Epigenetic regulation of the circadian gene Per1 in age-related memory impairments
Epigenetic regulation of the circadian gene Per1 in age-related memory impairments
批准号:
10002164
负责人:
JANINE LYNN KWAPIS
金额:
$24.9万
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:
2019-09-01 至 2022-05-31
关键词:
AffectAgeAge-associated memory impairmentAgingAlzheimer&aposs DiseaseAmericanAnimalsCREBBP geneCaliforniaChromatin StructureCircadian DysregulationCircadian RhythmsClustered Regularly Interspaced Short Palindromic RepeatsCollaborationsDataDeacetylaseDevelopmentDevelopment PlansDiseaseDorsalEngineeringEnvironmentEpigenetic ProcessFoundationsFunctional disorderFundingFutureGene ExpressionGene Expression RegulationGenesGeneticGenetic EngineeringGenetic TranscriptionGoalsGrantHDAC3 geneHippocampus (Brain)Histone AcetylationImpaired cognitionImpairmentIndividualInstitutionInterventionJob ApplicationLaboratoriesLeadLearningLinkMediatingMemoryMemory impairmentMolecularMolecular BiologyMusPeriodicityPlayPopulationPositioning AttributeProcessRegulationRepressionResearchResearch PersonnelRoleScientistSiteSmall Interfering RNATechnical ExpertiseTechnologyTestingTimeTrainingUniversitiesVirusWritingage relatedaging brainaging hippocampusbasecareerchromatin immunoprecipitationchromatin remodelingcircadiancircadian pacemakercircadian regulationcognitive functiondesignepigenetic regulationexperienceexperimental studygene repressionhistone acetyltransferasehistone modificationjuvenile animalknock-downlong term memorymemory consolidationmild cognitive impairmentmutantneuromechanismnormal agingnovelnovel therapeuticsoverexpressionpreventprogramspromoterprotein protein interactionremediationskillstranscriptome sequencingtreatment strategy
中文摘要
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英文摘要
Project Summary/Abstract
Alzheimer's Disease affects 5.4 million Americans [1] and by 2030, approximately 13.8 million people 65 or
older are projected to have the disease [2]. Even more individuals will experience normal age-related cognitive
decline, mild cognitive impairment, and impairments in long-term memory formation. It is therefore critical to
understand the mechanisms underlying memory formation in the context of normal age-dependent cognitive
decline. This proposal tests whether Per1 is a key novel mechanism that links aberrant epigenetic
transcriptional repression in the aging brain with age-related impairments in both circadian rhythmicity and
long-term memory formation. First, this proposal will test whether the repressive activity of histone deacetylase
3 (HDAC3) contributes to age-related impairments in both memory formation and gene expression. Next, it will
determine whether Per1 is a mechanism through which HDAC3 limits memory formation in the aging brain.
Finally, using a CRISPR/dCas9-based genetic engineering approach, this project will test whether site-specific
epigenetic manipulations at Per1 can ameliorate age-related impairments in memory formation. Together, the
experiments in this proposal will determine whether epigenetic dysregulation of the circadian gene Per1 in the
dorsal hippocampus contributes to age-related impairments in long-term memory formation.
The proposed project will also help the candidate, Dr. Janine Kwapis, achieve her career goal of becoming
an independent investigator at a research-focused institution. This project provides training in cutting-edge
research skills, including the development and application of CRISPR/dCas9 technology and training in
circadian rhythm research. Further, the proposed studies will lay the foundation for a research program that
extends well beyond the proposed grant. The University of California, Irvine provides an ideal environment for
training the candidate in these new technical skills, with world-renowned experts in memory, aging, circadian
rhythms, and molecular biology. Further, UCI provides an intellectual environment that encourages
collaboration and cooperation, allowing the candidate to grow as a scientist and prepare for a successful
career. In addition to the proposed research, Dr. Kwapis will engage in a number of activities designed to
prepare her to successfully achieve independence, including training in grantsmanship, presentations,
scientific writing, didactic training, job application, and lab management. The systematic plan proposed here
(including both the research plan and the candidate development plan) is calibrated to produce a successful,
independent research scientist who performs unique cutting-edge research that can support a new laboratory
and is well-positioned to receive future R01 funding.
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Diurnal control of memory allocation by the circadian gene Per1
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Epigenetic regulation of the circadian gene Per1 in age-related memory impairments
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