Identification of Synaptic remodeling Genes in C. elegans
Identification of Synaptic remodeling Genes in C. elegans
批准号:
7083977
负责人:
DAVID M MILLER
金额:
$21.54万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-05-01 至 2008-04-30
关键词:
Caenorhabditis elegansRNA interferenceaxoncellular polaritydendritesdevelopmental geneticsdevelopmental neurobiologygamma aminobutyrategene expression profilinggene mutationgreen fluorescent proteinshelminth geneticslarvametamorphosismicroarray technologymotor neuronsneural plasticityneurotransmitter receptorsteroid hormone receptorsynaptogenesistranscription factor
中文摘要
描述(申请者提供):在神经系统中,突触输入和输出的模式决定了信息流动的方向。神经元通过称为树突的细长过程检测刺激,并从形态上不同的一类细胞质延伸(称为轴突)释放信号。神经元的这些不对称特征是受发育控制的,对大脑功能至关重要。在线虫C. elegans中,DD类GABA运动神经元经历了发育调节的突触极性逆转,其中树突转变为轴突,轴突采用树突的特性。值得注意的是,DD神经元过程并没有被撤回来适应这种变化,而是在原位进行了重塑,以相互转换突触前和突触后的特化。该程序的实施受UNC- 55的调控,UNC- 55是核激素受体转录因子COUP家族的保守成员。因此,我们假设DD运动神经元的极性反转和突触重塑是受转录控制的。我们将使用新的、强大的、细胞特异性的微阵列技术来(1)分析发育期间发生变态的DD运动神经元;(2)利用unc-55突变体来鉴定unc-55调控的转录物。这些数据集的比较应该揭示强有力的候选基因,协调极性反转和随后的突触重塑的DD运动神经元。脊椎动物神经元不对称的明显可塑性和指定神经元极性的分子的进化守恒表明,我们在线虫模型系统中的发现将揭示在调节这些事件中起基本作用的基因。
英文摘要
DESCRIPTION (provided by applicant): In the nervous system, the pattern of synaptic inputs and outputs defines the direction of information flow. A neuron detects stimuli via elongated processes called dendrites and releases signals from a morphologically distinct class of cytoplasmic extensions called axons. These asymmetric features of neurons are developmentally controlled and fundamentally important to brain function. In the nematode, C. elegans, the DD class of GABA motor neurons undergoes a developmentally regulated reversal of synaptic polarity in which a dendrite switches to become an axon and an axon adopts the properties of a dendrite. Remarkably, DD neuronal processes are not withdrawn to accommodate this change but are remodeled in situ to interconvert pre- and post-synaptic specializations. The implementation of this program is regulated by UNC- 55, a conserved member of the COUP family of nuclear hormone receptor transcription factors. Therefore, we hypothesize that polarity reversal and synaptic remodeling of the DD motor neurons are transcriptionally controlled. We will use new, powerful, cell-specific microarray technology to (1) profile DD motor neurons during the developmental period in which metamorphosis occurs and (2) exploit unc-55 mutants to identify UNC-55 regulated transcripts. A comparison of these data sets should reveal strong candidates for genes that orchestrate polarity reversal and the consequent synaptic remodeling of DD motor neurons. The evident plasticity of vertebrate neuronal asymmetry and the evolutionary conservation of molecules that specify neuronal polarity suggest that our discoveries in a nematode model system will reveal genes with fundamental roles in regulating these events.
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