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Biochemical Studies of a Transcription Factor

Biochemical Studies of a Transcription Factor
转录因子的生化研究
批准号:
8004618
负责人:
MICHAEL Aaron WEISS
金额:
$9.91万
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-01-08 至 2010-12-31
关键词:
AbbreviationsAddressAdmixtureAdultAllelesAnimalsBehaviorBehavioralBehavioral GeneticsBindingBiochemicalBiochemistryBiologicalBiological ProcessC-terminalCaenorhabditis elegansChromosomes, Human, Pair 9Co-ImmunoprecipitationsCollaborationsComplement component C1sComplexCongenital AbnormalityCoupledCourtshipDNADNA BindingDNA Sequencing FacilityDatabasesDevelopmentDevelopmental BiologyDimerizationDiseaseDrosophila genusDrosophila melanogasterElementsExhibitsFamilyFemaleFoundationsGene Expression RegulationGene TargetingGenesGeneticGenetic TranscriptionGoalsHandHomeobox GenesHumanHuman ChromosomesHybridsIn VitroIndiumInfertilityLaboratoriesLocationMass Spectrum AnalysisMeasurementMediatingMethodsModelingMolecularMolecular GeneticsMutationN-terminalNervous system structureNewborn InfantNuclear Magnetic ResonancePhenotypePropertyProtein BindingProtein IsoformsProteinsProteomicsProtonsRNA SplicingRegulationResearchResolutionScreening procedureSexual DevelopmentSignal TransductionSiteSpecific qualifier valueStagingStructureStructure-Activity RelationshipSyndromeSystemTailTechnologyTemperatureTissuesTranscription CoactivatorTranscription Factor 3TransgenesTransgenic OrganismsUbiquitinValidationVariantWorkYeastsbasedesigndimerflygel mobility shift assaygenetic analysisgonadal cancerin vivoinnovationinsightintercellular communicationloss of functionmalememberneural circuitnuclear Overhauser enhancementnull mutationprogramsprotein functionprotein protein interactionprotein structurepublic health relevancesexsex determinationsexual dimorphismstructural biologytraittranscription factoryeast two hybrid system

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DESCRIPTION (provided by applicant): Development in metazoans is regulated by specific regulatory hierarchies leading to the stage- and tissue-specific expression of transcriptional networks. Understanding such networks poses a major challenge in developmental biology. A model is provided by the regulation of sexual dimorphism in Drosophila melanogaster. This collaborative R01 application from the laboratories of M. Weiss (CWRU) and B. Baker (Stanford) focuses on Doublesex (DSX), a member of a newly recognized family of DM transcription factors broadly involved in metazoan development, including in humans. Our long-term goal is a molecular understanding of how information is transmitted from the primary determinants of sex to the genes responsible for the morphological, biochemical, and behavioral differences between the sexes. The doublesex (dsx) gene controls a major branch of the sex-determining hierarchy of D. melanogaster. The doublesex (dsx) gene encodes sex-specific protein isoforms (designated DSXF (female) and DSXM (male)) as a consequence of sex-specific RNA splicing. Although DSXF and DSXM have opposing biological functions, they exhibit similar DNA-binding properties and so presumably recognize the same cis- acting control elements in target genes. DSXF (but not DSXM) interacts with transcriptional coactivator Intersex (IX), presumably leading to assembly of a female-specific multiprotein-DNA complex at target genes. Such sex-specific regulatory properties presumably underlie the function of dsx as a prototypical "behavioral gene" in the nervous system: DSXM regulates sine singing, a component of the male courtship song, whereas DSXF is hypothesized to regulate major features of female courtship behavior, including rejection behavior. We seek to investigate the molecular bases of the sex-specific functions of DSXF and DSXM with application to behavioral genetics. To these ends, an innovative interdisciplinary strategy is proposed that integrates molecular genetics with biochemistry, proteomics, and structural biology. Studies will focus on the respective C-terminal domains of DSXF/M containing sex-specific tails. In addition, newly described methods for gene targeting in vivo will be employed to investigate the relationship between dsx as a behavioral gene and a discrete and quantifiable repertoire of behavioral elements. Because deletions of DSX-related genes in human chromosome 9 are associated with intersexual abnormalities of the newborn, our results may also provide insight into a major class of human birth defects. Public Health Relevance: How the differences between male and female animals are specified by genes defines a major scientific problem. We are studying sex-specific genes in fruit flies to gain insight into human birth defects, infertility syndromes, and cancers of the gonads.
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How Insulin Binds to the Insulin Receptor
  • 批准号:
    8003136
  • 项目类别:
  • 资助金额:
    $4.43万
  • 财政年份:
    2010
  • 负责人:
    MICHAEL Aaron WEISS
  • 依托单位:
Design of an Implantable Pump Insulin
  • 批准号:
    8003137
  • 项目类别:
  • 资助金额:
    $5.69万
  • 财政年份:
    2010
  • 负责人:
    MICHAEL Aaron WEISS
  • 依托单位:
Clinical Testing of an Insulin Analog
  • 批准号:
    7613905
  • 项目类别:
  • 资助金额:
    $25.5万
  • 财政年份:
    2009
  • 负责人:
    MICHAEL Aaron WEISS
  • 依托单位:
Design of an Implantable Pump Insulin
  • 批准号:
    7795721
  • 项目类别:
  • 资助金额:
    $31.09万
  • 财政年份:
    2008
  • 负责人:
    MICHAEL Aaron WEISS
  • 依托单位:
海外基金