The Chinese hamster V79 cell mutant V-H4 is phenotypically like Fanconi anemia cells
- 1 November 1990
- journal article
- Published by Springer Nature in Somatic Cell and Molecular Genetics
- Vol. 16 (6) , 575-581
- https://doi.org/10.1007/bf01233098
Abstract
It has been shown by genetic complementation analysis that a mitomycin C-sensitive mutant (V-H4) of Chinese hamster V79 cells is the first rodent equivalent of Fanconi anemia (FA) group A. The V-H4 mutant shows many typical characteristics of cells derived from FA patients. V-H4 cells exhibit increased sensitivity towards cross-linking agents as MMC (∼30-fold), cis-DDP (∼10-fold), DEB (∼10-fold), and PUVA (∼1.6-fold), but an only slightly increased sensitivity to monofunctional alkylating agents (EMS and MMS) and actinomycin D. V-H4 cells are also moderately sensitive to adriamycin (1.6-fold), and not sensitive to H2O2. The levels of chromosomal aberrations induced by MMC and cis-DDP treatment are higher (4- to 6-fold) in V-H4 cells than in the wild-type V79 cells. Genetic complementation analysis with other Chinese hamster mutants hypersensitive to MMC (irs1, irs1SF, UV20 and UV41) indicates clearly that V-H4 belongs to a different, new complementation group. This unique mutant is very stable and can serve as a vehicle to isolate the complementing FA-A gene from normal human DNA.Keywords
This publication has 20 references indexed in Scilit:
- Biochemical and genetic analysis of the Chinese hamster mutants irs1 and irs2 and their comparison to cultured ataxia telangiectasia cellsMutagenesis, 1990
- Chromosomal hypersensitivity in mutant MCN-151 mouse cells exposed to mitomycin CMutation Research Letters, 1989
- Mutagen-sensitive cell lines are obtained with high frequency in V79 Chinese cellsMutation Research - Fundamental and Molecular Mechanisms of Mutagenesis, 1987
- Molecular cloning of a human DNA repair geneNature, 1984
- Isolation and characterization of mitomycin-C-sensitive mouse lymphoma cell mutantsMutation Research - Fundamental and Molecular Mechanisms of Mutagenesis, 1983
- Genetically determined chromosome instability syndromesCytogenetic and Genome Research, 1982
- Specific cellular defects in patients with Fanconi anemiaJournal of Cellular Physiology, 1979
- Cross-link repair in human cells and its possible defect in Fanconi's anemia cellsJournal of Molecular Biology, 1977
- Growth of cultured cells from patients with Fanconi anemiaJournal of Cellular Physiology, 1976
- Is Fanconi's anaemia defective in a process essential to the repair of DNA cross links?Nature, 1975