Cross-Species Investigation of Gene Networks for Ethanol-Related Behaviors
Cross-Species Investigation of Gene Networks for Ethanol-Related Behaviors
批准号:
8904558
负责人:
KENNETH SEEDMAN KENDLER
金额:
$136.83万
依托单位国家:
美国
项目类别:
财政年份:
2014
资助国家:
美国
项目状态:
已结题
起止时间:
2014-08-05 至 2019-05-31
关键词:
AcuteAddressAffectAlcoholsAnimal ModelBehavioralBehavioral GeneticsBioinformaticsCaenorhabditis elegansCandidate Disease GeneChronicClinicalCommunitiesControlled EnvironmentDataDevelopmentDiagnosticDrosophila genusEnvironmentEthanolEtiologyFundingFutureGene Expression RegulationGenesGeneticGenetic VariationGenetic studyGenomeGenomicsGenotypeGoalsGrantHealthHumanHuman GeneticsHuman GenomeIndividualInformaticsInvertebratesInvestigationJointsLaboratoriesLettersMediatingMeta-AnalysisModelingMolecularMolecular ProfilingMusNational Institute on Alcohol Abuse and AlcoholismPhenotypePositioning AttributePredispositionPreventionPublic HealthRattusResearch PersonnelResearch Project GrantsResourcesRewardsRiskRodentRoleSignal TransductionStructureSubstance abuse problemSumSyndromeSystemSystems BiologyTNFRSF5 geneTestingTherapeuticValidationVariantWorkalcohol behavioralcohol researchalcohol responsealcohol sensitivityalcohol use disorderbehavioral responsedata sharingdesignflygene discoverygenetic analysisgenetic approachgenetic risk factorgenetic variantgenome wide association studyimprovedinterestnew therapeutic targetnext generation sequencingnovelprogramsrisk varianttherapeutic developmenttoolvalidation studies
中文摘要
描述(由申请人提供):酒精使用障碍(AUD)是一个主要的公共卫生负担。遗传风险因素对AUDs的易感性起着关键作用,可能是许多变异的结果,每种变异都对风险有一定的影响。迄今为止,动物模型和人类的遗传学研究在识别基因个体风险变体方面进展缓慢。然而,现代高通量方法,如全基因组关联研究或基因组表达谱分析,有望快速增加影响AUDs的潜在候选基因库。这个P50酒精研究中心的建议提出了一个新颖的和高度集成的整体设计,专注于基因发现和AUDs遗传学的功能解释。该应用程序是P20发展中心资助的产物,该中心于2009年建立了VCU酒精研究中心。在取得重大进展之后,我们在此提议扩大该中心。我们的方法包括三个新的特点:1)关注与AUD相关的表型的基因网络,而不是单个基因; 2)跨物种遗传和基因组学分析,以验证影响乙醇行为的候选基因和网络; 3)高度集成的中心设计,通过跨项目的跨平台快速共享数据,物种分析管道,以提供排名的基因列表或网络,用于组件项目中的进一步实验验证。我们请求为六个研究项目提供五年的支持,并为小鼠、蠕虫、苍蝇和人类的遗传研究提供试点赠款。三个项目将在人类遗传学与一个新的临床实验室组成部分,用于评估有针对性的遗传对人类行为的影响,乙醇在受控环境中的反应。所有项目将由一个行政核心,一个分析和信息学核心和啮齿动物行为核心的支持。由于VCU-ARC组件的高度互动结构,这些项目和核心中提出的科学工作显然大于其部分的总和。VCU-ARC很有可能成为一个国家资源,为我们对AUDs病因及其预防和治疗的理解做出重大贡献。
英文摘要
DESCRIPTION (provided by applicant): Alcohol use disorders (AUDs) represent a major public health burden. Genetic risk factors contribute critically to susceptibility to AUDs likely a result of many variants each contributing modestly to risk. Genetic studies in animal models and humans have to date made slow progress in identifying genes individual risk variants. However, modern high-throughput approaches such as genome-wide association studies or genomic expression profiling promise to rapidly increase the pool of potential candidate genes influencing AUDs. This proposal for a P50 Alcohol Research Center presents a novel and highly integrated overall design to focus on both gene discovery and functional interpretation for the genetics of AUDs. This application is the outgrowth of a P20 Developmental Center grant that established the VCU Alcohol Research Center in 2009. Having made significant progress, we propose here to extend and enlarge that Center. Our approach includes three novel features: 1) A focus on gene networks contributing to AUD-related phenotypes, rather than single genes; 2) A cross-species genetic and genomics analysis to validate candidate genes and networks affecting ethanol behaviors; 3) A highly integrative Center design with rapid data sharing across projects through a cross-species analysis pipeline to provide ranked gene lists or networks for further experimental validation in the component projects. We request five years of support for six research projects and pilot grants for genetic studies in mice, worms, flies, and humans. Three projects will be in human genetics with a novel clinical laboratory component for assessing targeted genetic influences on human behavioral responses to ethanol in a controlled environment. All projects will be supported by an Administrative Core, an Analytic and Informatics Core and a Rodent Behavioral Core. The scientific work proposed in these projects and cores are clearly greater than the sum of their parts, due to the highly interactive structure of the VCU-ARC components. The VCU-ARC is well positioned to become a national resource making major contributions to the advancement of our understanding of the etiology of AUDs and their prevention and treatment.
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会议论文
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