<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Mohl BP</submitter><funding>Wellcome Trust</funding><pagination>680-693</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC5115167</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>97(3)</volume><pubmed_abstract>Hepatitis C virus (HCV) infection has been shown to induce autophagy but the mechanisms underpinning this process remain to be elucidated. Induction of autophagy requires the class III phosphatidylinositol 3-kinase, Vps34, which produces phosphatidylinositol 3-phosphate (PI3P) within the endoplasmic reticulum (ER) membrane. This recruits proteins with PI3P binding domains such as the double-FYVE-containing protein 1 (DFCP1). DFCP1 generates cup-shaped protrusions from the ER membrane, termed omegasomes, which provide a platform for the production of autophagosomes. Here we present data demonstrating that both Vps34 and DFCP1 are required for HCV genome replication, in the context of both a subgenomic replicon and virus infection, but did not affect virus entry or initial translation. Using</pubmed_abstract><journal>The Journal of general virology</journal><pubmed_title>Early events in the generation of autophagosomes are required for the formation of membrane structures involved in hepatitis C virus genome replication.</pubmed_title><pmcid>PMC5115167</pmcid><funding_grant_id>096670</funding_grant_id><funding_grant_id>099759</funding_grant_id><pubmed_authors>Harris M</pubmed_authors><pubmed_authors>Mankouri J</pubmed_authors><pubmed_authors>Bartlett C</pubmed_authors><pubmed_authors>Mohl BP</pubmed_authors></additional><is_claimable>false</is_claimable><name>Early events in the generation of autophagosomes are required for the formation of membrane structures involved in hepatitis C virus genome replication.</name><description>Hepatitis C virus (HCV) infection has been shown to induce autophagy but the mechanisms underpinning this process remain to be elucidated. Induction of autophagy requires the class III phosphatidylinositol 3-kinase, Vps34, which produces phosphatidylinositol 3-phosphate (PI3P) within the endoplasmic reticulum (ER) membrane. This recruits proteins with PI3P binding domains such as the double-FYVE-containing protein 1 (DFCP1). DFCP1 generates cup-shaped protrusions from the ER membrane, termed omegasomes, which provide a platform for the production of autophagosomes. Here we present data demonstrating that both Vps34 and DFCP1 are required for HCV genome replication, in the context of both a subgenomic replicon and virus infection, but did not affect virus entry or initial translation. Using</description><dates><release>2016-01-01T00:00:00Z</release><publication>2016 Mar</publication><modification>2025-04-19T03:03:33.707Z</modification><creation>2019-03-26T23:38:21Z</creation></dates><accession>S-EPMC5115167</accession><cross_references><pubmed>26727924</pubmed><doi>10.1099/jgv.0.000387</doi></cross_references></HashMap>