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PEX11 promotes peroxisome division independently of peroxisome metabolism

The PEX11 peroxisomal membrane proteins are the only factors known to promote peroxisome division in multiple species. It has been proposed that PEX11 proteins have a direct role in peroxisomal fatty acid oxidation, and that they only affect peroxisome abundance indirectly. Here we show that PEX11 p...

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Detalles Bibliográficos
Autores principales: Li, Xiaoling, Gould, Stephen J.
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2174077/
https://www.ncbi.nlm.nih.gov/pubmed/11839773
http://dx.doi.org/10.1083/jcb.200112028
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author Li, Xiaoling
Gould, Stephen J.
author_facet Li, Xiaoling
Gould, Stephen J.
author_sort Li, Xiaoling
collection PubMed
description The PEX11 peroxisomal membrane proteins are the only factors known to promote peroxisome division in multiple species. It has been proposed that PEX11 proteins have a direct role in peroxisomal fatty acid oxidation, and that they only affect peroxisome abundance indirectly. Here we show that PEX11 proteins are unique in their ability to promote peroxisome division, and that PEX11 overexpression promotes peroxisome division in the absence of peroxisomal metabolic activity. We also observed that mouse cells lacking PEX11β display reduced peroxisome abundance, even in the absence of peroxisomal metabolic substrates, and that PEX11β(−) (/) (−) mice are partially deficient in two distinct peroxisomal metabolic pathways, ether lipid synthesis and very long chain fatty acid oxidation. Based on these and other observations, we propose that PEX11 proteins act directly in peroxisome division, and that their loss has indirect effects on peroxisome metabolism.
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spelling pubmed-21740772008-05-01 PEX11 promotes peroxisome division independently of peroxisome metabolism Li, Xiaoling Gould, Stephen J. J Cell Biol Article The PEX11 peroxisomal membrane proteins are the only factors known to promote peroxisome division in multiple species. It has been proposed that PEX11 proteins have a direct role in peroxisomal fatty acid oxidation, and that they only affect peroxisome abundance indirectly. Here we show that PEX11 proteins are unique in their ability to promote peroxisome division, and that PEX11 overexpression promotes peroxisome division in the absence of peroxisomal metabolic activity. We also observed that mouse cells lacking PEX11β display reduced peroxisome abundance, even in the absence of peroxisomal metabolic substrates, and that PEX11β(−) (/) (−) mice are partially deficient in two distinct peroxisomal metabolic pathways, ether lipid synthesis and very long chain fatty acid oxidation. Based on these and other observations, we propose that PEX11 proteins act directly in peroxisome division, and that their loss has indirect effects on peroxisome metabolism. The Rockefeller University Press 2002-02-18 /pmc/articles/PMC2174077/ /pubmed/11839773 http://dx.doi.org/10.1083/jcb.200112028 Text en Copyright © 2002, The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/).
spellingShingle Article
Li, Xiaoling
Gould, Stephen J.
PEX11 promotes peroxisome division independently of peroxisome metabolism
title PEX11 promotes peroxisome division independently of peroxisome metabolism
title_full PEX11 promotes peroxisome division independently of peroxisome metabolism
title_fullStr PEX11 promotes peroxisome division independently of peroxisome metabolism
title_full_unstemmed PEX11 promotes peroxisome division independently of peroxisome metabolism
title_short PEX11 promotes peroxisome division independently of peroxisome metabolism
title_sort pex11 promotes peroxisome division independently of peroxisome metabolism
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2174077/
https://www.ncbi.nlm.nih.gov/pubmed/11839773
http://dx.doi.org/10.1083/jcb.200112028
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