Expression of a mammalian DNA photolyase confers light-dependent repair activity and reduces mutations of UV-irradiated shuttle vectors in xeroderma pigmentosum cells

被引:15
作者
Asahina, H
Han, ZB
Kawanishi, M
Kato, T
Ayaki, H
Todo, T
Yagi, T
Takebe, H
Ikenaga, M
Kimura, SH
机构
[1] Kyoto Univ, Radiat Biol Ctr, Sakyo Ku, Kyoto 6068501, Japan
[2] Kyoto Univ, Dept Environm Qual Control, Shiga 5200811, Japan
[3] Kyoto Univ, Grad Sch Med, Dept Radiat Genet, Sakyo Ku, Kyoto 6068501, Japan
[4] Res Inst Microbial Dis, Dept Mol Genet, Suita, Osaka 565, Japan
来源
MUTATION RESEARCH-DNA REPAIR | 1999年 / 435卷 / 03期
关键词
CPD photolyase; expression of photolyase cDNA; photoreactivation of killing and mutations; Xeroderma pigmentosum (XP) cells; supF gene mutations;
D O I
10.1016/S0921-8777(99)00051-8
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Photoreactivation is one of the DNA repair mechanisms to remove UV lesions from cellular DNA with a function of the DNA photolyase and visible light. Two types of photolyase specific for cyclobutane pyrimidine dimers (CPD) and for pyrimidine (6-4) pyrimidones (6-4PD) are found in nature, but neither is present in cells from placental mammals. To investigate the effect of the CPD-specific photolyase on killing and mutations induced by UV, we expressed a marsupial DNA photolyase in DNA repair-deficient group A xeroderma pigmentosum (XP-A) cells. Expression of the photolyase and visible light irradiation removed CPD from cellular DNA and elevated survival of the UV-irradiated XP-A cells, and also reduced mutation frequencies of UV-irradiated shuttle vector plasmids replicating in XP-A cells. The survival of UV-irradiated cells and mutation frequencies of W-irradiated plasmids were not completely restored to the unirradiated levels by the removal of CPD, These results suggest that both CPD and other UV damage, probably 6-4PD, can lead to cell killing and mutations. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:255 / 262
页数:8
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