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The Phospholipid:Diacylglycerol Acyltransferase Lro1 Is Responsible for Hepatitis C Virus Core-Induced Lipid Droplet Formation in a Yeast Model System

Chronic infection with the hepatitis C virus frequently induces steatosis, which is a significant risk factor for liver pathogenesis. Steatosis is characterized by the accumulation of lipid droplets in hepatocytes. The structural protein core of the virus induces lipid droplet formation and localize...

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Autores principales: Iwasa, Shingo, Sato, Naoko, Wang, Chao-Wen, Cheng, Yun-Hsin, Irokawa, Hayato, Hwang, Gi-Wook, Naganuma, Akira, Kuge, Shusuke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4961368/
https://www.ncbi.nlm.nih.gov/pubmed/27459103
http://dx.doi.org/10.1371/journal.pone.0159324
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author Iwasa, Shingo
Sato, Naoko
Wang, Chao-Wen
Cheng, Yun-Hsin
Irokawa, Hayato
Hwang, Gi-Wook
Naganuma, Akira
Kuge, Shusuke
author_facet Iwasa, Shingo
Sato, Naoko
Wang, Chao-Wen
Cheng, Yun-Hsin
Irokawa, Hayato
Hwang, Gi-Wook
Naganuma, Akira
Kuge, Shusuke
author_sort Iwasa, Shingo
collection PubMed
description Chronic infection with the hepatitis C virus frequently induces steatosis, which is a significant risk factor for liver pathogenesis. Steatosis is characterized by the accumulation of lipid droplets in hepatocytes. The structural protein core of the virus induces lipid droplet formation and localizes on the surface of the lipid droplets. However, the precise molecular mechanisms for the core-induced formation of lipid droplets remain elusive. Recently, we showed that the expression of the core protein in yeast as a model system could induce lipid droplet formation. In this study, we probed the cellular factors responsible for the formation of core-induced lipid-droplets in yeast cells. We demonstrated that one of the enzymes responsible for triglyceride synthesis, a phospholipid:diacylglycerol acyltransferase (Lro1), is required for the core-induced lipid droplet formation. While core proteins inhibit Lro1 degradation and alter Lro1 localization, the characteristic localization of Lro1 adjacent to the lipid droplets appeared to be responsible for the core-induced lipid droplet formation. RNA virus genomes have evolved using high mutation rates to maintain their ability to replicate. Our observations suggest a functional relationship between the core protein with hepatocytes and yeast cells. The possible interactions between core proteins and the endoplasmic reticulum membrane affect the mobilization of specific proteins.
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spelling pubmed-49613682016-08-08 The Phospholipid:Diacylglycerol Acyltransferase Lro1 Is Responsible for Hepatitis C Virus Core-Induced Lipid Droplet Formation in a Yeast Model System Iwasa, Shingo Sato, Naoko Wang, Chao-Wen Cheng, Yun-Hsin Irokawa, Hayato Hwang, Gi-Wook Naganuma, Akira Kuge, Shusuke PLoS One Research Article Chronic infection with the hepatitis C virus frequently induces steatosis, which is a significant risk factor for liver pathogenesis. Steatosis is characterized by the accumulation of lipid droplets in hepatocytes. The structural protein core of the virus induces lipid droplet formation and localizes on the surface of the lipid droplets. However, the precise molecular mechanisms for the core-induced formation of lipid droplets remain elusive. Recently, we showed that the expression of the core protein in yeast as a model system could induce lipid droplet formation. In this study, we probed the cellular factors responsible for the formation of core-induced lipid-droplets in yeast cells. We demonstrated that one of the enzymes responsible for triglyceride synthesis, a phospholipid:diacylglycerol acyltransferase (Lro1), is required for the core-induced lipid droplet formation. While core proteins inhibit Lro1 degradation and alter Lro1 localization, the characteristic localization of Lro1 adjacent to the lipid droplets appeared to be responsible for the core-induced lipid droplet formation. RNA virus genomes have evolved using high mutation rates to maintain their ability to replicate. Our observations suggest a functional relationship between the core protein with hepatocytes and yeast cells. The possible interactions between core proteins and the endoplasmic reticulum membrane affect the mobilization of specific proteins. Public Library of Science 2016-07-26 /pmc/articles/PMC4961368/ /pubmed/27459103 http://dx.doi.org/10.1371/journal.pone.0159324 Text en © 2016 Iwasa et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Iwasa, Shingo
Sato, Naoko
Wang, Chao-Wen
Cheng, Yun-Hsin
Irokawa, Hayato
Hwang, Gi-Wook
Naganuma, Akira
Kuge, Shusuke
The Phospholipid:Diacylglycerol Acyltransferase Lro1 Is Responsible for Hepatitis C Virus Core-Induced Lipid Droplet Formation in a Yeast Model System
title The Phospholipid:Diacylglycerol Acyltransferase Lro1 Is Responsible for Hepatitis C Virus Core-Induced Lipid Droplet Formation in a Yeast Model System
title_full The Phospholipid:Diacylglycerol Acyltransferase Lro1 Is Responsible for Hepatitis C Virus Core-Induced Lipid Droplet Formation in a Yeast Model System
title_fullStr The Phospholipid:Diacylglycerol Acyltransferase Lro1 Is Responsible for Hepatitis C Virus Core-Induced Lipid Droplet Formation in a Yeast Model System
title_full_unstemmed The Phospholipid:Diacylglycerol Acyltransferase Lro1 Is Responsible for Hepatitis C Virus Core-Induced Lipid Droplet Formation in a Yeast Model System
title_short The Phospholipid:Diacylglycerol Acyltransferase Lro1 Is Responsible for Hepatitis C Virus Core-Induced Lipid Droplet Formation in a Yeast Model System
title_sort phospholipid:diacylglycerol acyltransferase lro1 is responsible for hepatitis c virus core-induced lipid droplet formation in a yeast model system
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4961368/
https://www.ncbi.nlm.nih.gov/pubmed/27459103
http://dx.doi.org/10.1371/journal.pone.0159324
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