Epitranscriptomic mechanisms of fear-related learning and memory
Epitranscriptomic mechanisms of fear-related learning and memory
批准号:
9261601
负责人:
Robert C Spitale
金额:
$37.64万
依托单位国家:
美国
项目类别:
财政年份:
2016
资助国家:
美国
项目状态:
已结题
起止时间:
2016-04-15 至 2021-01-31
关键词:
AddressAdultAffectAutomobile DrivingBehavioralBehavioral ParadigmBinding ProteinsBiological AssayBiologyBrainCellsCharacteristicsDNA SequenceDataEnsureEnvironmentEpigenetic ProcessExtinction (Psychology)FrightGene ExpressionGene Expression ProfilingGene Expression RegulationGenesGoalsHeritabilityHigh-Throughput Nucleotide SequencingImpairmentLaboratoriesLeadLearningLightLongevityMaintenanceMediatingMedicineMemoryMetabolismModificationMolecularNatureNeuronsPathway interactionsPatternPositioning AttributePost-Transcriptional RegulationPre-Clinical ModelProcessProtocols documentationRNARNA StabilityRNA methylationRNA-Binding ProteinsRecording of previous eventsResearchResearch ProposalsRoleStructureTherapeutic InterventionTimeTrainingVariantViralanxiety-related disordersclassical conditioningcognitive functiondemethylationdesigneffective therapyepigenetic regulationexperienceexperimental studyin vivoinnovationinsightknock-downlentiviral-mediatedneuropsychiatric disordernovelprogramspublic health relevancetargeted treatmenttranscriptome
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): RNA modification, and N6 methyladenosine (m6A) in particular, is a newly discovered epigenetic mechanism in the adult brain that is has recently been shown to be highly dynamic and, as indicated by our preliminary evidence, appears to be involved in fear-related learning and memory. The overarching goal of this research program is to establish, for the first time, a causal relationship between the epitranscriptomic regulation of
gene expression and the formation and maintenance of memory in a preclinical model of fear-related anxiety disorder. We can then capitalize on this information to design better treatments for neuropsychiatric disorders characterized by impairments in cognitive function. Successful completion of these experiments also has the potential to dramatically change the way we think about mechanisms of adaptive plasticity by shedding new light on how the qualitative nature of RNA, rather than its overall abundance, is involved in a key learning process with implications for our understanding of neuropsychiatric disorders characterized by abnormally intense memories. This will be achieved through a potent combination of advance high-throughput sequencing approaches, robust behavioral paradigms and viral-mediated manipulation of gene activity in the adult brain.
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依托单位:
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