Roles of Histone H3K27 demethylases in germ cell epigenetic development
组蛋白 H3K27 去甲基酶在生殖细胞表观遗传发育中的作用
基本信息
- 批准号:7807948
- 负责人:
- 金额:$ 5.22万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2009
- 资助国家:美国
- 起止时间:2009-04-01 至 2011-03-31
- 项目状态:已结题
- 来源:
- 关键词:AdultAllelesAnimal ModelBindingBiological AssayBiological ModelsCaenorhabditis elegansCell AgingCell Differentiation processCell LineageCell MaintenanceCell ProliferationCell divisionCellsCellular biologyComplexDataDefectDevelopmentDevelopmental BiologyDiseaseES Cell LineEmbryoEmbryonic DevelopmentEpigenetic ProcessEventGene ActivationGene ExpressionGene SilencingGenesGenetic ModelsGenomicsGerm CellsGonadal structureHistonesLightLysineMaintenanceMalignant NeoplasmsMalignant neoplasm of prostateMethylationModificationMusMutagenesisMutant Strains MiceMutationNatureNucleosomesOncogenicOrganogenesisPathway interactionsPhasePhenotypePlayPolycombPost-Translational Protein ProcessingRegulationRegulator GenesRepressionRett SyndromeRoleSpermatogenesisStagingStem cellsStructureStructure of primordial sex cellTestingTestisTransferaseX InactivationZebrafishchromatin immunoprecipitationchromatin modificationdemethylationderepressiongastrulationgene repressionhuman diseaseimprintin vivomigrationmouse modeloverexpressionpluripotencypromoterstem cell differentiationtumorigenesisvector
项目摘要
DESCRIPTION (provided by applicant): Histone posttranslational modifications regulate nucleosome structure and thus gene expression. Histone H3 Lysine 27 (H3K27) methylation is a global regulator of gene activation/repression and contributes to the epigenetic inheritance of defined transcriptional states across cell divisions. The establishment of a mature germline is characterized by several well-defined epigenetic changes throughout embryonic and adult germ cell development. I plan to study the role of Histone H3K27 demethylases in major events of germ cell developmental biology. I hypothesize that Utx and JmjdS H3K27 demethylases are required in the early mammalian embryo and will prove essential for reprogramming and differentiation events that are critical for development of mature gametes. To test this hypothesis, my proposal will utilize mouse genetic models to assess the global and cell specific impact of H3K27 demethylases in germ cell biology. While these studies focus on germ cell development, my findings will bring to light in vivo function of Utx and JmjdS in H3K27 demethylation, how these demethylases operate in mammalian organismal development, and how they regulate stem cell differentiation/pluripotency within the germ cell lineage. Epigenetics plays a major role in human disease, specifically in the form of imprinted and epigenetic gene disorders (such as Beckwith-Widemann, Prader-Willi, Angelmann, and Rett syndromes) or globally in large scale epigenetic changes of cancer. Overexpression of H3K27 methyl-transferases regulates cellular proliferation in prostate cancer, while loss of H3K27 trimethylation is associated with cellular senescence. Understanding how H3K27 demethylases regulate cell fate decisions within the germ cell lineage may be amendable to understanding the oncogenic nature of misregulated cellular differentiation events in cancer. The potential therapeautic implications of H3K27 demethylases towards these ends are limitless, but we must first have a basic understanding of how they regulate cellular fate decisions.
描述(由申请人提供):组蛋白翻译后修饰调节核小体结构,从而调节基因表达。组蛋白 H3 赖氨酸 27 (H3K27) 甲基化是基因激活/抑制的全局调节因子,有助于跨细胞分裂的特定转录状态的表观遗传。成熟种系的建立的特点是整个胚胎和成体生殖细胞发育过程中的几个明确的表观遗传变化。我计划研究组蛋白 H3K27 去甲基酶在生殖细胞发育生物学重大事件中的作用。我假设 Utx 和 JmjdS H3K27 去甲基酶是早期哺乳动物胚胎所必需的,并且将证明对于成熟配子发育至关重要的重编程和分化事件至关重要。为了验证这一假设,我的建议将利用小鼠遗传模型来评估 H3K27 去甲基酶在生殖细胞生物学中的整体和细胞特异性影响。虽然这些研究重点关注生殖细胞发育,但我的研究结果将揭示 Utx 和 JmjdS 在 H3K27 去甲基化中的体内功能、这些去甲基化酶如何在哺乳动物有机体发育中发挥作用,以及它们如何调节生殖细胞谱系内的干细胞分化/多能性。表观遗传学在人类疾病中发挥着重要作用,特别是在印记和表观遗传基因疾病(例如 Beckwith-Widemann、Prader-Willi、Angelmann 和 Rett 综合征)或全球癌症的大规模表观遗传变化中。 H3K27 甲基转移酶的过度表达可调节前列腺癌中的细胞增殖,而 H3K27 三甲基化的丧失与细胞衰老相关。了解 H3K27 去甲基酶如何调节生殖细胞谱系内的细胞命运决定可能有助于了解癌症中失调的细胞分化事件的致癌性质。 H3K27 去甲基酶对这些目的的潜在治疗意义是无限的,但我们必须首先对它们如何调节细胞命运决定有一个基本的了解。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
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Karl Bryan Shpargel其他文献
Karl Bryan Shpargel的其他文献
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{{ truncateString('Karl Bryan Shpargel', 18)}}的其他基金
Enhancer activation mechanisms in cranial neural crest osteoblast differentiation
颅神经嵴成骨细胞分化的增强子激活机制
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10475308 - 财政年份:2021
- 资助金额:
$ 5.22万 - 项目类别:
Enhancer activation mechanisms in cranial neural crest osteoblast differentiation
颅神经嵴成骨细胞分化的增强子激活机制
- 批准号:
10663985 - 财政年份:2021
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Enhancer activation mechanisms in cranial neural crest osteoblast differentiation
颅神经嵴成骨细胞分化的增强子激活机制
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Enhancer activation roles and mechanisms in craniofacial development
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10214979 - 财政年份:2020
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Epigenetic mechanism of histone modifying enzymes in craniofacial development
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$ 5.22万 - 项目类别:
Roles of Histone H3K27 demethylases in germ cell epigenetic development
组蛋白 H3K27 去甲基酶在生殖细胞表观遗传发育中的作用
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7674206 - 财政年份:2009
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