Molecular Pathways Controlling Ovarian Gene Expression
Molecular Pathways Controlling Ovarian Gene Expression
批准号:
7761207
负责人:
CARLOS OSCAR STOCCO
金额:
$30.08万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-02-01 至 2014-01-31
关键词:
AchievementActivinsAddressAdenovirusesAllelesAndrogensAnimalsApoptosisApoptoticAromataseBiological AssayCYP17A1 geneCell Culture TechniquesCell Cycle ProgressionCell DeathCell ProliferationCell physiologyCellsCodeDNADefectDevelopmentEmbryoEnzymesEstradiolEstrogensEtiologyFemaleFertilityGene ExpressionGene Expression RegulationGene TargetingGenesGenetic RecombinationGenomicsGranulosa-Lutein CellsGrowthHormonesIn VitroInfectionInfertilityInvestigationKnockout MiceKnowledgeLightMicroarray AnalysisMolecularMusOvarianOvarian CyclesOvarian DiseasesOvarian Granulosa CellOvaryPaperPathway interactionsPhysiologicalPlayProductionPublishingReproductive ProcessRoleStagingSterile coveringsSteroid biosynthesisSteroidsStructureTechnologyTestingdesignfolliculogenesisgene repressiongranulosa cellgranulosa cell tumorimproved functioningin vivomutantoverexpressionpublic health relevancerecombinaseresponsetheca celltranscription factor
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Coordinated activation and repression of genes are essential for the normal progress of the ovarian cycle. Ovarian granulosa cells express high levels of the transcription factors GATA-4 and GATA-6. In cell cultures, these transcription factors were shown to play key roles in the expression of enzymes involved in steroidogenesis. We have demonstrated in several recently published papers that GATA-4 is critical for the production of estradiol, which is essential for granulosa cell proliferation and follicle maturation. In addition, the finding that low expression of GATA-4 is associated with follicular cell death suggests that this factor also plays a survival role in the ovary. Because GATA-4 and GATA-6 null mice are embryonic lethal, the ultimate role of GATA in ovarian function remains unknown. This study is therefore designed to determine the physiological role of GATA-4 and GATA-6 in ovarian steroidogenesis, follicular development, and female fertility. The specific aims of this study are: 1- To generate ovarian-specific GATA-4 and GATA-6 null mice in order to find out the explicit roles of these transcription factors in the ovary in vivo. The Cre-lox technology will be used to delete part of the coding region of GATA-4, GATA-6, or their combination. We expect these mice to have severe defects in steroid production and in follicular development. 2- To determine the effect of GATA-4 and GATA-6 deletion on ovarian cells in vitro. Granulosa cells lacking GATA-4, GATA-6, or both will be used to examine the specific roles of these factors in steroidogenesis, cell proliferation, granulosa-cell hormone response, and gene expression. 3- To identify those genes that are regulated by GATA-4 and GATA-6 in fully functional ovaries in vivo, we will use ChIP-on-chip assays. All the results obtained to date indicate that GATA-4 and GATA-6 may play a crucial role in the normal function of the ovary. We expect from this investigation to clearly define the function of GATA-4 and GATA-6 in the steroidogenic capacity and growth of granulosa cells, to determine whether GATA-4 and GATA-6 have redundant effects on these cells, and to identify GATA-4 and GATA-6 target genes in the ovary. This study will not only provide critically important information on the regulatory mechanism underlying normal ovarian function but also may shed light on ovarian diseases due to improper granulosa cell function such as granulosa cell tumors and infertility. PUBLIC HEALTH RELEVANCE: The roles of the transcription factors GATA-4 and GATA-6 in folliculogenesis and fertility will be addressed. These studies will contribute to better understanding of the cellular and molecular mechanisms that control ovarian function and improve our knowledge of the etiology of ovarian diseases such as granulosa cell tumors and infertility.
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会议论文
Salt-Inducible Kinase Regulation of Ovarian Granulosa Cells
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批准号:10011939
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项目类别:
-
资助金额:$33.9万
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财政年份:2019
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负责人:CARLOS OSCAR STOCCO
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依托单位:
Salt-Inducible Kinase Regulation of Ovarian Granulosa Cells
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批准号:10165768
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项目类别:
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资助金额:$33.23万
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财政年份:2019
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负责人:CARLOS OSCAR STOCCO
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依托单位:
Salt-Inducible Kinase Regulation of Ovarian Granulosa Cells
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批准号:10406988
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项目类别:
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资助金额:$33.23万
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财政年份:2019
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负责人:CARLOS OSCAR STOCCO
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依托单位:
Salt-Inducible Kinase Regulation of Ovarian Granulosa Cells
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批准号:10643707
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项目类别:
-
资助金额:$33.23万
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财政年份:2019
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负责人:CARLOS OSCAR STOCCO
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依托单位:
Regulation of Aromatase Expression in the Corpus Luteum
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批准号:8045278
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项目类别:
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资助金额:$19.63万
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财政年份:2011
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负责人:CARLOS OSCAR STOCCO
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依托单位:
Regulation of Aromatase Expression in the Corpus Luteum
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批准号:8206281
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项目类别:
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资助金额:$19.63万
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财政年份:2011
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负责人:CARLOS OSCAR STOCCO
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依托单位:
Molecular Pathways Controlling Ovarian Gene Expression
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批准号:8044047
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项目类别:
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资助金额:$28.87万
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财政年份:2009
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负责人:CARLOS OSCAR STOCCO
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依托单位:
Molecular Pathways Controlling Ovarian Gene Expression
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批准号:8431437
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项目类别:
-
资助金额:$27.4万
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财政年份:2009
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负责人:CARLOS OSCAR STOCCO
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依托单位:
Molecular Pathways Controlling Ovarian Gene Expression
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批准号:7913605
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项目类别:
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资助金额:$22.53万
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财政年份:2009
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负责人:CARLOS OSCAR STOCCO
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依托单位:
Molecular Pathways Controlling Ovarian Gene Expression
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批准号:8212331
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项目类别:
-
资助金额:$28.87万
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财政年份:2009
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负责人:CARLOS OSCAR STOCCO
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依托单位:
Estradiol Production by Prostaglandin F2alpha
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批准号:7020725
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项目类别:
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资助金额:$7.98万
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财政年份:2005
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负责人:CARLOS OSCAR STOCCO
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依托单位:
Estradiol Production by Prostaglandin F2alpha
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批准号:6921159
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项目类别:
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资助金额:$8.18万
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财政年份:2005
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负责人:CARLOS OSCAR STOCCO
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依托单位:
海外基金