Please use this identifier to cite or link to this item: https://doi.org/10.1038/ncomms13150
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dc.titleHuman genome-wide RNAi screen reveals host factors required for enterovirus 71 replication
dc.contributor.authorWu, Kan Xing
dc.contributor.authorPATCHARA PHUEKTES
dc.contributor.authorKumar, Pankaj
dc.contributor.authorGoh, Germaine Yen Lin
dc.contributor.authorMoreau, Dimitri
dc.contributor.authorCHOW TAK KWONG,VINCENT
dc.contributor.authorFREDERIC BARD
dc.contributor.authorCHU JANG HANN
dc.date.accessioned2020-06-24T03:50:40Z
dc.date.available2020-06-24T03:50:40Z
dc.date.issued2016-10-17
dc.identifier.citationWu, Kan Xing, PATCHARA PHUEKTES, Kumar, Pankaj, Goh, Germaine Yen Lin, Moreau, Dimitri, CHOW TAK KWONG,VINCENT, FREDERIC BARD, CHU JANG HANN (2016-10-17). Human genome-wide RNAi screen reveals host factors required for enterovirus 71 replication. NATURE COMMUNICATIONS 7 (1). ScholarBank@NUS Repository. https://doi.org/10.1038/ncomms13150
dc.identifier.issn2041-1723
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/170677
dc.description.abstract© 2016 The Author(s). Enterovirus 71 (EV71) is a neurotropic enterovirus without antivirals or vaccine, and its host-pathogen interactions remain poorly understood. Here we use a human genome-wide RNAi screen to identify 256 host factors involved in EV71 replication in human rhabdomyosarcoma cells. Enrichment analyses reveal overrepresentation in processes like mitotic cell cycle and transcriptional regulation. We have carried out orthogonal experiments to characterize the roles of selected factors involved in cell cycle regulation and endoplasmatic reticulum-associated degradation. We demonstrate nuclear egress of CDK6 in EV71 infected cells, and identify CDK6 and AURKB as resistance factors. NGLY1, which co-localizes with EV71 replication complexes at the endoplasmatic reticulum, supports EV71 replication. We confirm importance of these factors for EV71 replication in a human neuronal cell line and for coxsackievirus A16 infection. A small molecule inhibitor of NGLY1 reduces EV71 replication. This study provides a comprehensive map of EV71 host factors and reveals potential antiviral targets.
dc.language.isoen
dc.publisherNATURE PUBLISHING GROUP
dc.sourceElements
dc.subjectScience & Technology
dc.subjectMultidisciplinary Sciences
dc.subjectScience & Technology - Other Topics
dc.subjectRIBOSOMAL ENTRY SITE
dc.subjectPEPTIDE-N-GLYCANASE
dc.subjectERM PROTEINS
dc.subjectAURORA-B
dc.subjectINFECTION
dc.subjectBINDS
dc.subjectINHIBITOR
dc.subjectAUTOPHAGY
dc.subjectRECEPTOR
dc.subjectRADIXIN
dc.typeArticle
dc.date.updated2020-06-23T08:03:03Z
dc.contributor.departmentBIOCHEMISTRY
dc.contributor.departmentMICROBIOLOGY AND IMMUNOLOGY
dc.description.doi10.1038/ncomms13150
dc.description.sourcetitleNATURE COMMUNICATIONS
dc.description.volume7
dc.description.issue1
dc.published.statePublished
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