α and β subunits of F1-ATPase are required for survival of petite mutants in Saccharomyces cerevisiae

被引:41
作者
Chen, XJ [1 ]
Clark-Walker, GD [1 ]
机构
[1] Australian Natl Univ, Res Sch Biol Sci, Mol & Cellular Genet Grp, Canberra, ACT 2601, Australia
来源
MOLECULAR AND GENERAL GENETICS | 1999年 / 262卷 / 4-5期
关键词
F-1-ATPase; mitochondrial DNA; petite mutation; rho(o) lethality; yeast;
D O I
10.1007/s004380051156
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Although Saccharomyces,ces cerevisiae can form petite mutants with deletions in mitochondrial DNA (mtDNA) (p(-)) and can survive complete loss of the gaanellar genome (p(o)), the genetic factor(s) that permit(s) survival of p(-) and p(o) mutants remain(s) unknown. In this report we show that a function associated with the F-1-ATPase, which is distinct from its role in energy transduction, is required for the petite-positive phenotype of S. cerevisiae. Inactivation of either the alpha or beta subunit, but not the gamma, delta, or epsilon subunit of F-1, renders cells petite-negative. The F-1 complex, or a subcomplex composed of the alpha and beta subunits only, is essential for survival of p(o) cells and those impaired in electron transport. The activity of F1 that suppresses p(o) lethality is independent of the membrane F-o complex, but is associated with an intrinsic ATPase activity. A further demonstration of the ability of F-1 subunits to suppress p(o) lethality has been achieved by simultaneous expression of S. cerevisiae F-1 alpha and gamma subunit genes in Kluyveromyces lactis - which allows this petite-negative yeast to survive the loss of its mtDNA. Consequently, ATP1 and ATP2, in addition to the previously identified AAC2, YME1 and PELI/PGSI genes, are required for establishment of p(-) or p(o) mutations in S. cerevisiae.
引用
收藏
页码:898 / 908
页数:11
相关论文
共 70 条
[1]  
ACKERMAN SH, 1992, J BIOL CHEM, V267, P7386
[2]   IDENTIFICATION OF 2 NUCLEAR GENES (ATP11, ATP12) REQUIRED FOR ASSEMBLY OF THE YEAST F1-ATPASE [J].
ACKERMAN, SH ;
TZAGOLOFF, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (13) :4986-4990
[3]  
ALCONADA A, 1994, J BIOL CHEM, V269, P13670
[4]  
[Anonymous], NUCLEOCYTOPLASMIC RE
[5]   Yeast mitochondrial F1F0-ATP synthase exists as a dimer:: identification of three dimer-specific subunits [J].
Arnold, I ;
Pfeiffer, K ;
Neupert, W ;
Stuart, RA ;
Schägger, H .
EMBO JOURNAL, 1998, 17 (24) :7170-7178
[6]  
ATTARDI G, 1988, ANNU REV CELL BIOL, V4, P289, DOI 10.1146/annurev.cb.04.110188.001445
[7]   The ATP synthase - A splendid molecular machine [J].
Boyer, PD .
ANNUAL REVIEW OF BIOCHEMISTRY, 1997, 66 :717-749
[8]   Functional F1-ATPase essential in maintaining growth and membrane potential of human mitochondrial DNA-depleted ρ° cells [J].
Buchet, K ;
Godinot, C .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (36) :22983-22989
[9]   INDUCTION OF PETITE MUTATION + INHIBITION OF SYNTHESIS OF RESPIRATORY ENZYMES IN VARIOUS YEASTS [J].
BULDER, CJE .
ANTONIE VAN LEEUWENHOEK JOURNAL OF MICROBIOLOGY AND SEROLOGY, 1964, 30 (01) :1-&
[10]   LETHALITY OF PETITE MUTATION IN PETITE NEGATIVE YEASTS [J].
BULDER, CJE .
ANTONIE VAN LEEUWENHOEK JOURNAL OF MICROBIOLOGY AND SEROLOGY, 1964, 30 (04) :442-&