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Peroxisomal ACBD4 interacts with VAPB and promotes ER-peroxisome associations

Cooperation between cellular organelles such as mitochondria, peroxisomes and the ER is essential for a variety of important and diverse metabolic processes. Effective communication and metabolite exchange requires physical linkages between the organelles, predominantly in the form of organelle cont...

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Autores principales: Costello, Joseph L., Castro, Inês G., Schrader, Tina A., Islinger, Markus, Schrader, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5499832/
https://www.ncbi.nlm.nih.gov/pubmed/28463579
http://dx.doi.org/10.1080/15384101.2017.1314422
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author Costello, Joseph L.
Castro, Inês G.
Schrader, Tina A.
Islinger, Markus
Schrader, Michael
author_facet Costello, Joseph L.
Castro, Inês G.
Schrader, Tina A.
Islinger, Markus
Schrader, Michael
author_sort Costello, Joseph L.
collection PubMed
description Cooperation between cellular organelles such as mitochondria, peroxisomes and the ER is essential for a variety of important and diverse metabolic processes. Effective communication and metabolite exchange requires physical linkages between the organelles, predominantly in the form of organelle contact sites. At such contact sites organelle membranes are brought into close proximity by the action of molecular tethers, which often consist of specific protein pairs anchored in the membrane of the opposing organelles. Currently numerous tethering components have been identified which link the ER with multiple other organelles but knowledge of the factors linking the ER with peroxisomes is limited. Peroxisome-ER interplay is important because it is required for the biosynthesis of unsaturated fatty acids, ether-phospholipids and sterols with defects in these functions leading to severe diseases. Here, we characterize acyl-CoA binding domain protein 4 (ACBD4) as a tail-anchored peroxisomal membrane protein which interacts with the ER protein, vesicle-associated membrane protein-associated protein–B (VAPB) to promote peroxisome-ER associations.
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spelling pubmed-54998322017-07-11 Peroxisomal ACBD4 interacts with VAPB and promotes ER-peroxisome associations Costello, Joseph L. Castro, Inês G. Schrader, Tina A. Islinger, Markus Schrader, Michael Cell Cycle Extra View Cooperation between cellular organelles such as mitochondria, peroxisomes and the ER is essential for a variety of important and diverse metabolic processes. Effective communication and metabolite exchange requires physical linkages between the organelles, predominantly in the form of organelle contact sites. At such contact sites organelle membranes are brought into close proximity by the action of molecular tethers, which often consist of specific protein pairs anchored in the membrane of the opposing organelles. Currently numerous tethering components have been identified which link the ER with multiple other organelles but knowledge of the factors linking the ER with peroxisomes is limited. Peroxisome-ER interplay is important because it is required for the biosynthesis of unsaturated fatty acids, ether-phospholipids and sterols with defects in these functions leading to severe diseases. Here, we characterize acyl-CoA binding domain protein 4 (ACBD4) as a tail-anchored peroxisomal membrane protein which interacts with the ER protein, vesicle-associated membrane protein-associated protein–B (VAPB) to promote peroxisome-ER associations. Taylor & Francis 2017-05-02 /pmc/articles/PMC5499832/ /pubmed/28463579 http://dx.doi.org/10.1080/15384101.2017.1314422 Text en © 2017 The Author(s). Published with license by Taylor & Francis http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted.
spellingShingle Extra View
Costello, Joseph L.
Castro, Inês G.
Schrader, Tina A.
Islinger, Markus
Schrader, Michael
Peroxisomal ACBD4 interacts with VAPB and promotes ER-peroxisome associations
title Peroxisomal ACBD4 interacts with VAPB and promotes ER-peroxisome associations
title_full Peroxisomal ACBD4 interacts with VAPB and promotes ER-peroxisome associations
title_fullStr Peroxisomal ACBD4 interacts with VAPB and promotes ER-peroxisome associations
title_full_unstemmed Peroxisomal ACBD4 interacts with VAPB and promotes ER-peroxisome associations
title_short Peroxisomal ACBD4 interacts with VAPB and promotes ER-peroxisome associations
title_sort peroxisomal acbd4 interacts with vapb and promotes er-peroxisome associations
topic Extra View
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5499832/
https://www.ncbi.nlm.nih.gov/pubmed/28463579
http://dx.doi.org/10.1080/15384101.2017.1314422
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