dc.contributor.author | Ma, Dengke | |
dc.contributor.author | Zheng, Shu | |
dc.contributor.author | Bhatla, Nikhil | |
dc.contributor.author | Pender, Corinne Lenore | |
dc.contributor.author | Rothe, Michael | |
dc.contributor.author | Menzel, Ralph | |
dc.contributor.author | Horvitz, Howard Robert | |
dc.date.accessioned | 2014-03-28T18:42:23Z | |
dc.date.available | 2014-03-28T18:42:23Z | |
dc.date.issued | 2013-06 | |
dc.date.submitted | 2013-01 | |
dc.identifier.issn | 0036-8075 | |
dc.identifier.issn | 1095-9203 | |
dc.identifier.uri | http://hdl.handle.net/1721.1/85967 | |
dc.description.abstract | Oxygen 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.sponsorship | National Institutes of Health (U.S.) (Grant GM24663) | en_US |
dc.description.sponsorship | National Science Foundation (U.S.). Graduate Research Fellowship Program | en_US |
dc.description.sponsorship | Massachusetts Institute of Technology. Undergraduate Research Opportunities Program | en_US |
dc.description.sponsorship | Helen Hay Whitney Foundation (Postdoctoral Fellowship) | en_US |
dc.language.iso | en_US | |
dc.publisher | American Association for the Advancement of Science (AAAS) | en_US |
dc.relation.isversionof | http://dx.doi.org/10.1126/science.1235753 | en_US |
dc.rights | Article 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.source | Horvitz via Courtney Crummett | en_US |
dc.title | Cytochrome P450 Drives a HIF-Regulated Behavioral Response to Reoxygenation by C. elegans | en_US |
dc.type | Article | en_US |
dc.identifier.citation | Ma, 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.department | Massachusetts Institute of Technology. Department of Biology | en_US |
dc.contributor.department | Massachusetts Institute of Technology. Department of Brain and Cognitive Sciences | en_US |
dc.contributor.department | McGovern Institute for Brain Research at MIT | en_US |
dc.contributor.department | Koch Institute for Integrative Cancer Research at MIT | en_US |
dc.contributor.approver | Horvitz, H. Robert | en_US |
dc.contributor.mitauthor | Ma, Dengke | en_US |
dc.contributor.mitauthor | Zheng, Shu | en_US |
dc.contributor.mitauthor | Bhatla, Nikhil | en_US |
dc.contributor.mitauthor | Pender, Corinne Lenore | en_US |
dc.contributor.mitauthor | Horvitz, H. Robert | en_US |
dc.relation.journal | Science | en_US |
dc.eprint.version | Author's final manuscript | en_US |
dc.type.uri | http://purl.org/eprint/type/JournalArticle | en_US |
eprint.status | http://purl.org/eprint/status/PeerReviewed | en_US |
dspace.orderedauthors | Ma, D. K.; Rothe, M.; Zheng, S.; Bhatla, N.; Pender, C. L.; Menzel, R.; Horvitz, H. R. | en_US |
dc.identifier.orcid | https://orcid.org/0000-0001-7092-3079 | |
dc.identifier.orcid | https://orcid.org/0000-0002-9964-9613 | |
dc.identifier.orcid | https://orcid.org/0000-0002-1693-4524 | |
mit.license | PUBLISHER_POLICY | en_US |
mit.metadata.status | Complete | |