Investigating Genetics of Human Natural Short Sleepers
Investigating Genetics of Human Natural Short Sleepers
批准号:
8704740
负责人:
YING-HUI FU
金额:
$44.03万
依托单位国家:
美国
项目类别:
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-09-01 至 2016-08-31
关键词:
AffectAlcoholsAmericanAnimal ModelArousalBehaviorBindingBioinformaticsBiologicalCaffeineCandidate Disease GeneCell physiologyCellsCessation of lifeChemicalsChronicCircadian RhythmsCodeCognitionCollectionComplexData SetDisadvantagedDisciplineDiseaseEmploymentEpidemiologyExonsFamilyFoundationsFunctional RNAGene MutationGene StructureGenesGenomeHealthHomeostasisHourHumanHuman GeneticsImmunityIndividualInvestigationInvestmentsKnowledgeLeadLeftLifeLife StyleMaintenanceMassive Parallel SequencingMetabolic syndromeMetabolismMethodsMolecular ProbesMorbidity - disease rateMusMutationOpen Reading FramesOrganismPatient Self-ReportPatternPeriodicityPhenotypePopulationPriceProcessProteinsPublicationsPublishingRegulationReportingResearchResourcesRiskSamplingSchoolsSleepSleep DeprivationSleep DisordersSocietiesSocioeconomic StatusSurveysTechnologyTemperatureTicksTimeUnited States National Institutes of HealthVariantWakefulnessWorkbasecancer riskcircadian pacemakercostcost effectivedietary controlexomeexome sequencingflygenome sequencingimmune functionimprovedmortalitymotor controlnovelprobandscreeningtooltransmission process
中文摘要
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英文摘要
DESCRIPTION (provided by applicant):
Sleep is a global state and its control mechanisms are manifested at every level of biological organization- from genes and intracellular mechanisms, to networks of cell populations, to phenotypes at the organismal level. They include (but are not limited to) arousal, motor control, autonomic function, behavior, and cognition. We live in a sleep deprived society. Prolonged sleep loss impairs temperature control, dietary metabolism, immune function, and eventually leads to death. Sleep deprivation increases an individual's risk of cancer, metabolic syndrome, psychiatric, and other disorders. Understanding the biological basis of sleep in humans is an extremely difficult challenge since the biological determinants of our sleep are affected by behavior and other factors including life-style choices, socio-economic status, health, employment, school, and exogenous chemicals like caffeine and alcohol. Sleep and circadian function are distinct processes that interact in living organisms. Sleep is controlled by at least two processes: a circadian pacemaker (the clock) ticking with periodicity of ~24 hours, and a homeostatic drive that increases during wakefulness and dissipates during sleep. Despite of the fact that we spend around one third of our life in the state of sleep, we understand almost nothing about regulatory mechanisms governing sleep quantity. A unique opportunity presented itself when we identified independent families with a dramatically reduced biological need for sleep. Identification of new subjects and expanding our collection of these families will establish a foundation for us to begin probing the molecular regulatory mechanisms of sleep homeostasis. Recently, we reported the first mutation that causes this short-sleep phenotype. Interestingly, this mutation gave a similar short sleep phenotype in human, mouse, and fly. All the genes identified in this study will therefore become entry points for us to unravel the enigmatic sleep related mechanisms. Ultimately, combining the knowledge from studies in multiple genes and in humans and model organisms will lead to a better understanding of sleep and its relationship to health and disease.
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