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Peroxisomal Membrane Proteins Insert into the Endoplasmic Reticulum

We show that a comprehensive set of 16 peroxisomal membrane proteins (PMPs) encompassing all types of membrane topologies first target to the endoplasmic reticulum (ER) in Saccharomyces cerevisiae. These PMPs insert into the ER membrane via the protein import complexes Sec61p and Get3p (for tail-anc...

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Detalles Bibliográficos
Autores principales: van der Zand, Adabella, Braakman, Ineke, Tabak, Henk F.
Formato: Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883949/
https://www.ncbi.nlm.nih.gov/pubmed/20427571
http://dx.doi.org/10.1091/mbc.E10-02-0082
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author van der Zand, Adabella
Braakman, Ineke
Tabak, Henk F.
author_facet van der Zand, Adabella
Braakman, Ineke
Tabak, Henk F.
author_sort van der Zand, Adabella
collection PubMed
description We show that a comprehensive set of 16 peroxisomal membrane proteins (PMPs) encompassing all types of membrane topologies first target to the endoplasmic reticulum (ER) in Saccharomyces cerevisiae. These PMPs insert into the ER membrane via the protein import complexes Sec61p and Get3p (for tail-anchored proteins). This trafficking pathway is representative for multiplying wild-type cells in which the peroxisome population needs to be maintained, as well as for mutant cells lacking peroxisomes in which new peroxisomes form after complementation with the wild-type version of the mutant gene. PMPs leave the ER in a Pex3p-Pex19p–dependent manner to end up in metabolically active peroxisomes. These results further extend the new concept that peroxisomes derive their basic framework (membrane and membrane proteins) from the ER and imply a new functional role for Pex3p and Pex19p.
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spelling pubmed-28839492010-08-30 Peroxisomal Membrane Proteins Insert into the Endoplasmic Reticulum van der Zand, Adabella Braakman, Ineke Tabak, Henk F. Mol Biol Cell Articles We show that a comprehensive set of 16 peroxisomal membrane proteins (PMPs) encompassing all types of membrane topologies first target to the endoplasmic reticulum (ER) in Saccharomyces cerevisiae. These PMPs insert into the ER membrane via the protein import complexes Sec61p and Get3p (for tail-anchored proteins). This trafficking pathway is representative for multiplying wild-type cells in which the peroxisome population needs to be maintained, as well as for mutant cells lacking peroxisomes in which new peroxisomes form after complementation with the wild-type version of the mutant gene. PMPs leave the ER in a Pex3p-Pex19p–dependent manner to end up in metabolically active peroxisomes. These results further extend the new concept that peroxisomes derive their basic framework (membrane and membrane proteins) from the ER and imply a new functional role for Pex3p and Pex19p. The American Society for Cell Biology 2010-06-15 /pmc/articles/PMC2883949/ /pubmed/20427571 http://dx.doi.org/10.1091/mbc.E10-02-0082 Text en © 2010 by The American Society for Cell Biology
spellingShingle Articles
van der Zand, Adabella
Braakman, Ineke
Tabak, Henk F.
Peroxisomal Membrane Proteins Insert into the Endoplasmic Reticulum
title Peroxisomal Membrane Proteins Insert into the Endoplasmic Reticulum
title_full Peroxisomal Membrane Proteins Insert into the Endoplasmic Reticulum
title_fullStr Peroxisomal Membrane Proteins Insert into the Endoplasmic Reticulum
title_full_unstemmed Peroxisomal Membrane Proteins Insert into the Endoplasmic Reticulum
title_short Peroxisomal Membrane Proteins Insert into the Endoplasmic Reticulum
title_sort peroxisomal membrane proteins insert into the endoplasmic reticulum
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2883949/
https://www.ncbi.nlm.nih.gov/pubmed/20427571
http://dx.doi.org/10.1091/mbc.E10-02-0082
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