Repression of the hTERT gene during cell differentiation

细胞分化过程中 hTERT 基因的抑制

• 批准号: 7654788
• 负责人: JIYUE ZHU
• 金额: $ 11.56万
• 依托单位: PENNSYLVANIA STATE UNIV HERSHEY MED CTR
• 依托单位国家: 美国
• 财政年份: 2004
• 资助国家: 美国
• 起止时间: 2004-08-01 至 2010-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7654788
• 关键词: Address; Adult; Architecture; Binding; Biological Assay; Cell Differentiation process; Cells; Chromatin; Chromatin Structure; Chromosomes; Complex; Data; Deoxyribonuclease I; Development; Elements; Environment; Event; Gene Expression Regulation; Genetic Transcription; Goals; Histones; Human; Hypersensitivity; Introns; Investigation; Maintenance; Maps; Measurement; Modeling; Modification; Molecular; Nuclear; Numbers; Plasmids; Play; Process; Promoter Regions; Rate; Regulation; Regulatory Element; Reporter; Repression; Resolution; Role; Site; Somatic Cell; Stem cells; Structure; System; TERT gene; Techniques; Telomerase; Transcriptional Regulation; Transgenic Organisms; U937 Cells; base; chromatin immunoprecipitation; chromatin remodeling; design; embryo tissue; gene repression; novel; promoter; transcription factor

DESCRIPTION (provided by applicant): Our long-term goal is to understand the critical steps of hTERT gene regulation during development. The hTERT gene, which encodes the rate-limiting subunit of human telomerase, is expressed at a high level in embryonic tissues and stem cells, but is repressed upon differentiation in the majority of adult somatic cells. Although the hTERT promoter has been studied extensively, the contribution of chromatin environment and the requirement of cis-elements have not been determined for the repression of the endogenous hTERT transcription. Previous results, including our own, have indicated that native chromatin plays a critical role in the regulation of hTERT transcription. hTERT transcription can be reversibly induced by inhibition of histone deacetylases and this induction is accompanied by chromatin remodeling at the hTERT promoter. Furthermore, we and others have shown that transiently transfected plasmid reporters are not ideal models for the repression of endogenous hTERT gene in somatic cells. Based on these findings, we hypothesize that chromatin environment is a critical component of the regulatory mechanisms for the repression of the native hTERT promoter. Here, we plan to study the molecular details of hTERT repression in a chromatin context using TPA-induced U937 cell differentiation as a model. We propose to pursue three interconnected aims: (1) To determine the role of global chromatin environment in hTERT repression during differentiation; (2) To determine sequential events of nuclear factor recruitment and histone modifications that occur at the hTERT core promoter region during differentiation. (3) To create a novel chromosome-based reporter system and dissect the roles of cis-regulatory elements in hTERT repression.

描述（由申请人提供）：我们的长期目标是了解发育过程中hTERT基因调控的关键步骤。编码人端粒酶限速亚基的hTERT基因在胚胎组织和干细胞中高水平表达，但在大多数成体体细胞中分化时被抑制。 虽然hTERT启动子已被广泛研究，染色质环境的贡献和要求的顺式元件尚未确定内源性hTERT转录的抑制。 以前的结果，包括我们自己的，已经表明，天然染色质在hTERT转录的调节中起着关键作用。 通过抑制组蛋白去乙酰化酶可以可逆地诱导hTERT转录，并且这种诱导伴随着hTERT启动子处的染色质重塑。 此外，我们和其他人已经表明，瞬时转染的质粒报告基因不是体细胞中内源性hTERT基因阻遏的理想模型。基于这些发现，我们推测染色质环境是天然hTERT启动子抑制的调控机制的关键组成部分。在这里，我们计划使用TPA诱导的U937细胞分化为模型，研究在染色质背景下hTERT抑制的分子细节。我们建议追求三个相互关联的目标：（1）以确定全球染色质环境的作用，在分化过程中的hTERT抑制;（2）以确定在分化过程中发生在hTERT核心启动子区域的核因子募集和组蛋白修饰的顺序事件。(3)建立一个新的基于染色体的报告系统，并分析顺式调控元件在hTERT抑制中的作用。