Genetic Variation in KIBRA and its role in Human Episodic Memory
Genetic Variation in KIBRA and its role in Human Episodic Memory
批准号:
8049124
负责人:
Matt Huentelman
金额:
$33.6万
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-04-01 至 2013-03-31
关键词:
AffectAging-Related ProcessAllelesAlzheimer&aposs DiseaseAlzheimer&aposs disease riskAnimalsAttentionBiologicalBiologyBrain regionCellsDataDiseaseEnhancersEpisodic memoryFunctional Magnetic Resonance ImagingGene ProteinsGene TransferGenesGeneticGenetic VariationGoalsHaplotypesHealthHippocampus (Brain)HumanIn VitroIndividualIndividual DifferencesInvestigationKnowledgeLeadLinkLittle&aposs DiseaseMeasurementMedialMemoryMemory LossMethodsMusNationalitiesPathway interactionsPatientsPerformancePeripheralPharmaceutical PreparationsPharmacologic SubstancePlayPrefrontal CortexProcessProteinsResearchRetrievalRodentRoleShort-Term MemorySwitzerlandSymptomsTemporal LobeTherapeutic InterventionTranscriptUnited StatesVariantage groupagedaging hippocampusbasecell typecohortcollegeepisodic memory impairmentexecutive functionexperiencegenetic variantgenome wide association studyin vivoinhibitor/antagonistmemory processmemory retrievalmiddle agenormal aging
中文摘要
点击翻译按钮获取中文摘要
英文摘要
DESCRIPTION (provided by applicant): Episodic memory includes autobiographical experiences that are consciously recalled as desired. Regions of the medial temporal lobe, including the hippocampus, are generally considered to be the key brain regions controlling episodic memory formation, and the degeneration of these regions, such as during Alzheimer's disease, is often associated with memory loss. Despite memory's important role in both health and disease, little is known about the genetics that determine the differences in memory performance in humans. To identify genetic factors influencing memory we performed a whole-genome association study on individuals of Swiss nationality stratified based upon memory performance. SNP rs17070145, located in the gene KIBRA, was found to be significantly associated with memory performance and was subsequently validated in two independent cohorts. Expression analysis indicated that KIBRA transcripts were enriched in the hippocampus, and functional MRI investigation showed that non-carriers of the rs17070145 T allele increased activation of the hippocampus during memory retrieval. These data suggest a crucial role for KIBRA in episodic memory formation and leads to the hypothesis that a variant of KIBRA exists in individuals with lowered memory performance. The goal of this research plan is to identify this variant and determine its impact on KIBRA. This will be achieved by investigating SNPs of biological relevance on the associated haplotype, identifying those cells in the hippocampus that express KIBRA and compare haplotype negative and positive individuals for differences, by examining in vivo inhibitors of the KIBRA biological pathways for memory modulating affects, and by altering the expression levels of KIBRA within the hippocampus through gene transfer. The proposed studies will lead to a more complete understanding of the biology of memory with the hope of leveraging this information to develop memory-sparing pharmaceuticals for those individuals suffering from amnestic disease. PUBLIC HEALTH RELEVANCE Diseases with memory loss as a symptom are common and devastating. We currently understand very little about how the process of memory works. The goal of this research plan is to expand upon a genetic finding linking a protein known as KIBRA to memory performance to better understand its role in the process of memory with the hopes of not only furthering our knowledge but also developing new drugs to preserve memory function in individuals suffering from amnestic diseases like Alzheimer's.
期刊论文(9)
专著(0)
科研奖励(0)
会议论文
登录
查看更多内容
DOI:
10.1037/a0014260
发表时间:
2009-02
期刊:
BEHAVIORAL NEUROSCIENCE
影响因子:
1.9
作者:
[Huentelman, Matthew J., Stephan, Dietrich A., Talboom, Joshua, Corneveaux, Jason J., Reiman, David A., Gerber, Jill D., Barnes, Carol A., Alexander, Gene E., Reiman, Eric M., Bimonte-Nelson, Heather A.]
通讯作者:
Bimonte-Nelson, Heather A.
DOI:
10.1016/j.bbr.2011.07.008
发表时间:
2011-11-20
期刊:
BEHAVIOURAL BRAIN RESEARCH
影响因子:
2.7
作者:
[Gunn, Rhian K., Huentelman, Matthew J., Brown, Richard E.]
通讯作者:
Brown, Richard E.
DOI:
10.1111/jnc.12480
发表时间:
2014-03
期刊:
Journal of neurochemistry
影响因子:
4.7
作者:
[Vogt-Eisele A, Krüger C, Duning K, Weber D, Spoelgen R, Pitzer C, Plaas C, Eisenhardt G, Meyer A, Vogt G, Krieger M, Handwerker E, Wennmann DO, Weide T, Skryabin BV, Klugmann M, Pavenstädt H, Huentelmann MJ, Kremerskothen J, Schneider A]
通讯作者:
Schneider A
DOI:
10.1016/j.jalz.2011.11.006
发表时间:
2012-11
期刊:
Alzheimer's & dementia : the journal of the Alzheimer's Association
影响因子:
--
作者:
[Caselli RJ, Dueck AC, Huentelman MJ, Lutz MW, Saunders AM, Reiman EM, Roses AD]
通讯作者:
Roses AD
DOI:
10.1371/journal.pone.0198256
发表时间:
2018
期刊:
PloS one
影响因子:
3.7
作者:
[Willeman MN, Mennenga SE, Siniard AL, Corneveaux JJ, De Both M, Hewitt LT, Tsang CWS, Caselli J, Braden BB, Bimonte-Nelson HA, Huentelman MJ]
通讯作者:
Huentelman MJ
Molecular Profiling (MP) Core G
-
批准号:10491870
-
项目类别:
-
资助金额:$294.17万
-
财政年份:2021
-
负责人:Matt Huentelman
-
依托单位:
Microglia contribution to disease pathogenesis in C9orf72 ALS/FTD
-
批准号:10675015
-
项目类别:
-
资助金额:$80.56万
-
财政年份:2021
-
负责人:Matt Huentelman
-
依托单位:
Immune and inflammatory system changes in SuperAgers
-
批准号:10276528
-
项目类别:
-
资助金额:$71.17万
-
财政年份:2021
-
负责人:Matt Huentelman
-
依托单位:
Project 1: MindCrowd: Precision Aging Cognitive Assessment Through a Web-based Network
-
批准号:10491872
-
项目类别:
-
资助金额:$69.37万
-
财政年份:2021
-
负责人:Matt Huentelman
-
依托单位:
Project 1: MindCrowd: Precision Aging Cognitive Assessment Through a Web-based Network
-
批准号:10689320
-
项目类别:
-
资助金额:$69.37万
-
财政年份:2021
-
负责人:Matt Huentelman
-
依托单位:
Immune and inflammatory system changes in SuperAgers
-
批准号:10687274
-
项目类别:
-
资助金额:$34.52万
-
财政年份:2021
-
负责人:Matt Huentelman
-
依托单位:
Molecular Profiling (MP) Core G
-
批准号:10689317
-
项目类别:
-
资助金额:$293.22万
-
财政年份:2021
-
负责人:Matt Huentelman
-
依托单位:
Molecular Profiling (MP) Core G
-
批准号:10270194
-
项目类别:
-
资助金额:$294.17万
-
财政年份:2021
-
负责人:Matt Huentelman
-
依托单位:
Project 1: MindCrowd: Precision Aging Cognitive Assessment Through a Web-based Network
-
批准号:10270195
-
项目类别:
-
资助金额:$126.37万
-
财政年份:2021
-
负责人:Matt Huentelman
-
依托单位:
Identification of pathogenic mechanisms important in multiple system atrophy
-
批准号:9130283
-
项目类别:
-
资助金额:$13.95万
-
财政年份:2015
-
负责人:Matt Huentelman
-
依托单位:
Identification of pathogenic mechanisms important in multiple system atrophy
-
批准号:8955003
-
项目类别:
-
资助金额:$40.36万
-
财政年份:2015
-
负责人:Matt Huentelman
-
依托单位:
APOEomic: Searching for APOE interacting risk factors using omics data
-
批准号:8439407
-
项目类别:
-
资助金额:$35.9万
-
财政年份:2013
-
负责人:Matt Huentelman
-
依托单位:
APOEomic: Searching for APOE interacting risk factors using omics data
-
批准号:8923140
-
项目类别:
-
资助金额:$33.75万
-
财政年份:2013
-
负责人:Matt Huentelman
-
依托单位:
Genetic Variation in KIBRA and its role in Human Episodic Memory
-
批准号:7599012
-
项目类别:
-
资助金额:$34.25万
-
财政年份:2008
-
负责人:Matt Huentelman
-
依托单位:
Genetic Variation in KIBRA and its role in Human Episodic Memory
-
批准号:7464992
-
项目类别:
-
资助金额:$35.6万
-
财政年份:2008
-
负责人:Matt Huentelman
-
依托单位:
Genetic Variation in KIBRA and its role in Human Episodic Memory
-
批准号:7799254
-
项目类别:
-
资助金额:$33.88万
-
财政年份:2008
-
负责人:Matt Huentelman
-
依托单位: