Analysis of the Regulation of G protein-Coupled Sensory Signaling in C. Elegans
Analysis of the Regulation of G protein-Coupled Sensory Signaling in C. Elegans
批准号:
0917896
负责人:
Denise Ferkey
金额:
$74.5万
依托单位:
依托单位国家:
美国
项目类别:
Standard Grant
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-07-01 至 2013-09-30
中文摘要
该奖项是根据2009年美国复苏和再投资法案(公法111-5)资助的。智力价值所有动物都依赖于它们对不断变化的环境做出感知和反应的能力来生存。由于没有眼睛或耳朵,线虫(小型蛔虫)严重依赖其在土壤环境中品尝和嗅觉化学信息的能力来寻找食物和避免危险;动物必须转向指示食物来源的化学物质,同时避免指示潜在有害环境的化学物质。当化学信号(味觉和气味)与感觉神经细胞(神经元)上的蛋白质(受体)结合并启动一系列细胞内事件最终激活神经元时,就会引发这些行为反应。神经元的活动反过来又控制着有机体的行为。尽管这一化学信号转导过程在物种之间高度保守,但我们对用于调节信号的机制的理解仍然存在很大差距。结合强大的遗传和分子工具,线虫是一个理想的模式系统,在其中剖析单个基因和调控途径对整合神经功能和感觉行为的贡献。失去负信号调节因子(秀丽线虫GRK-2)令人惊讶地导致感觉神经元钙信号的减少,并伴随着吸引和回避化学感觉行为的丧失。在缺乏GRK-2的情况下,代偿抑制通路似乎上调,从而抑制信号以保护神经元免受过度刺激。该项目将在一个简单的模型生物体中利用细胞、生化和遗传学方法来了解细胞如何对异常信号做出反应;这些发现将有助于研究从酵母到人类的各种有机体的研究人员。特别是,它们将提供关于受体下游信号和调控通路的互连的有价值的信息。此外,细胞用来补偿错误调节的信号的新机制可能会被揭示。更广泛的影响研究生和本科生,包括女性和少数族裔学生,将参与这些研究。布法罗大学(UB)是一个非常多样化的校园,为指导少数族裔学生提供了一个很好的机会。这笔助学金将为一所本身没有本科生研究的文理学院的本科生提供暑期津贴。提供早期接触假说驱动的研究对于学生为生物科学的职业生涯做准备是至关重要的。学生将在当地(每月)、地区和国际会议上介绍他们的发现。重要的是,一年一度的线虫会议促进了初级科学家的发展,因为许多发言者是从研究生提交的摘要中挑选出来的。这项工作的发现也将包括在亚利桑那大学本科生信号转导课程的讲座中。从该项目的遗传筛查中获得的突变体将被存放在线虫遗传中心,该中心将把它们分发给任何提出请求的研究人员。新的基因和表型描述也将被纳入到在线开放获取资源Wormbase中。
英文摘要
This award is funded under the American Recovery and Reinvestment Act of 2009 (Public Law 111-5).Intellectual MeritAll animals rely on their ability to sense and respond to their constantly changing environments to survive. Because they do not have eyes or ears, C. elegans (small roundworms) depend heavily upon their ability to taste and smell chemical information in their soil environment to find food and avoid danger; animals must move towards chemicals that indicate a food source while avoiding chemicals that indicate potentially harmful environments. These behavioral responses are elicited when the chemical signals (tastants and odorants) bind to proteins (receptors) on sensory nerve cells (neurons) and initiate a chain of intracellular events that ultimately activates the neuron. Neuronal activity, in turn, controls the behavior of the organism. Although this process of chemical signal transduction is highly conserved across species, there are still large gaps in our understanding of the mechanisms used to regulate signaling. Coupled with powerful genetic and molecular tools, C. elegans is an ideal model system in which to dissect the contributions of individual genes and regulatory pathways to integrated neuronal function and sensory behavior. Loss of a negative regulator of signaling (C. elegans GRK-2) surprisingly leads to decreased calcium signaling in sensory neurons and a concomitant loss of both attractive and avoidance chemosensory behaviors. In the absence of GRK-2 there appears to be an upregulation of compensatory inhibitory pathways that dampen signaling to protect neurons from overstimulation. This project will utilize cellular, biochemical and genetic approaches in a simple model organism to understand how cells respond to aberrant signaling; the findings will benefit researchers working in organisms ranging from yeast to humans. In particular, they will provide valuable information on the interconnectedness of signaling and regulatory pathways downstream of receptors. In addition, novel mechanisms used by cells to compensate for mis-regulated signaling may be revealed. Broader ImpactGraduate students and undergraduates, including women and minority students, will participate in these studies. The University at Buffalo (UB) is a very diverse campus, providing a great opportunity to mentor minority students. Funds from this grant will support a summer stipend for an undergraduate from a Liberal Arts College that does not itself have undergraduate research. Providing early exposure to hypothesis-driven research is essential for preparing students for careers in the biological sciences. Students will present their findings at local (monthly), regional and international meetings. Importantly, the annual C. elegans meetings foster the development of junior scientists because many of the speakers are selected from graduate student submitted abstracts. Findings from this work will also be included in the lectures in an undergraduate Signal Transduction course at UB. Mutants obtained from the genetic screens in this project will be deposited at the Caenorhabditis Genetics Center, which will distribute them to any investigator that requests them. New gene and phenotype descriptions will also be incorporated into Wormbase, an online open access resource.
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会议论文
Developmental Specification of a Polymodal Nociceptor in C. elegans
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批准号:1351649
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项目类别:Continuing Grant
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资助金额:$52.5万
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财政年份:2014
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负责人:Denise Ferkey
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依托单位:
海外基金