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dc.contributor.authorRush, Brandy L.
dc.contributor.authorMurad, Alejandro D.
dc.contributor.authorEmery, Patrick
dc.contributor.authorGiebultowicz, Jadwiga M.
dc.date2022-08-11T08:08:47.000
dc.date.accessioned2022-08-23T16:08:36Z
dc.date.available2022-08-23T16:08:36Z
dc.date.issued2006-07-26
dc.date.submitted2008-12-09
dc.identifier.citationJ Biol Rhythms. 2006 Aug;21(4):272-8. <a href="http://dx.doi.org/10.1177/0748730406290416">Link to article on publisher's site</a>
dc.identifier.issn0748-7304 (Print)
dc.identifier.doi10.1177/0748730406290416
dc.identifier.pmid16864647
dc.identifier.urihttp://hdl.handle.net/20.500.14038/32487
dc.description.abstractThe period (per) and timeless (tim) genes play a central role in the Drosophila circadian clock mechanism. PERIOD (PER) and TIMELESS (TIM) proteins periodically accumulate in the nuclei of pace-making cells in the fly brain and many cells in peripheral organs. In contrast, TIM and PER in the ovarian follicle cells remain cytoplasmic and do not show daily oscillations in their levels. Moreover, TIM is not light sensitive in the ovary, while it is highly sensitive to this input in circadian tissues. The mechanism underlying this intriguing difference is addressed here. It is demonstrated that the circadian photoreceptor CRYPTOCHROME (CRY) is not expressed in ovarian tissues. Remarkably, ectopic cry expression in the ovary is sufficient to cause degradation of TIM after exposure to light. In addition, PER levels are reduced in response to light when CRY is present, as observed in circadian cells. Hence, CRY is the key component of the light input pathway missing in the ovary. However, the factors regulating PER and TIM levels downstream of light/cry action appear to be present in this non-circadian organ.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=16864647&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1177/0748730406290416
dc.subjectAnimals; Animals, Genetically Modified; Biological Clocks; Circadian Rhythm; Drosophila Proteins; Drosophila melanogaster; Eye Proteins; Female; *Light; Nuclear Proteins; Ovarian Follicle; Receptors, G-Protein-Coupled
dc.subjectNeuroscience and Neurobiology
dc.titleEctopic CRYPTOCHROME renders TIM light sensitive in the Drosophila ovary
dc.typeJournal Article
dc.source.journaltitleJournal of biological rhythms
dc.source.volume21
dc.source.issue4
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_sp/1056
dc.identifier.contextkey678821
html.description.abstract<p>The period (per) and timeless (tim) genes play a central role in the Drosophila circadian clock mechanism. PERIOD (PER) and TIMELESS (TIM) proteins periodically accumulate in the nuclei of pace-making cells in the fly brain and many cells in peripheral organs. In contrast, TIM and PER in the ovarian follicle cells remain cytoplasmic and do not show daily oscillations in their levels. Moreover, TIM is not light sensitive in the ovary, while it is highly sensitive to this input in circadian tissues. The mechanism underlying this intriguing difference is addressed here. It is demonstrated that the circadian photoreceptor CRYPTOCHROME (CRY) is not expressed in ovarian tissues. Remarkably, ectopic cry expression in the ovary is sufficient to cause degradation of TIM after exposure to light. In addition, PER levels are reduced in response to light when CRY is present, as observed in circadian cells. Hence, CRY is the key component of the light input pathway missing in the ovary. However, the factors regulating PER and TIM levels downstream of light/cry action appear to be present in this non-circadian organ.</p>
dc.identifier.submissionpathgsbs_sp/1056
dc.contributor.departmentMorningside Graduate School of Biomedical Sciences
dc.contributor.departmentEmery Lab
dc.contributor.departmentNeurobiology
dc.source.pages272-8
dc.contributor.studentAlejandro Murad
dc.description.thesisprogramNeuroscience


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