<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zirin J</submitter><funding>NIDDK NIH HHS</funding><funding>Howard Hughes Medical Institute</funding><funding>NCI NIH HHS</funding><funding>NIAMS NIH HHS</funding><funding>NIGMS NIH HHS</funding><pagination>e1005006</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4334200</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(2)</volume><pubmed_abstract>Given the diversity of autophagy targets and regulation, it is important to characterize autophagy in various cell types and conditions. We used a primary myocyte cell culture system to assay the role of putative autophagy regulators in the specific context of skeletal muscle. By treating the cultures with rapamycin (Rap) and chloroquine (CQ) we induced an autophagic response, fully suppressible by knockdown of core ATG genes. We screened D. melanogaster orthologs of a previously reported mammalian autophagy protein-protein interaction network, identifying several proteins required for autophagosome formation in muscle cells, including orthologs of the Rab regulators RabGap1 and Rab3Gap1. The screen also highlighted the critical roles of the proteasome and glycogen metabolism in regulating</pubmed_abstract><journal>PLoS genetics</journal><pubmed_title>Regulators of autophagosome formation in Drosophila muscles.</pubmed_title><pmcid>PMC4334200</pmcid><funding_grant_id>F32GM082174-02</funding_grant_id><funding_grant_id>R01 AR057352</funding_grant_id><funding_grant_id>R01 DK088718</funding_grant_id><funding_grant_id>F32 GM082174</funding_grant_id><funding_grant_id>AR057352</funding_grant_id><funding_grant_id>P01CA120964</funding_grant_id><funding_grant_id>P01 CA120964</funding_grant_id><pubmed_authors>Perrimon N</pubmed_authors><pubmed_authors>Zirin J</pubmed_authors><pubmed_authors>Nieuwenhuis J</pubmed_authors><pubmed_authors>Samsonova A</pubmed_authors><pubmed_authors>Tao R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Regulators of autophagosome formation in Drosophila muscles.</name><description>Given the diversity of autophagy targets and regulation, it is important to characterize autophagy in various cell types and conditions. We used a primary myocyte cell culture system to assay the role of putative autophagy regulators in the specific context of skeletal muscle. By treating the cultures with rapamycin (Rap) and chloroquine (CQ) we induced an autophagic response, fully suppressible by knockdown of core ATG genes. We screened D. melanogaster orthologs of a previously reported mammalian autophagy protein-protein interaction network, identifying several proteins required for autophagosome formation in muscle cells, including orthologs of the Rab regulators RabGap1 and Rab3Gap1. The screen also highlighted the critical roles of the proteasome and glycogen metabolism in regulating</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Feb</publication><modification>2025-05-29T21:21:45.408Z</modification><creation>2025-05-29T21:21:45.408Z</creation></dates><accession>S-EPMC4334200</accession><cross_references><pubmed>25692684</pubmed><doi>10.1371/journal.pgen.1005006</doi></cross_references></HashMap>