照细胞中鉴定出的多个串联和非串联点突变在denV转染细胞中不存在。当我们比较两种细胞系紫外线照射后的集落存活率时,似乎核酸内切酶V的表达并未增强紫外线抗性,相反,denV转染细胞对低剂量紫外线的敏感性增加。核酸内切酶V表达对紫外线抗性和紫外线突变谱的影响可能既归因于CPD的去除,也归因于核酸内切酶V的新酶活性。

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