A CHO mutant, UV40, that is sensitive to diverse mutagens and represents a new complementation group of mitomycin C sensitivity

被引:28
作者
Busch, DB
Zdzienicka, MZ
Natarajan, AT
Jones, NJ
Overkamp, WJI
Collins, A
Mitchell, DL
Stefanini, M
Botta, E
Albert, RB
Liu, N
White, DA
vanGool, AJ
Thompson, LH
机构
[1] LEIDEN UNIV, DEPT GENET RADIAT GENET & CHEM MUTAGENESIS, NL-2300 RA LEIDEN, NETHERLANDS
[2] LEIDEN UNIV, JA COHEN INST, NL-2300 RA LEIDEN, NETHERLANDS
[3] UNIV LIVERPOOL, SCH LIFE SCI, DONNAN LABS, DEPT GENET & MICROBIOL, LIVERPOOL L69 3BX, MERSEYSIDE, ENGLAND
[4] ROWETT RES INST, BUCKSBURN AB2 9SB, ABERDEEN, SCOTLAND
[5] UNIV ABERDEEN, BOYD ORR RES CTR, BUCKSBURN AB2 9SB, ABERDEEN, SCOTLAND
[6] UNIV TEXAS, MD ANDERSON CANC CTR, DIV SCI PK RES, SMITHVILLE, TX 78957 USA
[7] CNR, IST GENET BIOCHIM & EVOLUZIONIST, I-27100 PAVIA, ITALY
[8] LAWRENCE LIVERMORE NATL LAB, DIV BIOMED SCI, LIVERMORE, CA 94550 USA
[9] ERASMUS UNIV ROTTERDAM, DEPT CELL BIOL & GENET, NL-3000 DR ROTTERDAM, NETHERLANDS
来源
MUTATION RESEARCH-DNA REPAIR | 1996年 / 363卷 / 03期
关键词
DNA repair; Fanconi's anemia; mitomycin C; mutants; rodent; ultraviolet light;
D O I
10.1016/0921-8777(96)00014-6
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
A new mitomycin C (MMC)-sensitive rodent line, UV40, has been identified in the collection of ultraviolet light-(UV-) sensitive mutants of Chinese hamster ovary (CHO) cells isolated at the previous Facility for Automated Experiments in Cell Biology (FAECB). It was isolated from an UV mutant hunt using mutagenesis of AA8 cells with the DNA intercalating frameshift mutagen ICR170. It is complemented by CHO-UV-1, irs1, irs3, irs1SF, MC5, V-C8 and V-H4 with respect to its MMC sensitivity based on cell survival. Despite having approx, 4 x normal UV sensitivity and increased sensitivity to UV inhibition of DNA replication, it has near-normal incision kinetics of UV irradiated DNA, and normal (6-4) photoproducts removal. It also is not hypermutable by UV, and shows near normal levels of UV inhibition of RNA synthesis. UV40 also has approx, 11X, 10x, 5x and 2x AA8 sensitivity to MMC, ethyl methanesulfonate (EMS), methyl methanesulfonate (MMS), and X-rays, respectively. Thus, its defect apparently does not involve nucleotide excision repair but rather another process, possibly in replicating past lesions. The spontaneous chromosomal aberration frequency is elevated to 20% in UV40, and the baseline frequency of sister chromatid exchange is also similar to 4-fold increased. The phenotype of UV40 appears to differ from all other rodent mutants that have so far been described.
引用
收藏
页码:209 / 221
页数:13
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