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Lipid droplet biology and evolution illuminated by the characterization of a novel perilipin in teleost fish
Perilipin (PLIN) proteins constitute an ancient family important in lipid droplet (LD) formation and triglyceride metabolism. We identified an additional PLIN clade (plin6) that is unique to teleosts and can be traced to the two whole genome duplications that occurred early in vertebrate evolution....
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5342826/ https://www.ncbi.nlm.nih.gov/pubmed/28244868 http://dx.doi.org/10.7554/eLife.21771 |
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author | Granneman, James G Kimler, Vickie A Zhang, Huamei Ye, Xiangqun Luo, Xixia Postlethwait, John H Thummel, Ryan |
author_facet | Granneman, James G Kimler, Vickie A Zhang, Huamei Ye, Xiangqun Luo, Xixia Postlethwait, John H Thummel, Ryan |
author_sort | Granneman, James G |
collection | PubMed |
description | Perilipin (PLIN) proteins constitute an ancient family important in lipid droplet (LD) formation and triglyceride metabolism. We identified an additional PLIN clade (plin6) that is unique to teleosts and can be traced to the two whole genome duplications that occurred early in vertebrate evolution. Plin6 is highly expressed in skin xanthophores, which mediate red/yellow pigmentation and trafficking, but not in tissues associated with lipid metabolism. Biochemical and immunochemical analyses demonstrate that zebrafish Plin6 protein targets the surface of pigment-containing carotenoid droplets (CD). Protein kinase A (PKA) activation, which mediates CD dispersion in xanthophores, phosphorylates Plin6 on conserved residues. Knockout of plin6 in zebrafish severely impairs the ability of CD to concentrate carotenoids and prevents tight clustering of CD within carotenoid bodies. Ultrastructural and functional analyses indicate that LD and CD are homologous structures, and that Plin6 was functionalized early in vertebrate evolution for concentrating and trafficking pigment. DOI: http://dx.doi.org/10.7554/eLife.21771.001 |
format | Online Article Text |
id | pubmed-5342826 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-53428262017-03-09 Lipid droplet biology and evolution illuminated by the characterization of a novel perilipin in teleost fish Granneman, James G Kimler, Vickie A Zhang, Huamei Ye, Xiangqun Luo, Xixia Postlethwait, John H Thummel, Ryan eLife Cell Biology Perilipin (PLIN) proteins constitute an ancient family important in lipid droplet (LD) formation and triglyceride metabolism. We identified an additional PLIN clade (plin6) that is unique to teleosts and can be traced to the two whole genome duplications that occurred early in vertebrate evolution. Plin6 is highly expressed in skin xanthophores, which mediate red/yellow pigmentation and trafficking, but not in tissues associated with lipid metabolism. Biochemical and immunochemical analyses demonstrate that zebrafish Plin6 protein targets the surface of pigment-containing carotenoid droplets (CD). Protein kinase A (PKA) activation, which mediates CD dispersion in xanthophores, phosphorylates Plin6 on conserved residues. Knockout of plin6 in zebrafish severely impairs the ability of CD to concentrate carotenoids and prevents tight clustering of CD within carotenoid bodies. Ultrastructural and functional analyses indicate that LD and CD are homologous structures, and that Plin6 was functionalized early in vertebrate evolution for concentrating and trafficking pigment. DOI: http://dx.doi.org/10.7554/eLife.21771.001 eLife Sciences Publications, Ltd 2017-02-28 /pmc/articles/PMC5342826/ /pubmed/28244868 http://dx.doi.org/10.7554/eLife.21771 Text en © 2017, Granneman et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Cell Biology Granneman, James G Kimler, Vickie A Zhang, Huamei Ye, Xiangqun Luo, Xixia Postlethwait, John H Thummel, Ryan Lipid droplet biology and evolution illuminated by the characterization of a novel perilipin in teleost fish |
title | Lipid droplet biology and evolution illuminated by the characterization of a novel perilipin in teleost fish |
title_full | Lipid droplet biology and evolution illuminated by the characterization of a novel perilipin in teleost fish |
title_fullStr | Lipid droplet biology and evolution illuminated by the characterization of a novel perilipin in teleost fish |
title_full_unstemmed | Lipid droplet biology and evolution illuminated by the characterization of a novel perilipin in teleost fish |
title_short | Lipid droplet biology and evolution illuminated by the characterization of a novel perilipin in teleost fish |
title_sort | lipid droplet biology and evolution illuminated by the characterization of a novel perilipin in teleost fish |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5342826/ https://www.ncbi.nlm.nih.gov/pubmed/28244868 http://dx.doi.org/10.7554/eLife.21771 |
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