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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2017
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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. |
format | Online Article Text |
id | pubmed-5499832 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
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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