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Mechanistic Studies on the Impact of Sleep Deprivation on Gene Regulation

Mechanistic Studies on the Impact of Sleep Deprivation on Gene Regulation
睡眠剥夺对基因调控影响的机制研究
批准号:
10398122
负责人:
EDWIN TED G. ABEL
金额:
$57.79万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
已结题
起止时间:
2019-08-01 至 2024-04-30
关键词:
AcuteAdultAdverse effectsAffectAffinity ChromatographyAgingAlzheimer&aposs DiseaseAmericanAnimalsAreaBehavior ControlBehavioralBiochemicalBiological AssayBrain regionCell NucleusCellsCenters for Disease Control and Prevention (U.S.)ChronicCognition DisordersCognitive deficitsDementiaDevelopmentDiseaseEconomic BurdenEventFRAP1 geneFoundationsFutureGene ExpressionGene Expression RegulationGenetic TranscriptionGenomicsHealthHealth Care CostsHippocampus (Brain)Impaired cognitionImpairmentIn SituIndividualLearningMapsMediatingMemoryMemory impairmentMental disordersMessenger RNAMolecularMolecular TargetNeurodegenerative DisordersNuclearNuclear RNAOccupational AccidentsPathologyPathway interactionsPerformancePersonsPhosphorylationPlant RootsPost-Translational Protein ProcessingProcessProductivityProtein BiosynthesisProtein Synthesis InhibitionProteinsPublic HealthRNARNA ProcessingRNA SplicingRNA TransportRNA-Binding ProteinsRegulationReportingResearchRibosomesSafetySignal PathwaySignal TransductionSleep DeprivationSynapsesSynaptic plasticityTechniquesTechnologyTeenagersTestingTraffic accidentsTranscriptTranslatingTranslationsViralage relatedbasecell typecognitive functioncognitive performancedisorder riskexcitatory neuronhippocampal subregionsimprovedin vivoin vivo evaluationinsightlong term memorymemory processnegative affectnervous system disordernovel therapeuticsoverexpressionregional differencerelating to nervous systemresiliencetherapeutic developmenttherapy developmenttranscriptome sequencing

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Project Summary Sleep deprivation presents an increasing threat to individual health and public safety as well as an economic burden due to lost productivity, traffic accidents, occupational accidents, and skyrocketing healthcare costs. There has been an astonishing rise in the number of individuals affected by sleep deprivation with approximately 35% of U.S. adults and a staggering 70% of teenagers reporting insufficient sleep. Sleep deprivation induces significant impairments in memory and performance, aggravates psychiatric and neurological disorders and increases disease risk, especially neurodegenerative disorders such as Alzheimer’s disease. Given the significant number of people affected by sleep deprivation, and the potentially devastating consequences of sleep loss in terms of disease and dementia, it is essential to identify the cellular consequences of sleep deprivation and to define the specific molecular targets and processes impacted. Recent research suggests that the influence of acute sleep deprivation on memory occurs at the cellular and synaptic level, although the specific mechanisms through which sleep deprivation exerts these effects remain poorly understood. The hippocampus, a critical brain region for memory, is particularly susceptible to the effects of acute sleep deprivation. Previously, we found that sleep deprivation decreases protein synthesis in the hippocampus leading to impairments and deficits in synaptic plasticity. We hypothesize that sleep deprivation targets multiple processes that affect the regulation of gene expression, which is comprised of changes in transcription, RNA processing and localization, and protein synthesis. The objectives of this proposal are to define the molecular and cellular mechanisms through which sleep deprivation impacts gene regulation and to define the affected subregions and cell types within the hippocampus. In Specific Aim 1, we focus on the signaling pathways through which sleep deprivation affects protein synthesis to adversely impact long-term memory and synaptic plasticity with a focus on identifying mechanisms of resilience to sleep loss. In Specific Aim 2, we investigate the effects of sleep deprivation on RNA fate at the subcellular level and explicitly detail the effects of sleep deprivation on the pool of mRNA available for translation. In Specific Aim 3, we employ state of the art techniques to define the impact of sleep deprivation across subregions within the hippocampus and within individual cell types providing a detailed spatial map and cellular signature of the effects of sleep deprivation. The results from our comprehensive proposal integrating in vivo behavioral manipulations to mitigate the effects of sleep deprivation on memory, the subcellular analysis of the effects of sleep deprivation on RNA fate and protein synthesis, and the identification of cell specific signatures of sleep deprivation, will provide significant insights into the negative impacts of sleep deprivation on memory, potentially leading to the development of therapeutics to counteract the consequences of sleep loss on cognition and neurodegenerative disorders.
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University of Iowa Hawkeye Intellectual and Developmental Disabilities Research Center (Hawk-IDDRC)
  • 批准号:
    10451564
  • 项目类别:
  • 资助金额:
    $120.89万
  • 财政年份:
    2021
  • 负责人:
    EDWIN TED G. ABEL
  • 依托单位:
University of Iowa Hawkeye Intellectual and Developmental Disabilities Research Center (Hawk-IDDRC)
  • 批准号:
    10238630
  • 项目类别:
  • 资助金额:
    $123.02万
  • 财政年份:
    2021
  • 负责人:
    EDWIN TED G. ABEL
  • 依托单位:
Core A: Administrative Core
  • 批准号:
    10451565
  • 项目类别:
  • 资助金额:
    $24.29万
  • 财政年份:
    2021
  • 负责人:
    EDWIN TED G. ABEL
  • 依托单位:
Core A: Administrative Core
  • 批准号:
    10669136
  • 项目类别:
  • 资助金额:
    $24.29万
  • 财政年份:
    2021
  • 负责人:
    EDWIN TED G. ABEL
  • 依托单位:
海外基金