Bacteriophage T4 rnh (RNase H) null mutations: Effects on spontaneous mutation and epistatic interaction with rII mutations

Citation
A. Bebenek et al., Bacteriophage T4 rnh (RNase H) null mutations: Effects on spontaneous mutation and epistatic interaction with rII mutations, J BACT, 181(10), 1999, pp. 3123-3128
Citations number
32
Categorie Soggetti
Microbiology
Journal title
JOURNAL OF BACTERIOLOGY
ISSN journal
00219193 → ACNP
Volume
181
Issue
10
Year of publication
1999
Pages
3123 - 3128
Database
ISI
SICI code
0021-9193(199905)181:10<3123:BTR(HN>2.0.ZU;2-H
Abstract
The bacteriophage T4 mh gene encodes T4 RNase H, a relative of a family of flap endonucleases. T4 mh null mutations reduce burst sizes, increase sensi tivity to DNA damage, and increase the frequency of acriflavin resistance ( Ac-r) mutations. Because mutations in the related Saccharomyces cerevisiae RAD27 gene display a remarkable duplication mutator phenotype, we further e xplored the impact of mh mutations upon the mutation process. We observed t hat most Ac-r mutants in an rnh(+) strain contain ac mutations, whereas onl y roughly half of the Ac-r mutants detected in an rnh Delta strain bear ac mutations. In contrast to the mutational specificity displayed by most muta tors, the DNA alterations of ac mutations arising in rnh Delta and rnh(+) b ackgrounds are indistinguishable. Thus, the increase in Ac-r mutants in an rnh Delta background is probably not due to a mutator effect. This conclusi on is supported by the lack of increase in the frequency of rI mutations in an rnh Delta background. In a screen that detects mutations at both the rI locus and the much larger rII locus, the r frequency was severalfold lower in an rnh Delta background. This decrease was due to the phenotype of mh r II double mutants, which display an r(+) plaque morphology but retain the c haracteristic inability of rII mutants to grow on lambda lysogens. Finally, we summarize those aspects of T4 forward-mutation systems which are releva nt to optimal choices for investigating quantitative and qualitative aspect s of the mutation process.