CHARACTERISTICS OF UV-INDUCED MUTATION SPECTRA IN HUMAN XP-D/ERCC2 GENE-MUTATED XERODERMA-PIGMENTOSUM AND TRICHOTHIODYSTROPHY CELLS

被引:32
作者
MARIONNET, C
BENOIT, A
BENHAMOU, S
SARASIN, A
STARY, A
机构
[1] INST RECH SCI CANC,IFC1,MOLEC GENET LAB,CNRS,UPR 42,F-94801 VILLEJUIF,FRANCE
[2] INST GUSTAVE ROUSSY,INSERM,U351,CANC EPIDEMIOL UNIT,F-94805 VILLEJUIF,FRANCE
关键词
DNA REPAIR; UV MUTAGENESIS; SHUTTLE VECTOR; XERODERMA PIGMENTOSUM; TRICHOTHIODYSTROPHY;
D O I
10.1006/jmbi.1995.0519
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To study the relationships between mutagenesis and carcinogenesis, we compared the mutations and their frequency induced by ultraviolet irradiation at 254 nm (UV-C) in XP-D (GM-08207B/XP6BE), TTD/XP-D (TTD1VI-LAS-KMT11) and wild-type (MRC-5V1) human cells. XP-D and TTD/XP-D cells, mutated in the same XP-D/ERCC2 gene, are deficient in nucleotide excision repair. Whereas XP-D patients develop early skin tumors, TTD patients do not exhibit abnormal levels of cancers. After verification of UV hypersensitivity and DNA repair defect of the immortalized cell lines XP-D and TTD compared with a wild-type cell line, UV-induced mutagenesis was studied with a new shuttle vector pR2, carrying the target lacZ' gene. The UV-mutation frequencies in XP-D and TTD cells were similar and significantly increased compared with normal cells. Sequence analysis of 312 independent mutant plasmids revealed that more rearrangements were induced in TTD cells (16%) than in XP-D (5%) and normal cells (1%), while XP-D cells exhibited a twofold higher rate of tandem mutations compared with TTD and normal cells. In the three cell lines, a predominance of G:C to A:T transitions was found, especially in XP-D cells (87%) and most mutations were targeted on dipyrimidine sites, chiefly on the cytosine at 5'-TC-3' sites. The types of UV-induced point mutations in TTD cells were, however, more similar to those in normal cells than those found in XP-D cells. XP-D mutations were preferentially located in 5'-TCPur-3' sites, while mutations in normal and TTD cells were mostly at 5'-TCC3' sites. Analysis of mutation spectra revealed differences in the location of the mutational hotspots between the three lines. Although the mutation frequency of the UV-irradiated pR2 vector is much higher in TTD and XP-D cells than in normal cells, the mutation spectrum is closer between TTD and normal cells as compared with XP-D cells. These dissimilarities could contribute to an explanation of some of the differences between the two syndromes. (C) 1995 Academic Press Limited
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页码:550 / 562
页数:13
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