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dc.contributor.authorMa, Dengke
dc.contributor.authorZheng, Shu
dc.contributor.authorBhatla, Nikhil
dc.contributor.authorPender, Corinne Lenore
dc.contributor.authorRothe, Michael
dc.contributor.authorMenzel, Ralph
dc.contributor.authorHorvitz, Howard Robert
dc.date.accessioned2014-03-28T18:42:23Z
dc.date.available2014-03-28T18:42:23Z
dc.date.issued2013-06
dc.date.submitted2013-01
dc.identifier.issn0036-8075
dc.identifier.issn1095-9203
dc.identifier.urihttp://hdl.handle.net/1721.1/85967
dc.description.abstractOxygen deprivation followed by reoxygenation causes pathological responses in many disorders, including ischemic stroke, heart attacks, and reperfusion injury. Key aspects of ischemia-reperfusion can be modeled by a Caenorhabditis elegans behavior, the O2-ON response, which is suppressed by hypoxic preconditioning or inactivation of the O[subscript 2]-sensing HIF (hypoxia-inducible factor) hydroxylase EGL-9. From a genetic screen, we found that the cytochrome P450 oxygenase CYP-13A12 acts in response to the EGL-9–HIF-1 pathway to facilitate the O2-ON response. CYP-13A12 promotes oxidation of polyunsaturated fatty acids into eicosanoids, signaling molecules that can strongly affect inflammatory pain and ischemia-reperfusion injury responses in mammals. We propose that roles of the EGL-9–HIF-1 pathway and cytochrome P450 in controlling responses to reoxygenation after anoxia are evolutionarily conserved.en_US
dc.description.sponsorshipNational Institutes of Health (U.S.) (Grant GM24663)en_US
dc.description.sponsorshipNational Science Foundation (U.S.). Graduate Research Fellowship Programen_US
dc.description.sponsorshipMassachusetts Institute of Technology. Undergraduate Research Opportunities Programen_US
dc.description.sponsorshipHelen Hay Whitney Foundation (Postdoctoral Fellowship)en_US
dc.language.isoen_US
dc.publisherAmerican Association for the Advancement of Science (AAAS)en_US
dc.relation.isversionofhttp://dx.doi.org/10.1126/science.1235753en_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.sourceHorvitz via Courtney Crummetten_US
dc.titleCytochrome P450 Drives a HIF-Regulated Behavioral Response to Reoxygenation by C. elegansen_US
dc.typeArticleen_US
dc.identifier.citationMa, D. K., M. Rothe, S. Zheng, N. Bhatla, C. L. Pender, R. Menzel, and H. R. Horvitz. “Cytochrome P450 Drives a HIF-Regulated Behavioral Response to Reoxygenation by C. Elegans.” Science 341, no. 6145 (August 2, 2013): 554–558.en_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biologyen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Brain and Cognitive Sciencesen_US
dc.contributor.departmentMcGovern Institute for Brain Research at MITen_US
dc.contributor.departmentKoch Institute for Integrative Cancer Research at MITen_US
dc.contributor.approverHorvitz, H. Roberten_US
dc.contributor.mitauthorMa, Dengkeen_US
dc.contributor.mitauthorZheng, Shuen_US
dc.contributor.mitauthorBhatla, Nikhilen_US
dc.contributor.mitauthorPender, Corinne Lenoreen_US
dc.contributor.mitauthorHorvitz, H. Roberten_US
dc.relation.journalScienceen_US
dc.eprint.versionAuthor's final manuscripten_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsMa, D. K.; Rothe, M.; Zheng, S.; Bhatla, N.; Pender, C. L.; Menzel, R.; Horvitz, H. R.en_US
dc.identifier.orcidhttps://orcid.org/0000-0001-7092-3079
dc.identifier.orcidhttps://orcid.org/0000-0002-9964-9613
dc.identifier.orcidhttps://orcid.org/0000-0002-1693-4524
mit.licensePUBLISHER_POLICYen_US
mit.metadata.statusComplete


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