Publication:
The after-hours circadian mutant has reduced phenotypic plasticity in behaviors at multiple timescales and in sleep homeostasis

dc.contributor.coauthorMaggi, Silvia
dc.contributor.coauthorBalzani, Edoardo
dc.contributor.coauthorLassi, Glenda
dc.contributor.coauthorGarcia-Garcia, Celina
dc.contributor.coauthorPlano, Andrea
dc.contributor.coauthorEspinoza, Stefano
dc.contributor.coauthorMus, Liudmila
dc.contributor.coauthorTinarelli, Federico
dc.contributor.coauthorNolan, Patrick M.
dc.contributor.coauthorGainetdinov, Raul R.
dc.contributor.coauthorNieus, Thierry
dc.contributor.coauthorTucci, Valter
dc.contributor.departmentDepartment of Psychology
dc.contributor.kuauthorBalcı, Fuat
dc.contributor.kuprofileFaculty Member
dc.contributor.otherDepartment of Psychology
dc.contributor.schoolcollegeinstituteCollege of Social Sciences and Humanities
dc.contributor.yokid51269
dc.date.accessioned2024-11-09T13:52:33Z
dc.date.issued2017
dc.description.abstractCircadian clock is known to adapt to environmental changes and can significantly influence cognitive and physiological functions. In this work, we report specific behavioral, cognitive, and sleep homeostatic defects in the after hours (Afh) circadian mouse mutant, which is characterized by lengthened circadian period. We found that the circadian timing irregularities in Afh mice resulted in higher interval timing uncertainty and suboptimal decisions due to incapability of processing probabilities. Our phenotypic observations further suggested that Afh mutants failed to exhibit the necessary phenotypic plasticity for adapting to temporal changes at multiple time scales (seconds-to-minutes to circadian). These behavioral effects of Afh mutation were complemented by the specific disruption of the Per/Cry circadian regulatory complex in brain regions that govern food anticipatory behaviors, sleep, and timing. We derive statistical predictions, which indicate that circadian clock and sleep are complementary processes in controlling behavioral/cognitive performance during 24 hrs. The results of this study have pivotal implications for understanding how the circadian clock modulates sleep and behavior.
dc.description.fulltextYES
dc.description.indexedbyWoS
dc.description.indexedbyScopus
dc.description.indexedbyPubMed
dc.description.openaccessYES
dc.description.publisherscopeInternational
dc.description.sponsoredbyTubitakEuN/A
dc.description.sponsorshipRussian Science Foundation
dc.description.versionPublisher version
dc.description.volume7
dc.formatpdf
dc.identifier.doi10.1038/s41598-017-18130-2
dc.identifier.eissn2045-2322
dc.identifier.embargoNO
dc.identifier.filenameinventorynoIR01491
dc.identifier.linkhttps://doi.org/10.1038/s41598-017-18130-2
dc.identifier.quartileQ2
dc.identifier.scopus2-s2.0-85038624243
dc.identifier.urihttps://hdl.handle.net/20.500.14288/3986
dc.identifier.wos418359600015
dc.keywordsGene-expression
dc.keywordsPeriod
dc.keywordsMice
dc.keywordsReveals
dc.keywordsRhythms
dc.keywordsDisease
dc.keywordsProtein
dc.keywordsMouse
dc.keywordsFbxl3
dc.keywordsTime
dc.languageEnglish
dc.publisherNature Publishing Group (NPG)
dc.relation.grantno14-50-00069
dc.relation.urihttp://cdm21054.contentdm.oclc.org/cdm/ref/collection/IR/id/8067
dc.sourceScientific Reports
dc.subjectMultidisciplinary sciences
dc.titleThe after-hours circadian mutant has reduced phenotypic plasticity in behaviors at multiple timescales and in sleep homeostasis
dc.typeJournal Article
dspace.entity.typePublication
local.contributor.authorid0000-0003-3390-9352
local.contributor.kuauthorBalcı, Fuat
relation.isOrgUnitOfPublicationd5fc0361-3a0a-4b96-bf2e-5cd6b2b0b08c
relation.isOrgUnitOfPublication.latestForDiscoveryd5fc0361-3a0a-4b96-bf2e-5cd6b2b0b08c

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