Literature DB >> 10480897

A novel family of yeast chaperons involved in the distribution of V-ATPase and other membrane proteins.

A Cohen1, N Perzov, H Nelson, N Nelson.   

Abstract

Null mutations in genes encoding V-ATPase subunits in Saccharomyces cerevisiae result in a phenotype that is unable to grow at high pH and is sensitive to high and low metal-ion concentrations. Treatment of these null mutants with ethylmethanesulfonate causes mutations that suppress the V-ATPase null phenotype, and the mutant cells are able to grow at pH 7.5. The suppressor mutants were denoted as svf (suppressor of V-ATPase function). The frequency of svf is relatively high, suggesting a large target containing several genes for the ethylmethanesulfonate mutagenesis. The suppressors' frequency is dependent on the individual genes that were inactivated to manifest the V-ATPase null mutation. The svf mutations are recessive, because crossing the svf mutants with their corresponding V-ATPase null mutants resulted in diploid strains that are unable to grow at pH 7.5. A novel gene family in which null mutations cause pleiotropic effects on metal-ion resistance or sensitivity and distribution of membrane proteins in different targets was discovered. The family was defined as VTC (Vacuolar Transporter Chaperon) and it contains four genes in the S. cerevisiae genome. Inactivation of one of them, VTC1, in the background of V-ATPase null mutations resulted in svf phenotype manifested by growth at pH 7.5. Deletion of the VTC1 gene (DeltaVTC1) results in a reduced amount of V-ATPase in the vacuolar membrane. These mutant cells fail to accumulate quinacrine into their vacuoles, but they are able to grow at pH 7.5. The VTC1 null mutant also results in a reduced amount of the plasma membrane H(+)-ATPase (Pma1p) in membrane preparations and possibly mis-targeting. This observation may provide an explanation for the svf phenotype in the double disruptant mutants of DeltaVTC1 and DeltaVMA subunits.

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Year:  1999        PMID: 10480897     DOI: 10.1074/jbc.274.38.26885

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  35 in total

1.  Rho1p and Cdc42p act after Ypt7p to regulate vacuole docking.

Authors:  G Eitzen; N Thorngren; W Wickner
Journal:  EMBO J       Date:  2001-10-15       Impact factor: 11.598

Review 2.  A journey from mammals to yeast with vacuolar H+-ATPase (V-ATPase).

Authors:  Nathan Nelson
Journal:  J Bioenerg Biomembr       Date:  2003-08       Impact factor: 2.945

3.  TgVTC2 is involved in polyphosphate accumulation in Toxoplasma gondii.

Authors:  Peggy J Rooney; Lawrence Ayong; Crystal M Tobin; Silvia N J Moreno; Laura J Knoll
Journal:  Mol Biochem Parasitol       Date:  2010-12-30       Impact factor: 1.759

4.  An intracellular phosphate buffer filters transient fluctuations in extracellular phosphate levels.

Authors:  Melissa R Thomas; Erin K O'Shea
Journal:  Proc Natl Acad Sci U S A       Date:  2005-06-22       Impact factor: 11.205

5.  The vacuolar transporter chaperone (VTC) complex is required for microautophagy.

Authors:  Andreas Uttenweiler; Heinz Schwarz; Heinz Neumann; Andreas Mayer
Journal:  Mol Biol Cell       Date:  2006-11-01       Impact factor: 4.138

6.  TOR1 and TOR2 have distinct locations in live cells.

Authors:  Thomas W Sturgill; Adiel Cohen; Melanie Diefenbacher; Mark Trautwein; Dietmar E Martin; Michael N Hall
Journal:  Eukaryot Cell       Date:  2008-08-22

7.  The Vtc proteins in vacuole fusion: coupling NSF activity to V(0) trans-complex formation.

Authors:  Oliver Müller; Martin J Bayer; Christopher Peters; Jens S Andersen; Matthias Mann; Andreas Mayer
Journal:  EMBO J       Date:  2002-02-01       Impact factor: 11.598

8.  Trypanosoma brucei vacuolar transporter chaperone 4 (TbVtc4) is an acidocalcisome polyphosphate kinase required for in vivo infection.

Authors:  Noelia Lander; Paul N Ulrich; Roberto Docampo
Journal:  J Biol Chem       Date:  2013-10-10       Impact factor: 5.157

9.  New components of a system for phosphate accumulation and polyphosphate metabolism in Saccharomyces cerevisiae revealed by genomic expression analysis.

Authors:  N Ogawa; J DeRisi; P O Brown
Journal:  Mol Biol Cell       Date:  2000-12       Impact factor: 4.138

Review 10.  Life in the midst of scarcity: adaptations to nutrient availability in Saccharomyces cerevisiae.

Authors:  Bart Smets; Ruben Ghillebert; Pepijn De Snijder; Matteo Binda; Erwin Swinnen; Claudio De Virgilio; Joris Winderickx
Journal:  Curr Genet       Date:  2010-02       Impact factor: 3.886

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