dc.contributor.author | Yelin-Bekerman, Laura | |
dc.contributor.author | Elbaz, Idan | |
dc.contributor.author | Diber, Alex | |
dc.contributor.author | Dahary, Dvir | |
dc.contributor.author | Gibbs-Bar, Liron | |
dc.contributor.author | Alon, Shahar | |
dc.contributor.author | Lerer-Goldshtein, Tali | |
dc.contributor.author | Appelbaum, Lior | |
dc.date.accessioned | 2015-11-02T20:15:29Z | |
dc.date.available | 2015-11-02T20:15:29Z | |
dc.date.issued | 2015-10 | |
dc.identifier.issn | 2050-084X | |
dc.identifier.uri | http://hdl.handle.net/1721.1/99667 | |
dc.description.abstract | Sleep 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.sponsorship | United States-Israel Binational Science Foundation (Grant 2011335) | en_US |
dc.description.sponsorship | Israel Science Foundation (Grant 366/11) | en_US |
dc.description.sponsorship | Israel Science Foundation (Legacy Heritage Biomedical Program Grant 398/11) | en_US |
dc.description.sponsorship | Israel Science Foundation (Legacy Heritage Biomedical Program Grant 992/14) | en_US |
dc.description.sponsorship | European Community. Marie-Curie Research Networks (International Reintegration Grant FP7-PEOPLE-2010-RG274333) | en_US |
dc.language.iso | en_US | |
dc.publisher | eLife Sciences Publications, Ltd. | en_US |
dc.relation.isversionof | http://dx.doi.org/10.7554/eLife.08638 | en_US |
dc.rights | Creative Commons Attribution | en_US |
dc.rights.uri | http://creativecommons.org/licenses/by/4.0/ | en_US |
dc.source | eLife Sciences Publications, Ltd. | en_US |
dc.title | Hypocretin neuron-specific transcriptome profiling identifies the sleep modulator Kcnh4a | en_US |
dc.type | Article | en_US |
dc.identifier.citation | Yelin-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.department | Massachusetts Institute of Technology. Media Laboratory | en_US |
dc.contributor.department | Program in Media Arts and Sciences (Massachusetts Institute of Technology) | en_US |
dc.contributor.mitauthor | Alon, Shahar | en_US |
dc.relation.journal | eLife | en_US |
dc.eprint.version | Final published version | 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 | Yelin-Bekerman, Laura; Elbaz, Idan; Diber, Alex; Dahary, Dvir; Gibbs-Bar, Liron; Alon, Shahar; Lerer-Goldshtein, Tali; Appelbaum, Lior | en_US |
dc.identifier.orcid | https://orcid.org/0000-0002-7168-7001 | |
mit.license | PUBLISHER_CC | en_US |
mit.metadata.status | Complete | |