A Human-Specific Gene (G72/G30) in Transgenic Mice
A Human-Specific Gene (G72/G30) in Transgenic Mice
批准号:
7492569
负责人:
Chunyu Liu
金额:
$15.02万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-05-01 至 2010-04-30
关键词:
AllelesAmino Acid SequenceAsiansBacterial Artificial ChromosomesBacterial ChromosomesBehavioralBehavioral GeneticsBiochemicalBiologicalBiologyBipolar DisorderBrainBrain regionCharacteristicsChinese PeopleChromosomesCloningComplexD-Amino Acid DehydrogenaseDNADNA copy numberDataDevelopmentDiseaseDisease AssociationFamilyGene ExpressionGenerationsGenesGeneticGenetic PolymorphismGenetic RecombinationGenotypeHumanIndividualKnowledgeLeadLocationMeasurementMeasuresMental disordersMeta-AnalysisMethodsMitochondriaMusN-Methyl-D-Aspartate ReceptorsNational Institute of Mental HealthNeurobiologyOrthologous GeneOutcomePathway interactionsPatientsPeptide Sequence DeterminationPhasePhase I Clinical TrialsPolymerase Chain ReactionPredispositionPrimatesProceduresProteinsPsyche structureRegulationReverse TranscriptionRiskRoleSchizophreniaSerineSingle Nucleotide PolymorphismSpecificitySucroseSwimmingTestingTimeTranscriptTransgenic MiceVariantWaterWestern BlottingWild Type Mousebehavior testenzyme activityfunctional genomicsimprovedin vivointerestmouse genomepreferenceprepulse inhibitionreceptor bindingresearch study
中文摘要
描述(由申请人提供):G72/G30是染色体13q33.2上的一个正反义基因复合体,也被称为DAOA (d -氨基酸氧化酶激活剂),在多项研究中与精神分裂症和双相情感障碍有关。G72/G30的疾病关联及其作为少数灵长类特异性基因之一的特点使其成为人类大脑和精神疾病生物学研究中一个非常有趣的靶点。我们最近对精神分裂症的荟萃分析表明,G72/G30中的两个snp在亚洲人中显示出基因范围内的显著关联。在这个应用程序中,我们建议筛选亚洲精神分裂症患者(dna已由NIMH遗传学倡议收集),以寻找携带与精神分裂症相关的等位基因的个体。然后,我们将使用转化相关重组(TAR)克隆方法从选定的精神分裂症患者中分离G72细菌人工染色体(BAC)克隆。分离的克隆将被引入小鼠基因组,以产生转基因小鼠系。然后,我们将对三种类型的小鼠进行生化,基因表达和行为测试:本研究中生产的新转基因小鼠系,我们现有的携带无风险等位基因的G72转基因小鼠系,以及野生型小鼠。遗传学、功能基因组学和行为遗传学方法的综合应用将使我们更好地了解G72在脑功能和精神分裂症易感性中的生物学作用。我们将创建一个转基因小鼠系,它携带人类G72/G30基因复合体和精神分裂症风险等位基因。G72(我们称之为复合物)是与双相情感障碍和精神分裂症最一致的相关基因之一。由于G72是灵长类特有的基因,在人类中表达水平较低,因此对G72在人类中的生物学研究尤其具有挑战性。利用本次申请生成的新的转基因小鼠,以及我们现有的不含精神分裂症风险等位基因的G72转基因小鼠,我们可以对G72进行生物和行为功能的体内测试。我们期望这些结果将最终使我们更好地了解G72及其在正常人脑功能和精神疾病状态中的作用。
英文摘要
DESCRIPTION (provided by applicant): G72/G30, a sense-antisense gene complex on chromosome 13q33.2 also known as DAOA (D-amino acid oxidase activator), has been associated with schizophrenia and bipolar disorder in multiple studies. The disease association and its characteristic of being one of the very few primate-specific genes make G72/G30 a very intriguing target in the biological study of human brain and mental diseases. Our most recent meta-analysis of schizophrenia indicates that two SNPs in G72/G30 show gene-wide significant association in Asians. In this application, we propose to screen Asian schizophrenia patients (DNAs have been collected by the NIMH Genetics Initiative) for an individual carrying the allele that shows association with schizophrenia. Then, we will use the Transformation Associated Recombination (TAR) Cloning method to isolate G72 Bacterial Artificial Chromosome (BAC) clones from the selected schizophrenia patient. The isolated clone will be introduced into a mouse genome to produce a transgenic mouse line. We will then perform biochemical, gene expression, and behavioral tests on three types of mice: the new transgenic mouse line produced in this study, our existing G72 transgenic mouse line that carries the non-risk allele, and wild type mice. Comprehensive use of genetic, functional genomics and behavioral genetics approaches should lead us to an improved understanding of the biology of G72 in brain function and in schizophrenia susceptibility. We will create a transgenic mouse line that carries a human G72/G30 gene complex with a schizophrenia risk allele. G72 (as we refer to the complex) is one of the most consistently associated genes with both bipolar disorder and schizophrenia. Because G72 is a primate-specific gene with low expression levels in human, biological study of G72 in humans is particularly challenging. With the new transgenic mouse generated in this application, and our existing G72 transgenic mouse without the schizophrenia risk allele, we can perform in vivo tests on G72 biological and behavioral functions. We expect these results will ultimately lead to a better understanding of G72 and its role in both normal human brain function and psychiatric disease states.
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会议论文
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海外基金