Kusewitt D F, Dyble J, Sherburn T E, Ryan S L, Ji J Y
Department of Cell Biology and Physiology, School of Medicine, University of New Mexico, Albuquerque 87131, USA.
Mutat Res. 1998 Mar;407(2):157-68. doi: 10.1016/s0921-8777(98)00004-4.
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.
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。