Abstract
The main function of vacuolar H(+)-ATPases in eukaryotic cells is to generate proton and electrochemical gradients across the membranes of the vacuolar system. The enzyme is composed of a catalytic sector with five subunits (A-E) and a membrane sector containing at least two subunits (a and c). We disrupted two genes of this enzyme, in yeast cells, one encoding a subunit of the membrane sector (subunit c) and another encoding a subunit of the catalytic sector (subunit B). The resulting mutants did not grow in medium with a pH value higher than 6.5 and grew well only within a narrow pH range around 5.5. Transformation of the mutants with plasmids containing the corresponding genes repaired the mutations. Thus failure to lower the pH in the vacuolar system of yeast, and probably other eukaryotic cells, is lethal and the mutants may survive only if a low external pH allows for this acidification by fluid-phase endocytosis.
MeSH Terms
Cloning, Molecular
Genes, Fungal
Genes, Lethal
Macromolecular Substances
Models, Biological
Molecular Weight
Mutation
Proton-Translocating ATPases/genetics
Restriction Mapping
Saccharomyces cerevisiae/enzymology,genetics,growth & development
Vacuoles/enzymology
Chemicals
Macromolecular Substances
Proton-Translocating ATPases
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Nelson H
Roche Institute of Molecular Biology, Roche Research Center, Nutley, NJ 07110.
Nelson N
References (28)
28 references, click to expand
-
Gene dosage-dependent secretion of yeast vacuolar carboxypeptidase Y.
J Cell Biol. 1986 May;102(5):1551-7
PMID: 3517002
-
Dissection of a single round of vesicular transport: sequential intermediates for intercisternal movement in the Golgi stack.
Cell. 1989 Feb 10;56(3):357-68
PMID: 2536591
-
A conserved gene encoding the 57-kDa subunit of the yeast vacuolar H+-ATPase.
J Biol Chem. 1989 Jan 25;264(3):1775-8
PMID: 2521486
-
Bafilomycins: a class of inhibitors of membrane ATPases from microorganisms, animal cells, and plant cells.
Proc Natl Acad Sci U S A. 1988 Nov;85(21):7972-6
PMID: 2973058
-
Lysosomal H+-translocating ATPase has a similar subunit structure to chromaffin granule H+-ATPase complex.
Biochim Biophys Acta. 1989 Apr 14;980(2):241-7
PMID: 2522796
-
Mutational analysis of the mitochondrial Rieske iron-sulfur protein of Saccharomyces cerevisiae. I. Construction of a RIP1 deletion strain and isolation of temperature-sensitive mutants.
J Biol Chem. 1989 Mar 5;264(7):3713-22
PMID: 2645276
-
Cold inactivation of vacuolar proton-ATPases.
J Biol Chem. 1989 Feb 25;264(6):3577-82
PMID: 2521638
-
Structure and function of proton translocating ATPase in plasma membranes of plants and fungi.
Biochim Biophys Acta. 1988 Feb 24;947(1):1-28
PMID: 2894226
-
The evolution of H+-ATPases.
Trends Biochem Sci. 1989 Mar;14(3):113-6
PMID: 2524915
-
Properties of H+-translocating adenosine triphosphatase in vacuolar membranes of SAccharomyces cerevisiae.
J Biol Chem. 1981 Nov 10;256(21):10859-63
PMID: 6116710
-
The membrane-associated ATPase from Sulfolobus acidocaldarius is distantly related to F1-ATPase as assessed from the primary structure of its alpha-subunit.
J Biol Chem. 1988 May 5;263(13):6012-5
PMID: 2896191
-
A hitchhiker's guide to analysis of the secretory pathway in yeast.
Methods Cell Biol. 1989;32:3-36
PMID: 2691854
-
H+-ATPases from mitochondria, plasma membranes, and vacuoles of fungal cells.
J Membr Biol. 1986;94(2):83-97
PMID: 2882028
-
Acidification of the endocytic and exocytic pathways.
Annu Rev Biochem. 1986;55:663-700
PMID: 2874766
-
Proton-translocating ATPases.
Annu Rev Cell Biol. 1986;2:179-99
PMID: 2435311
-
Structure, molecular genetics, and evolution of vacuolar H+-ATPases.
J Bioenerg Biomembr. 1989 Oct;21(5):553-71
PMID: 2531737
-
The progenitor of ATP synthases was closely related to the current vacuolar H+-ATPase.
FEBS Lett. 1989 Apr 10;247(1):147-53
PMID: 2540044
-
Endocytosis in yeast: several of the yeast secretory mutants are defective in endocytosis.
Cell. 1985 Apr;40(4):1001-9
PMID: 3886157
-
Intervacuole exchange in the yeast zygote: a new pathway in organelle communication.
Science. 1988 Jul 29;241(4865):589-91
PMID: 3041591
-
Purification and properties of H+-translocating, Mg2+-adenosine triphosphatase from vacuolar membranes of Saccharomyces cerevisiae.
J Biol Chem. 1985 Jan 25;260(2):1090-5
PMID: 2857169
-
Protein targeting to the yeast vacuole.
Trends Biochem Sci. 1989 Aug;14(8):347-50
PMID: 2529676
-
Structure, Function, and Evolution of Proton-ATPases.
Plant Physiol. 1988 Jan;86(1):1-3
PMID: 16665845
-
Pulse labeling of yeast cells and spheroplasts.
Methods Enzymol. 1983;97:324-9
PMID: 6361474
-
Identification of 23 complementation groups required for post-translational events in the yeast secretory pathway.
Cell. 1980 Aug;21(1):205-15
PMID: 6996832
-
Active transport of basic amino acids driven by a proton motive force in vacuolar membrane vesicles of Saccharomyces cerevisiae.
J Biol Chem. 1981 Mar 10;256(5):2079-82
PMID: 6450764
-
Organelle assembly in yeast: characterization of yeast mutants defective in vacuolar biogenesis and protein sorting.
J Cell Biol. 1988 Oct;107(4):1369-83
PMID: 3049619
-
Assay of vacuolar pH in yeast and identification of acidification-defective mutants.
Proc Natl Acad Sci U S A. 1989 Sep;86(18):7027-31
PMID: 2674942
-
Transformation of intact yeast cells treated with alkali cations.
J Bacteriol. 1983 Jan;153(1):163-8
PMID: 6336730