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dc.contributor.authorLi, Yun
dc.contributor.authorMuffat, Julien
dc.contributor.authorOmer Javed, Attya
dc.contributor.authorKeys, Heather R.
dc.contributor.authorLungjangwa, Tenzin
dc.contributor.authorBosch, Irene
dc.contributor.authorKhan, Mehreen
dc.contributor.authorVirgilio, Maria C.
dc.contributor.authorGehrke, Lee
dc.contributor.authorSabatini, David M.
dc.contributor.authorJaenisch, Rudolf
dc.date.accessioned2020-05-07T13:32:10Z
dc.date.available2020-05-07T13:32:10Z
dc.date.issued2019-04
dc.date.submitted2019-03
dc.identifier.issn0027-8424
dc.identifier.issn1091-6490
dc.identifier.urihttps://hdl.handle.net/1721.1/125089
dc.description.abstractZika virus (ZIKV) is a neurotropic and neurovirulent arbovirus that has severe detrimental impact on the developing human fetal brain. To date, little is known about the factors required for ZIKV infection of human neural cells. We identified ZIKV host genes in human pluripotent stem cell (hPSC)-derived neural progenitors (NPs) using a genome-wide CRISPR-Cas9 knockout screen. Mutations of host factors involved in heparan sulfation, endocytosis, endoplasmic reticulum processing, Golgi function, and interferon activity conferred resistance to infection with the Uganda strain of ZIKV and a more recent North American isolate. Host genes essential for ZIKV replication identified in human NPs also provided a low level of protection against ZIKV in isogenic human astrocytes. Our findings provide insights into host-dependent mechanisms for ZIKV infection in the highly vulnerable human NP cells and identify molecular targets for potential therapeutic intervention. Keywords: Zika virus; neural progenitors; CRISPR screen; fetal CNS infection; human pluri; potent stem cellsen_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant R01 MH104610)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant R01 NS088538)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant U19 AI131135)en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant R33 AI100190)en_US
dc.description.sponsorshipSimons Foundation (Grant SFARI 204106)en_US
dc.language.isoen
dc.publisherNational Academy of Sciencesen_US
dc.relation.isversionofhttp://dx.doi.org/10.1073/pnas.1900867116en_US
dc.rightsArticle is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use.en_US
dc.sourcePNASen_US
dc.subjectMultidisciplinaryen_US
dc.titleGenome-wide CRISPR screen for Zika virus resistance in human neural cellsen_US
dc.typeArticleen_US
dc.identifier.citationLi, Yun et al. "Genome-wide CRISPR screen for Zika virus resistance in human neural cells." Proceedings of the National Academy of Sciences of the United States of Americas 116, 19 (May 2019): 9527-9532 ©2019 National Academy of Sciences.en_US
dc.contributor.departmentWhitehead Institute for Biomedical Researchen_US
dc.contributor.departmentMassachusetts Institute of Technology. Institute for Medical Engineering & Scienceen_US
dc.contributor.departmentBroad Institute of MIT and Harvarden_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.relation.journalProceedings of the National Academy of Sciences of the United States of Americaen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2019-10-09T13:55:27Z
dspace.date.submission2019-10-09T13:55:29Z
mit.journal.volume116en_US
mit.journal.issue19en_US
mit.metadata.statusComplete


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