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中文摘要
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描述(由申请人提供):情景记忆包括自传式经历,这些经历可以被有意识地回忆起来。包括海马体在内的内侧颞叶区域通常被认为是控制情景记忆形成的关键大脑区域,这些区域的退化,如阿尔茨海默病,通常与记忆丧失有关。尽管记忆在健康和疾病中都扮演着重要的角色,但人们对决定人类记忆表现差异的基因知之甚少。为了确定影响记忆的遗传因素,我们对瑞士国籍的个体进行了全基因组关联研究,该研究基于记忆表现分层。位于KIBRA基因中的SNP rs17070145被发现与记忆表现显著相关,并随后在两个独立的队列中得到验证。表达分析表明,KIBRA转录本在海马中富集,功能性MRI研究显示,非rs17070145t等位基因携带者在记忆检索过程中增加了海马的激活。这些数据表明,KIBRA在情景记忆的形成中起着至关重要的作用,并导致了一种假设,即在记忆表现较差的个体中存在KIBRA的变体。本研究计划的目标是确定这种变异并确定其对KIBRA的影响。这将通过研究相关单倍型的生物学相关snp,识别海马中表达KIBRA的细胞并比较单倍型阴性和阳性个体的差异,通过检查KIBRA生物学途径的体内抑制剂来调节记忆影响,以及通过基因转移改变海马体中KIBRA的表达水平来实现。拟议的研究将导致对记忆生物学的更全面的理解,并希望利用这些信息为那些患有健忘症的人开发保留记忆的药物。以记忆丧失为症状的疾病是常见且具有破坏性的。我们目前对记忆过程的工作原理了解甚少。这项研究计划的目标是扩展一项基因发现,将一种被称为KIBRA的蛋白质与记忆表现联系起来,以更好地理解它在记忆过程中的作用,希望不仅能进一步增进我们的知识,还能开发出新的药物,以保护患有阿尔茨海默氏症等遗忘性疾病的人的记忆功能。
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)
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科研奖励(0)
会议论文
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
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
Immune and inflammatory system changes in SuperAgers
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: