A Human-Specific Gene (G72/G30) in Transgenic Mice
A Human-Specific Gene (G72/G30) in Transgenic Mice
批准号:
8051049
负责人:
Elliot S Gershon
金额:
$20.61万
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 2012-04-30
关键词:
AllelesAmino Acid SequenceAsiansBacterial Artificial 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 DeterminationPhasePredispositionPrimatesProceduresProteinsPsyche structureRegulationReverse TranscriptionRiskRoleSchizophreniaSerineSingle Nucleotide PolymorphismSpecificitySucroseSwimmingTestingTimeTranscriptTransgenic MiceVariantWaterWestern BlottingWild Type Mousebehavior testenzyme activityfunctional genomicsimprovedin vivointerestmouse genomephase 1 studypreferenceprepulse inhibitionreceptor bindingresearch study
中文摘要
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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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科研奖励(0)
会议论文
2/5 Biomarkers/Biotypes, Course of Early Psychosis and Specialty Services (BICEPS)
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批准号:10681376
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资助金额:$27.56万
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财政年份:2022
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负责人:Elliot S Gershon
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2/5-Clozapine Response and Biomarker Correlates in Low-IEA Biotype-1
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批准号:10397395
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资助金额:$36.45万
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财政年份:2021
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2/5-Clozapine Response and Biomarker Correlates in Low-IEA Biotype-1
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批准号:10613447
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资助金额:$36.45万
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财政年份:2021
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依托单位:
2/5 Bipolar-Schizophrenia Network for Intermediate Phenotypes 2 (B-SNIP2) - Diversity Supplement
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批准号:9464262
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资助金额:$4.78万
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财政年份:2017
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依托单位:
2/5 Bipolar-Schizophrenia Network for Intermediate Phenotypes 2 (B-SNIP2)
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批准号:9293383
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项目类别:
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资助金额:$79.36万
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财政年份:2015
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负责人:Elliot S Gershon
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依托单位:
Multidisciplinary Psychiatry Genetics Training Program
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批准号:8116495
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资助金额:$6.68万
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财政年份:2002
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负责人:Elliot S Gershon
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依托单位:
Fine Genomic Mapping of 13q32 in Bipolar Disorder
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批准号:6612911
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资助金额:$61.18万
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财政年份:2002
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负责人:Elliot S Gershon
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依托单位:
Multidiciplinary Psychiatric Genetics Training Program
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批准号:7113813
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项目类别:
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资助金额:$10.57万
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财政年份:2002
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负责人:Elliot S Gershon
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依托单位:
Multidisciplinary Psychiatry Genetics Training Program
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批准号:7908911
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项目类别:
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资助金额:$12.9万
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财政年份:2002
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负责人:Elliot S Gershon
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依托单位:
Multidisciplinary Psychiatry Genetics Training Program
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批准号:7467283
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项目类别:
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资助金额:$8.89万
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财政年份:2002
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负责人:Elliot S Gershon
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依托单位:
Fine Genomic Mapping of 13q32 in Bipolar Disorder
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批准号:6463293
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资助金额:$55.86万
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财政年份:2002
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负责人:Elliot S Gershon
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依托单位:
Fine Genomic Mapping of 13q32 in Bipolar Disorder
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财政年份:2002
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依托单位:
Fine Genomic Mapping of 13q32 in Bipolar Disorder
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批准号:7085396
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资助金额:$60.43万
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财政年份:2002
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负责人:Elliot S Gershon
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依托单位:
Multidiciplinary Psychiatric Genetics Training Program
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批准号:6734172
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项目类别:
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资助金额:$9.27万
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财政年份:2002
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依托单位:
Multidisciplinary Psychiatry Genetics Training Program
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批准号:7660454
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资助金额:$11.49万
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财政年份:2002
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负责人:Elliot S Gershon
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依托单位:
Multidiciplinary Psychiatric Genetics Training Program
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项目类别:
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资助金额:$10.68万
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财政年份:2002
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依托单位:
Multidiciplinary Psychiatric Genetics Training Program
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批准号:6612854
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资助金额:$11.1万
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财政年份:2002
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负责人:Elliot S Gershon
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依托单位:
Fine Genomic Mapping of 13q32 in Bipolar Disorder
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批准号:6908242
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资助金额:$62.7万
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依托单位:
Multidiciplinary Psychiatric Genetics Training Program
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批准号:6898712
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项目类别:
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资助金额:$10.06万
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负责人:Elliot S Gershon
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依托单位:
Genetic Linkage Studies in Bipolar Disorder Families
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资助金额:$37.45万
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财政年份:2000
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负责人:Elliot S Gershon
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依托单位:
海外基金