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Promethin Is a Conserved Seipin Partner Protein
Seipin (BSCL2/SPG17) is a key factor in lipid droplet (LD) biology, and its dysfunction results in severe pathologies, including the fat storage disease Berardinelli-Seip congenital lipodystrophy type 2, as well as several neurological seipinopathies. Despite its importance for human health, the mol...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6468817/ https://www.ncbi.nlm.nih.gov/pubmed/30901948 http://dx.doi.org/10.3390/cells8030268 |
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author | Castro, Inês G. Eisenberg-Bord, Michal Persiani, Elisa Rochford, Justin J. Schuldiner, Maya Bohnert, Maria |
author_facet | Castro, Inês G. Eisenberg-Bord, Michal Persiani, Elisa Rochford, Justin J. Schuldiner, Maya Bohnert, Maria |
author_sort | Castro, Inês G. |
collection | PubMed |
description | Seipin (BSCL2/SPG17) is a key factor in lipid droplet (LD) biology, and its dysfunction results in severe pathologies, including the fat storage disease Berardinelli-Seip congenital lipodystrophy type 2, as well as several neurological seipinopathies. Despite its importance for human health, the molecular role of seipin is still enigmatic. Seipin is evolutionarily conserved from yeast to humans. In yeast, seipin was recently found to cooperate with the lipid droplet organization (LDO) proteins, Ldo16 and Ldo45, two structurally-related proteins involved in LD function and identity that display remote homology to the human protein promethin/TMEM159. In this study, we show that promethin is indeed an LD-associated protein that forms a complex with seipin, and its localization to the LD surface can be modulated by seipin expression levels. We thus identify promethin as a novel seipin partner protein. |
format | Online Article Text |
id | pubmed-6468817 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-64688172019-04-23 Promethin Is a Conserved Seipin Partner Protein Castro, Inês G. Eisenberg-Bord, Michal Persiani, Elisa Rochford, Justin J. Schuldiner, Maya Bohnert, Maria Cells Article Seipin (BSCL2/SPG17) is a key factor in lipid droplet (LD) biology, and its dysfunction results in severe pathologies, including the fat storage disease Berardinelli-Seip congenital lipodystrophy type 2, as well as several neurological seipinopathies. Despite its importance for human health, the molecular role of seipin is still enigmatic. Seipin is evolutionarily conserved from yeast to humans. In yeast, seipin was recently found to cooperate with the lipid droplet organization (LDO) proteins, Ldo16 and Ldo45, two structurally-related proteins involved in LD function and identity that display remote homology to the human protein promethin/TMEM159. In this study, we show that promethin is indeed an LD-associated protein that forms a complex with seipin, and its localization to the LD surface can be modulated by seipin expression levels. We thus identify promethin as a novel seipin partner protein. MDPI 2019-03-21 /pmc/articles/PMC6468817/ /pubmed/30901948 http://dx.doi.org/10.3390/cells8030268 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Castro, Inês G. Eisenberg-Bord, Michal Persiani, Elisa Rochford, Justin J. Schuldiner, Maya Bohnert, Maria Promethin Is a Conserved Seipin Partner Protein |
title | Promethin Is a Conserved Seipin Partner Protein |
title_full | Promethin Is a Conserved Seipin Partner Protein |
title_fullStr | Promethin Is a Conserved Seipin Partner Protein |
title_full_unstemmed | Promethin Is a Conserved Seipin Partner Protein |
title_short | Promethin Is a Conserved Seipin Partner Protein |
title_sort | promethin is a conserved seipin partner protein |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6468817/ https://www.ncbi.nlm.nih.gov/pubmed/30901948 http://dx.doi.org/10.3390/cells8030268 |
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