TOWARDS THE COMPLETE CHARACTERIZATION OF NEUREXIN TRANS-SYNAPTIC LIGANDS
TOWARDS THE COMPLETE CHARACTERIZATION OF NEUREXIN TRANS-SYNAPTIC LIGANDS
批准号:
8365894
负责人:
ANIRVAN GHOSH
金额:
$0.74万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-09-01 至 2012-06-30
关键词:
AdhesionsAlternative SplicingBehaviorBiologyBrainCodeFundingFungal GenomeGenesGrantLigandsNational Center for Research ResourcesNeuronsOrganismPrincipal InvestigatorProtein IsoformsProteinsProteomeResearchResearch InfrastructureResourcesSourceSynapsesUnited States National Institutes of Healthcostneural circuitpresynapticpromoterprotein expression
中文摘要
这个子项目是利用资源的许多研究子项目之一。
由NIH/NCRR资助的中心拨款提供。对子项目的主要支持
子项目的首席调查员可能是由其他来源提供的,
包括美国国立卫生研究院的其他来源。为子项目列出的总成本可能
表示该子项目使用的中心基础设施的估计数量,
不是由NCRR赠款提供给次级项目或次级项目工作人员的直接资金。
跨突触黏附蛋白质组的鉴定和鉴定可能足以破解突触密码。跨突触黏附蛋白质组的测定可能被证明是我们最终理解神经元突触电路和脑连接以及反过来生物体行为的核心。从历史上看,Neurexins(NRXns)被认为是最有可能导致突触后分化的突触前蛋白。NRXN蛋白的表达受到高度调控(3个基因、不同的启动子和大量的不同剪接),有人认为NRXN在哺乳动物的大脑中可能以数千种不同的形式存在。
英文摘要
This subproject is one of many research subprojects utilizing the resources
provided by a Center grant funded by NIH/NCRR. Primary support for the subproject
and the subproject's principal investigator may have been provided by other sources,
including other NIH sources. The Total Cost listed for the subproject likely
represents the estimated amount of Center infrastructure utilized by the subproject,
not direct funding provided by the NCRR grant to the subproject or subproject staff.
The identification and characterization of the trans-synaptic adhesion proteome may prove sufficient to break the synapse code. Determination of the trans-synaptic adhesion proteome may prove central to our eventual understanding of neuronal synaptic circuitry and brain wiring and in turn organism behavior. Historically, Neurexins (NRXNs) have been considered the most-likely presynaptic protein responsible for post-synaptic differentiation. NRXN protein expression is highly regulated (3 genes, alternative promoters, and massive alternative splicing) and it has been proposed that NRXNs may be present in thousands of isoforms within the mammalian brain.
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