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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...

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Autores principales: Castro, Inês G., Eisenberg-Bord, Michal, Persiani, Elisa, Rochford, Justin J., Schuldiner, Maya, Bohnert, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
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.
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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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