Epistatic interactions of deletion mutants in the genes encoding the F-1-ATPase in yeast Saccharomyces cerevisiae

Citation
Lz. Jie et al., Epistatic interactions of deletion mutants in the genes encoding the F-1-ATPase in yeast Saccharomyces cerevisiae, EMBO J, 18(1), 1999, pp. 58-64
Citations number
36
Categorie Soggetti
Molecular Biology & Genetics
Journal title
EMBO JOURNAL
ISSN journal
02614189 → ACNP
Volume
18
Issue
1
Year of publication
1999
Pages
58 - 64
Database
ISI
SICI code
0261-4189(19990104)18:1<58:EIODMI>2.0.ZU;2-M
Abstract
The F-1-ATPase is a multimeric enzyme (alpha(3)beta(3)gamma delta epsilon) primarily responsible for the synthesis of ATP under aerobic conditions. Th e entire coding region of each of the genes was deleted separately in yeast , providing five null mutant strains. Strains with a deletion in the genes encoding alpha-, beta-, gamma- or delta-subunits were unable to grow while the strain with a null mutation in epsilon was able to grow slowly on mediu m containing glycerol as the carbon source, In addition, strains with a nul l mutation in gamma or delta became 100% rho(0)/rho(-) and the strain with the null mutation in gamma grew much more slowly on medium containing gluco se. These additional phenotypes were not observed in strains with the doubl e mutations: Delta alpha Delta gamma, Delta beta Delta gamma, Delta atp11 D elta gamma, Delta alpha Delta delta, Delta beta Delta delta or Delta atp11 Delta delta. These results indicate that epsilon is not an essential compon ent of the ATP synthase and that mutations in the genes encoding the alpha- and beta-subunits and in ATP11 are epistatic to null mutations in the gene s encoding the gamma- and delta-subunits, These data suggest that the prope nsity to form rho(0)/rho(-) mutations in the gamma and delta null deletion mutant stains and the slow growing phenotypes of the null gamma mutant stra in are due to the assembly of F-1 deficient in the corresponding subunit. T hese results have profound implications for the physiology of normal cells.