G Protein-Mediated Integration of Oxygen Sensing and Energy Balance in C. Elegans
G Protein-Mediated Integration of Oxygen Sensing and Energy Balance in C. Elegans
批准号:
8457362
负责人:
Supriya Srinivasan
金额:
$41.22万
依托单位国家:
美国
项目类别:
财政年份:
2013
资助国家:
美国
项目状态:
已结题
起止时间:
2013-04-01 至 2018-03-31
关键词:
Afferent NeuronsAmericanAnimalsBehavior ControlBiological ModelsBlood CirculationBody fatBrainBrain regionCaenorhabditis elegansCouplesCuesCyclic GMPDataDefectDiabetes MellitusDimensionsEsthesiaEventFatty acid glycerol estersG-Protein-Coupled ReceptorsGTP-Binding ProteinsGenesGeneticGoalsHealthHeart DiseasesHumanInflammationInternationalKnowledgeLaboratoriesLeadLifeLinkLipaseMalignant NeoplasmsMeasuresMediatingMetabolicModalityModelingMolecularMolecular TargetMusNervous system structureNeuronsNeurosecretory SystemsNutrientObesityOrthologous GeneOutcomeOutputOxygenPathway interactionsPerceptionPhysiologicalPlayPositioning AttributeProcessProtein FamilyProteinsPublic HealthRegulationReporterResearchRoleSensorySequence HomologySignal TransductionSiteTestingTissuesTranscriptional ActivationUrsidae FamilyWorkbasecombatdetection of nutrientenergy balanceinsightmembermutantneural circuitneuromechanismneuroregulationnovelpromoterprotein activationpublic health relevancerat Gnat3 proteinreceptor-mediated signalingrelating to nervous systemresearch studyresponse
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英文摘要
DESCRIPTION (provided by applicant): Sensory perception plays an important role in maintaining energy balance and normal body fat content. Despite its significance, there is a major gap in our understanding of the molecular mechanisms that link specific sensory modalities, to energy balance circuits in the brain. Our long-term goal is to identify the molecula mechanisms that integrate sensory signals in the nervous system with intrinsic cues to regulate body fat, and the defects in this process that lead to obesity. The objective of the proposed research is to determine the role of the G¿ protein GPA-8 in C. elegans, a powerful and tractable model system for the study of energy balance circuits. GPA-8 is homologous to the mammalian ¿-gustducin G¿ protein, and is expressed in oxygen-sensing neurons in C. elegans. The central hypothesis of the proposed research is that GPA-8 signaling from sensory neurons integrates oxygen sensing with body fat content. We expect that understanding the mechanism of action of GPA-8 in C. elegans will be a critical step toward identifying the neural circuits and
conserved molecular mechanisms by which oxygen sensation in the nervous system influences body fat content. Our Specific Aims are to: I. Identify the GPA-8-expressing neurons that regulate body fat. Using neuron-specific promoters, we will restore GPA-8 expression in subsets of neurons in gpa-8 mutant animals to define the precise anatomical sites of GPA-8 action in regulating body fat. II. Define the intracellular mode of action for GPA-8. GPA-8 is a G¿ protein suggesting that loss of G protein signaling in oxygen-sensing neurons regulates body fat. We will test the effects of loss of G protein activation cycle genes specifically in oxygen-sensing neurons, to determine the intracellular mode of action of GPA-8. III. Determine the mechanisms of integration of oxygen sensation with fat stores. We will test a candidate genetic pathway involved in cGMP signaling and in oxygen-sensing for changes in body fat under different oxygen concentrations, to delineate the neural mechanisms underlying the integration of oxygen-sensing and body fat content. With respect to expected outcomes, the completion of the proposed work will enable the first insights into the neural circuits and molecular mechanisms that connect oxygen-sensing in the nervous system, with body fat content. Importantly, our findings will allow us to identify signaling paradigms underlying the gut-brain axis that controls energy balance. Because all of the genes under study have clear mammalian orthologs, our contribution here will have a positive impact on rapidly identifying new molecular targets for combating obesity and its associated illnesses. The proposed research is significant because a molecular connection between neural oxygen sensing and body fat content provides a new dimension to our understanding of organismal energy balance and the causes underlying obesity.
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资助金额:$50.96万
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Neuronal Orchestration of Metabolic State and Longevity
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资助金额:$56.19万
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财政年份:2018
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Neuronal Orchestration of Metabolic State and Longevity
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批准号:10372000
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资助金额:$56.19万
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财政年份:2018
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G Protein-Mediated Integration of Oxygen Sensing and Energy Balance in C. Elegans
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批准号:8817284
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项目类别:
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资助金额:$41.22万
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财政年份:2013
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负责人:Supriya Srinivasan
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依托单位:
G Protein-Mediated Integration of Oxygen Sensing and Energy Balance in C. Elegans
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批准号:8634771
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项目类别:
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资助金额:$41.22万
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财政年份:2013
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负责人:Supriya Srinivasan
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依托单位:
G Protein-Mediated Integration of Oxygen Sensing and Energy Balance in C. Elegans
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批准号:9020225
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项目类别:
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资助金额:$41.87万
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财政年份:2013
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负责人:Supriya Srinivasan
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依托单位:
G Protein-Mediated Integration of Oxygen Sensing and Energy Balance in C. Elegans
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批准号:8543906
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项目类别:
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资助金额:$21.93万
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财政年份:2012
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负责人:Supriya Srinivasan
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依托单位:
The Role of Serotonin in Energy Homeostasis in C. elegans
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批准号:7324818
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项目类别:
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资助金额:$9.0万
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财政年份:2007
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负责人:Supriya Srinivasan
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依托单位:
The Role of Serotonin in Energy Homeostasis in C. elegans
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批准号:7885003
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项目类别:
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资助金额:$24.9万
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财政年份:2007
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负责人:Supriya Srinivasan
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依托单位:
The Role of Serotonin in Energy Homeostasis in C. elegans
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批准号:7223604
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项目类别:
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资助金额:$9.0万
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财政年份:2007
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负责人:Supriya Srinivasan
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依托单位:
The Role of Serotonin in Energy Homeostasis in C. elegans
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批准号:7924881
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项目类别:
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资助金额:$24.9万
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财政年份:2007
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负责人:Supriya Srinivasan
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依托单位:
The Role of Serotonin in Energy Homeostasis in C. elegans
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批准号:8133385
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项目类别:
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资助金额:$24.65万
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财政年份:2007
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负责人:Supriya Srinivasan
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依托单位:
海外基金