Literature DB >> 9435273

The role of yeast VDAC genes on the permeability of the mitochondrial outer membrane.

A C Lee1, X Xu, E Blachly-Dyson, M Forte, M Colombini.   

Abstract

In addition to the POR1 gene, which encodes the well-characterized voltage dependent anion-selective channel (YVDAC1) of the mitochondrial outer membrane, the yeast Saccharomyces cerevisiae contains a second gene (POR2) encoding a protein (YVDAC2) with 50% sequence identity to YVDAC1. Mitochondria isolated from yeast cells deleted for the POR1 gene (delta por1) had a profoundly reduced outer membrane permeability as measured by the ability of an intermembrane space dehydrogenase to oxidize exogenously added NADH. Mitochondria missing either YVDAC1 or both YVDAC1 and YVDAC2 showed a 2-fold increase in the rate of NADH oxidation when the outer membrane was deliberately damaged. Mitochondria from parental cells showed only a 10% increase indicating that the outer membrane is highly permeable to NADH. In the absence of YVDAC1, we calculate that the outer membrane permeability to NADH is reduced 20-fold. The low NADH permeability in the presence of YVDAC2 was not due to the low levels of YVDAC2 expression as mitochondria from cells expressing levels of YVDAC2 comparable to those of YVDAC1 in parental cells showed no substantial increase in NADH permeability, indicating a minimal role of YVDAC2 in this permeability. The residual permeability may be due to other pathways because cells missing both genes can still grow on nonfermentable carbon sources. However, YVDAC1 is clearly the major pathway for NADH flux through the outer membrane in these mitochondria.

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Year:  1998        PMID: 9435273     DOI: 10.1007/s002329900324

Source DB:  PubMed          Journal:  J Membr Biol        ISSN: 0022-2631            Impact factor:   1.843


  56 in total

1.  NADH is specifically channeled through the mitochondrial porin channel in Saccharomyces cerevisiae.

Authors:  N Avéret; H Aguilaniu; O Bunoust; L Gustafsson; M Rigoulet
Journal:  J Bioenerg Biomembr       Date:  2002-12       Impact factor: 2.945

2.  Bax oligomerization in mitochondrial membranes requires tBid (caspase-8-cleaved Bid) and a mitochondrial protein.

Authors:  Xavier Roucou; Sylvie Montessuit; Bruno Antonsson; Jean-Claude Martinou
Journal:  Biochem J       Date:  2002-12-15       Impact factor: 3.857

3.  Response of yeast to the regulated expression of proteins in the Bcl-2 family.

Authors:  Peter Polcic; Michael Forte
Journal:  Biochem J       Date:  2003-09-01       Impact factor: 3.857

4.  VDAC: the channel at the interface between mitochondria and the cytosol.

Authors:  Marco Colombini
Journal:  Mol Cell Biochem       Date:  2004 Jan-Feb       Impact factor: 3.396

5.  VDAC contributes to mRNA levels in Saccharomyces cerevisiae cells by the intracellular reduction/oxidation state dependent and independent mechanisms.

Authors:  Hanna Gałgańska; Monika Antoniewicz; Małgorzata Budzińska; Lukasz Gałgański; Hanna Kmita
Journal:  J Bioenerg Biomembr       Date:  2010-11-12       Impact factor: 2.945

6.  Quantitative- and phospho-proteomic analysis of the yeast response to the tyrosine kinase inhibitor imatinib to pharmacoproteomics-guided drug line extension.

Authors:  Sandra C Dos Santos; Nuno P Mira; Ana S Moreira; Isabel Sá-Correia
Journal:  OMICS       Date:  2012-07-09

7.  New insights into the mechanism of permeation through large channels.

Authors:  Alexander G Komarov; Defeng Deng; William J Craigen; Marco Colombini
Journal:  Biophys J       Date:  2005-09-30       Impact factor: 4.033

Review 8.  Specific VDAC inhibitors: phosphorothioate oligonucleotides.

Authors:  C A Stein; Marco Colombini
Journal:  J Bioenerg Biomembr       Date:  2008-06       Impact factor: 2.945

Review 9.  Voltage-dependent anion channels: their roles in plant defense and cell death.

Authors:  Tomonobu Kusano; Chika Tateda; Thomas Berberich; Yoshihiro Takahashi
Journal:  Plant Cell Rep       Date:  2009-07-08       Impact factor: 4.570

10.  Molecular and cell biology of a family of voltage-dependent anion channel porins in Lotus japonicus.

Authors:  Maren Wandrey; Ben Trevaskis; Nick Brewin; Michael K Udvardi
Journal:  Plant Physiol       Date:  2003-12-04       Impact factor: 8.340

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