Previous Article | Next Article ![]()
Journal of Bacteriology, March 1999, p. 1576-1584, Vol. 181, No. 5
Department of Microbiology and Molecular
Genetics and The Molecular Biology Institute, University of
California, Los Angeles, California 90095
Received 28 August 1998/Accepted 8 December 1998
We have constructed strains that allow a direct selection for
mutators of Escherichia coli on a single plate medium. The
plate selection is based on using two different markers whose reversion is enhanced by a given mutator. Plates containing limiting amounts of
each respective nutrient allow the growth of ghost colonies or
microcolonies that give rise to full-size colonies only if a reversion
event occurs. Because two successive mutational events are required,
mutator cells are favored to generate full-size colonies. Reversion of
a third marker allows direct visualization of the mutator phenotype by
the large number of blue papillae in the full-size colonies. We also
describe plate selections involving three successive nutrient markers
followed by a fourth papillation step. Different frameshift or base
substitution mutations are used to select for mismatch-repair-defective
strains (mutHLS and uvrD). We can detect and
monitor mutator cells arising spontaneously, at frequencies lower than
10
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Direct Selection for Mutators in
Escherichia coli
5 in the population. Also, we can measure a mutator
cascade, in which one type of mutator (mutT) generates a
second mutator (mutHLS) that then allows stepwise
frameshift mutations. We discuss the relevance of mutators arising on a
single medium as a result of cells overcoming successive growth
barriers to the development and progression of cancerous tumors, some
of which are mutator cell lines.
*
Corresponding author. Mailing address: Department of
Microbiology and Molecular Genetics and The Molecular Biology
Institute, University of California, Los Angeles, CA 90095. Phone:
(310) 825-8460. Fax: (310) 206-3088. E-mail:
jhmiller{at}mbi.ucla.edu.
This article has been cited by other articles:
| Appl. Environ. Microbiol. | Infect. Immun. | Eukaryot. Cell |
|---|---|---|
| Mol. Cell. Biol. | J. Virol. | Microbiol. Mol. Biol. Rev. |
| ALL ASM JOURNALS |