We have demonstrated that ethyl methane sulfonate (EMS) exposure of single Chinese hamster ovary (CHO) cells will produce colonies mosaic for glucose-6 phosphate dehydrogenase (G6PD) activity and also colonies uniformly lacking in activity (pure mutant). The unstained cells in these mosaic colonies appear in various sectored patterns which are remarkably similar to patterns observed in yeast and bacteria after similar treatments. This is a new phenomenon for a somatic mammalian cell culture system and we propose to investigate the basis of this phenomenon and use it as a tool to study mutagenesis in mammalian cells. Pure mutant clones may be caused by death of the wild-type cell after the first cell division (lethal sectoring) leaving the mutant cell to grow into a colony. This possibility will be investigated by measuring the amount of lethal sectoring occurring at various mutagen doses, and correlating this with the ratio of pure:mosaic colonies occurring at these doses. Pure mutant and certain mosaic colony type may be caused by multiple-mutational events at the G6PD loci. This possibility will be investigated by examining subclones derived from the same mutant colony for differences in G6PD electrophoretic mobility or alterations in enzyme kinetic parameters. The relationship of DNA repair to mosaic phenomenon will be investigated by examining the following sectoring parameters using mutagenic agents which produce different types of DNA damage: 1) change in mosaic:pure mutant ratio with dose, 2) distribution of sector sizes, 3) timing of the mutational fixation event, 4) production of replicating instabilities and 5) lethal sectoring. These parameters will also be examined using various mutagen sensitive and repair defective CHO mutants and also drugs such as caffeine which inhibit DNA repair. The process of mutagenesis has important health implications since current evidence strongly suggests that carcinogenic agents exert their effect through mutagenic reactions with DNA.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Research Project (R01)
Project #
5R01ES002470-06
Application #
3249812
Study Section
Mammalian Genetics Study Section (MGN)
Project Start
1980-07-01
Project End
1987-03-31
Budget Start
1985-07-01
Budget End
1987-03-31
Support Year
6
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Wistar Institute
Department
Type
DUNS #
042250712
City
Philadelphia
State
PA
Country
United States
Zip Code
19104
Stamato, T D; Richardson, E; Perez, M L (1995) UV-light induces delayed mutations in Chinese hamster cells. Mutat Res 328:175-81
Stamato, T; Guerriero, S; Denko, N (1993) Two methods for assaying DNA double-strand break repair in mammalian cells by asymmetric field inversion gel electrophoresis. Radiat Res 133:60-6
Elia, M C; Motyka, L E; Stamato, T D (1991) Electrotransfer of [32P]NAD allows labeling of ADP-ribosylated proteins in intact Chinese hamster ovary cells. Anal Biochem 192:329-33
Giaccia, A J; MacLaren, R A; Denko, N et al. (1990) Increased sensitivity to killing by restriction enzymes in the XR-1 DNA double-strand break repair-deficient mutant. Mutat Res 236:67-76
Stamato, T D; Denko, N (1990) Asymmetric field inversion gel electrophoresis: a new method for detecting DNA double-strand breaks in mammalian cells. Radiat Res 121:196-205
Giaccia, A J; Denko, N; MacLaren, R et al. (1990) Human chromosome 5 complements the DNA double-strand break-repair deficiency and gamma-ray sensitivity of the XR-1 hamster variant. Am J Hum Genet 47:459-69
Giaccia, A J; Richardson, E; Denko, N et al. (1989) Genetic analysis of XR-1 mutation in hamster and human hybrids. Somat Cell Mol Genet 15:71-7
Stamato, T D; Richardson, E; Ianacone, J et al. (1989) Isolation and characterization of glucose-6-phosphate dehydrogenase-deficient Chinese hamster cells derived from pure mutant colonies. Mutagenesis 4:259-64
Denko, N; Giaccia, A; Peters, B et al. (1989) An asymmetric field inversion gel electrophoresis method for the separation of large DNA molecules. Anal Biochem 178:172-6
Stamato, T D; Dipatri, A; Giaccia, A (1988) Cell-cycle-dependent repair of potentially lethal damage in the XR-1 gamma-ray-sensitive Chinese hamster ovary cell. Radiat Res 115:325-33

Showing the most recent 10 out of 16 publications