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dc.contributor.authorYelin-Bekerman, Laura
dc.contributor.authorElbaz, Idan
dc.contributor.authorDiber, Alex
dc.contributor.authorDahary, Dvir
dc.contributor.authorGibbs-Bar, Liron
dc.contributor.authorAlon, Shahar
dc.contributor.authorLerer-Goldshtein, Tali
dc.contributor.authorAppelbaum, Lior
dc.date.accessioned2015-11-02T20:15:29Z
dc.date.available2015-11-02T20:15:29Z
dc.date.issued2015-10
dc.identifier.issn2050-084X
dc.identifier.urihttp://hdl.handle.net/1721.1/99667
dc.description.abstractSleep has been conserved throughout evolution; however, the molecular and neuronal mechanisms of sleep are largely unknown. The hypothalamic hypocretin/orexin (Hcrt) neurons regulate sleep/wake states, feeding, stress, and reward. To elucidate the mechanism that enables these various functions and to identify sleep regulators, we combined fluorescence cell sorting and RNA-seq in hcrt:EGFP zebrafish. Dozens of Hcrt-neuron-specific transcripts were identified and comprehensive high-resolution imaging revealed gene-specific localization in all or subsets of Hcrt neurons. Clusters of Hcrt-neuron-specific genes are predicted to be regulated by shared transcription factors. These findings show that Hcrt neurons are heterogeneous and that integrative molecular mechanisms orchestrate their diverse functions. The voltage-gated potassium channel Kcnh4a, which is expressed in all Hcrt neurons, was silenced by the CRISPR-mediated gene inactivation system. The mutant kcnh4a(kcnh4a-/-) larvae showed reduced sleep time and consolidation, specifically during the night, suggesting that Kcnh4a regulates sleep.en_US
dc.description.sponsorshipUnited States-Israel Binational Science Foundation (Grant 2011335)en_US
dc.description.sponsorshipIsrael Science Foundation (Grant 366/11)en_US
dc.description.sponsorshipIsrael Science Foundation (Legacy Heritage Biomedical Program Grant 398/11)en_US
dc.description.sponsorshipIsrael Science Foundation (Legacy Heritage Biomedical Program Grant 992/14)en_US
dc.description.sponsorshipEuropean Community. Marie-Curie Research Networks (International Reintegration Grant FP7-PEOPLE-2010-RG274333)en_US
dc.language.isoen_US
dc.publishereLife Sciences Publications, Ltd.en_US
dc.relation.isversionofhttp://dx.doi.org/10.7554/eLife.08638en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.sourceeLife Sciences Publications, Ltd.en_US
dc.titleHypocretin neuron-specific transcriptome profiling identifies the sleep modulator Kcnh4aen_US
dc.typeArticleen_US
dc.identifier.citationYelin-Bekerman, Laura, Idan Elbaz, Alex Diber, Dvir Dahary, Liron Gibbs-Bar, Shahar Alon, Tali Lerer-Goldshtein, and Lior Appelbaum. “Hypocretin Neuron-Specific Transcriptome Profiling Identifies the Sleep Modulator Kcnh4a.” eLife 4 (October 1, 2015).en_US
dc.contributor.departmentMassachusetts Institute of Technology. Media Laboratoryen_US
dc.contributor.departmentProgram in Media Arts and Sciences (Massachusetts Institute of Technology)en_US
dc.contributor.mitauthorAlon, Shaharen_US
dc.relation.journaleLifeen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dspace.orderedauthorsYelin-Bekerman, Laura; Elbaz, Idan; Diber, Alex; Dahary, Dvir; Gibbs-Bar, Liron; Alon, Shahar; Lerer-Goldshtein, Tali; Appelbaum, Lioren_US
dc.identifier.orcidhttps://orcid.org/0000-0002-7168-7001
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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