Genetic analysis of Htr2c RNA editing in amygdala
Genetic analysis of Htr2c RNA editing in amygdala
批准号:
7257336
负责人:
DAVID C AIREY
金额:
$23.89万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-05-15 至 2009-04-30
关键词:
5-HydroxytryptophanAffectAllelesAmygdaloid structureAnxietyAnxiety DisordersBehaviorBehavioralBiological MarkersBrainBrain regionBreedingCodeCollaborationsComplex Genetic TraitComputer SimulationDataDevelopmentDoctor of PhilosophyEmotionalEnd PointEnsureEquilibriumFrightGene ExpressionGene Expression ProfileGenesGeneticGenetic MarkersGenetic Predisposition to DiseaseGenetic screening methodGenomeGenome ScanGoalsGrantHumanHydroxyindoleacetic AcidInbred StrainInbred Strains MiceInvestigationJointsLaboratoriesLearningLigandsMapsMeasurementMeasuresMemoryMental DepressionMental HealthMental disordersMetabolismMethodsMusNucleotidesOther GeneticsPaperPhenotypePlayPropertyProtein IsoformsPublishingQuantitative Trait LociRNARNA EditingRandomizedRecombinantsRegulationResearchRoleSerotoninSerotonin Receptor 5-HT2CSignal TransductionSiteSourceStressSurveysSynapsesTestingTryptophan 5-monooxygenaseVariantbasecongenicendophenotypegenetic analysisreceptorserotonin transportertraitvirtual
中文摘要
描述(由申请人提供):Htr 2c RNA编辑通过产生多达24种具有不同信号转导特性的受体亚型,改变5-HT 2C受体对脑功能的潜在贡献。 Htr 2c RNA编辑是肾上腺素能功能和精神疾病的重要内表型,了解这种变异的遗传病因是一个重要目标。 药理学操作暗示同源配体5-羟色胺(5-HT)参与RNA编辑的5-HT 2C受体的调节。 近交系小鼠在血清素和RNA编辑方面的差异暗示了变异的遗传来源。 已知两种单核苷酸多态性影响小鼠的多巴胺能功能。 目的1、2和3利用40个BXD重组近交系小鼠的平衡析因表,其代表SNP Tph 2:Pro447 Arg和Slc 6a 4:Glu 39 Gly的每种双等位基因组合。 因为BXD RI系的遗传背景已经通过育种随机化,所以这组小鼠本质上表现为色氨酸羟化酶和5-羟色胺转运蛋白基因中两个重要功能SNP的虚拟双同源。 目的1测试这些SNP作为影响Htr 2c RNA编辑谱的数量性状核苷酸(QTN)的候选性。 目的2使用全基因组QTL定位来更广泛地探索可能影响Htr 2c RNA编辑谱的其他遗传位点。 目的3探索Htr 2c RNA编辑的行为和转录组相关性。 研究的小鼠大脑区域是杏仁核,其富含5-HT 2C受体,并在压力、焦虑、恐惧和情绪学习和记忆中起重要作用。 在人类中,杏仁核似乎在相关的心理障碍中发挥作用。 血清素2C受体是心理健康研究的焦点。 该提案旨在发现RNA变异的遗传原因和行为相关性,该RNA编码血清素2C受体的多达24种功能不同的蛋白质亚型。 研究的大脑区域是杏仁核,它富含5-羟色胺2C受体,在焦虑症和抑郁症中起着重要作用。
英文摘要
DESCRIPTION (provided by applicant): Htr2c RNA editing alters the potential contribution of 5-HT2C receptors to brain function by producing up to 24 receptor isoforms with different signal transduction properties. Htr2c RNA editing is an important endophenotype for serotonergic function and psychiatric disease, and understanding the genetic etiology of this variation is an important goal. Pharmacological manipulations implicate the cognate ligand serotonin (5-HT) in the regulation of RNA edited 5-HT2C receptors. Inbred mouse strain differences in both serotonin and RNA editing implicate genetic sources of variation. Two single nucleotide polymoprhisms are known to affect serotonergic function in mice. Aims 1, 2, and 3 make use of a balanced factorial table of 40 BXD recombinant inbred lines of mice that represent every two-allele combination of the SNPs Tph2:Pro447Arg and Slc6a4:Glu39Gly. Because the genetic background of the BXD RI lines has been randomized by breeding, this panel of mice in essence performs as a virtual double congenic for two important functional SNPs in the genes for tryptophan hydroxylase and the serotonin transporter. Aim 1 tests the candidacy of these SNPs as quantitative trait nucleotides (QTNs) affecting Htr2c RNA editing profiles. Aim 2 uses genome-wide QTL mapping to explore more broadly other genetic loci that may influence Htr2c RNA editing profiles. Aim 3 proposes to explore behavioral and transcriptome correlates of Htr2c RNA editing. The mouse brain region of investigation is the amygdala, which is rich in 5-HT2C receptors and plays important functional roles in stress, anxiety, fear, and emotional learning and memory. In humans, the amygdala appears to function in related psychological disorders. The serotonin 2C receptor is a focus of mental health research. This proposal aims to discover genetic causes and behavioral correlates of variation in RNA that codes for up to 24 functionally different protein isoforms of the serotonin 2C receptor. The brain region of investigation is the amygdala, which is rich in serotonin 2C receptors and plays important roles in anxiety disorders and depression.
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Genetic analysis of Htr2c RNA editing in amygdala
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批准号:7424075
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项目类别:
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资助金额:$13.66万
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财政年份:2007
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负责人:DAVID C AIREY
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依托单位:
Serotonergic regulation of sensorimotor gating in mice
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批准号:6690887
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项目类别:
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资助金额:$4.99万
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财政年份:2003
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负责人:DAVID C AIREY
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依托单位:
CONTROL OF MOUSE RETINAL CELL POPULATIONS: RODS & CONES
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批准号:6135044
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项目类别:
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资助金额:$3.09万
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财政年份:2000
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负责人:DAVID C AIREY
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依托单位:
海外基金