Novel transcription factor for UCP-1 expression in brown fat
Novel transcription factor for UCP-1 expression in brown fat
批准号:
8070034
负责人:
Sarah M Paul
金额:
$4.68万
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:
2010-05-01 至 2012-01-31
关键词:
AdipocytesAdultAffectAffinity ChromatographyBindingBinding SitesBiochemicalBiological AssayBiologyBrown FatBurn injuryCell Differentiation processCellsComplexDNA BindingDNA SequenceDataDeletion MutationDevelopmentDiabetes MellitusDiseaseEpidemicFatty AcidsFatty acid glycerol estersFellowshipGelGelshift AnalysisGene ExpressionGenesGeneticGenetic TranscriptionGoalsHeart DiseasesHeatingIncidenceKnockout MiceLinkLongevityLuciferasesMass Spectrum AnalysisMediatingMetabolic DiseasesMetabolic syndromeMethodsMolecularMusMyoblastsNational Research Service AwardsNon-Insulin-Dependent Diabetes MellitusObesityOrganPrevalenceProcessPromoter RegionsProteinsRecruitment ActivityRegulationReporterResearch Project GrantsRoleScanningSeriesSocietiesTestingThermogenesisWorkZinc Fingerscell typeenergy balanceglobal healthin vivointerestloss of functionmembernoveloverexpressionpromoterprotein complexresearch studysmall hairpin RNAtranscription factoruncoupling protein 1
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Obesity is a global health epidemic that is associated with decreased life span and increased incidence of metabolic diseases like type 2 diabetes and heart disease. Two types of fat exist. White fat stores energy in the form of fatty acids, and brown fat is the mammalian thermogenic organ. Brown fat has recently proven to be present in adult humans-a finding which has drawn considerable interest because increases in brown fat- specific gene expression appear to protect again obesity and metabolic syndrome. While it is known that brown fat thermogenesis can tip the energy balance in favor of use rather than storage, how and why this occurs is unclear at the molecular level. Furthermore, anti-obesity strategies could include increasing expression of brown-fat specific thermogenic genes including uncoupling protein-1 (UCP1) as well as brown fat formation. Since not much is known about the brown fat transcriptional network, a better understanding of this fnetwork is the immediate goal for the research project. Our lab has identified a novel zinc finger transcription factor that is preferentially expressed in brown fat at a high level, and our preliminary data indicate one target of this transcription factor (designated as B2) is UCP1, the most important known thermogenic gene, which is found exclusively in brown fat and critical for brown fat thermogenesis. The goal of the work to be undertaken in this NRSA fellowship is to understand the biology of B2 and its role in brown fat. Aim 1 seeks to define the DNA binding site for B2 in the UCP1 promoter using biochemical and molecular approaches. Aim 2 is to identify the protein interaction partners of B2 by tandem affinity purification and mass spectrometry. Finally, Aim 3 is to assess the role of B2 in vivo by developing and analyzing B2 knockout mice. These studies will make an important contribution to the newly resurgent field of brown fat biology by characterizing the novel transcription factor B2 and may provide new directions for the study of brown fat in obesity.
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Novel transcription factor for UCP-1 expression in brown fat
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批准号:7911931
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项目类别:
-
资助金额:$5.67万
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财政年份:2010
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负责人:Sarah M Paul
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依托单位:
海外基金