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http://purl.uniprot.org/citations/36180527http://www.w3.org/1999/02/22-rdf-syntax-ns#typehttp://purl.uniprot.org/core/Journal_Citation
http://purl.uniprot.org/citations/36180527http://www.w3.org/2000/01/rdf-schema#comment"SARS-CoV-2 infection causes COVID-19, a severe acute respiratory disease associated with cardiovascular complications including long-term outcomes. The presence of virus in cardiac tissue of patients with COVID-19 suggests this is a direct, rather than secondary, effect of infection. Here, by expressing individual SARS-CoV-2 proteins in the Drosophila heart, we demonstrate interaction of virus Nsp6 with host proteins of the MGA/MAX complex (MGA, PCGF6 and TFDP1). Complementing transcriptomic data from the fly heart reveal that this interaction blocks the antagonistic MGA/MAX complex, which shifts the balance towards MYC/MAX and activates glycolysis-with similar findings in mouse cardiomyocytes. Further, the Nsp6-induced glycolysis disrupts cardiac mitochondrial function, known to increase reactive oxygen species (ROS) in heart failure; this could explain COVID-19-associated cardiac pathology. Inhibiting the glycolysis pathway by 2-deoxy-D-glucose (2DG) treatment attenuates the Nsp6-induced cardiac phenotype in flies and mice. These findings point to glycolysis as a potential pharmacological target for treating COVID-19-associated heart failure."xsd:string
http://purl.uniprot.org/citations/36180527http://purl.org/dc/terms/identifier"doi:10.1038/s42003-022-03986-6"xsd:string
http://purl.uniprot.org/citations/36180527http://purl.uniprot.org/core/author"Huang X."xsd:string
http://purl.uniprot.org/citations/36180527http://purl.uniprot.org/core/author"Huang W."xsd:string
http://purl.uniprot.org/citations/36180527http://purl.uniprot.org/core/author"Lee H."xsd:string
http://purl.uniprot.org/citations/36180527http://purl.uniprot.org/core/author"Wang G."xsd:string
http://purl.uniprot.org/citations/36180527http://purl.uniprot.org/core/author"Yang P."xsd:string
http://purl.uniprot.org/citations/36180527http://purl.uniprot.org/core/author"Zhu J.Y."xsd:string
http://purl.uniprot.org/citations/36180527http://purl.uniprot.org/core/author"Han Z."xsd:string
http://purl.uniprot.org/citations/36180527http://purl.uniprot.org/core/author"Lee J.G."xsd:string
http://purl.uniprot.org/citations/36180527http://purl.uniprot.org/core/author"Kane M.A."xsd:string
http://purl.uniprot.org/citations/36180527http://purl.uniprot.org/core/author"van de Leemput J."xsd:string
http://purl.uniprot.org/citations/36180527http://purl.uniprot.org/core/author"Yang P.'"xsd:string
http://purl.uniprot.org/citations/36180527http://purl.uniprot.org/core/date"2022"xsd:gYear
http://purl.uniprot.org/citations/36180527http://purl.uniprot.org/core/name"Commun Biol"xsd:string
http://purl.uniprot.org/citations/36180527http://purl.uniprot.org/core/pages"1039"xsd:string
http://purl.uniprot.org/citations/36180527http://purl.uniprot.org/core/title"SARS-CoV-2 Nsp6 damages Drosophila heart and mouse cardiomyocytes through MGA/MAX complex-mediated increased glycolysis."xsd:string
http://purl.uniprot.org/citations/36180527http://purl.uniprot.org/core/volume"5"xsd:string
http://purl.uniprot.org/citations/36180527http://www.w3.org/2004/02/skos/core#exactMatchhttp://purl.uniprot.org/pubmed/36180527
http://purl.uniprot.org/citations/36180527http://xmlns.com/foaf/0.1/primaryTopicOfhttps://pubmed.ncbi.nlm.nih.gov/36180527
http://purl.uniprot.org/uniprot/#_A0A0C4DHC8-mappedCitation-36180527http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/36180527
http://purl.uniprot.org/uniprot/#_A0A0B4KFI7-mappedCitation-36180527http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/36180527
http://purl.uniprot.org/uniprot/#_A0A0B4KEL0-mappedCitation-36180527http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/36180527
http://purl.uniprot.org/uniprot/#_A0A0B4KF99-mappedCitation-36180527http://www.w3.org/1999/02/22-rdf-syntax-ns#objecthttp://purl.uniprot.org/citations/36180527