GLUCOCORTICOID ACTION IN SYNCHRONIZED CELLS

同步细胞中的糖皮质激素作用

• 批准号: 3230868
• 负责人: JOHN A. CIDLOWSKI
• 金额: $ 10.32万
• 依托单位: UNIV OF NORTH CAROLINA CHAPEL HILL
• 依托单位国家: 美国
• 财政年份: 1987
• 资助国家: 美国
• 起止时间: 1987-08-01 至 1992-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/3230868
• 关键词: HeLa cells; chromatin; density gradient ultracentrifugation; gel electrophoresis; gene expression; genetic manipulation; genetic regulation; genetic transcription; glucocorticoids; high performance liquid chromatography; histochemistry /cytochemistry; human tissue; messenger RNA; monoclonal antibody; nucleic acid sequence; phase contrast microscopy; synchronous cell division; tissue /cell culture; tritium

The goal of our research is to continue to explore the mechanisms of glucocorticoid hormone action during the cell cycle. Work in this and other laboratories has established that the progression of cells through the cell cycle results in significant alterations in glucocorticoid receptor number and structure. We will now focus our studies on the regulation of the glucocorticoid receptor gene during the cell cycle. The availability of cDNA clones of the human glucocorticoid receptor permits us to extend our analysis of receptor regulation to the molecular level. We hypothesize that changes in cellular glucocorticoid receptor number during the cell cycle can be accounted for by alteration in receptor gene regulation. To address this question we will evaluate glucocorticoid receptor mRNA accumulation, transcription and stability during the cell cycle. Concurrently the organizational structure of the glucocorticoid receptor gene will be assessed to determine what relationship, if any, exists between receptor gene transcription and receptor gene structure. Further studies will also be initiated to identify and characterize the DNA sequences necessary for glucocorticoid receptor gene expression. Finally we seek to evaluate further a recent observation made in our laboratory which demonstrates the interaction of the human glucocorticoid receptors with the coding domain of its gene. Specifically we will characterize by several criteria the interactions between glucocorticoid receptor and its own gene and evaluate in vivo the physiological significance of such interactions. Together the studies proposed in the application should lead to a better understanding of the mechanisms involved in the regulation of human glucocorticoid receptor gene expression.

我们的研究目标是继续探索其机制 糖皮质激素在细胞周期中的作用。 工作 这个实验室和其他实验室已经确定， 在细胞周期中的作用会导致 糖皮质激素受体的数量和结构。 我们现在将重点关注 糖皮质激素受体基因调控的研究 在细胞周期中。 利用cDNA克隆的方法， 人类糖皮质激素受体使我们能够扩展我们的分析 在分子水平上对受体的调节。 我们假设 细胞糖皮质激素受体数量的变化， 细胞周期可以通过受体基因的改变来解释 调控 为了解决这个问题，我们将评估 糖皮质激素受体mRNA积累、转录和 细胞周期中的稳定性。 同时，组织 糖皮质激素受体基因的结构将被评估， 确定受体基因之间存在什么关系，如果有的话， 转录和受体基因结构。 进一步的研究将 也开始识别和表征DNA序列 糖皮质激素受体基因表达所必需的。 最后我们 我想进一步评价我们最近在《宣言》中提出的一项意见， 实验室展示了人类的互动 糖皮质激素受体及其基因编码域。 具体来说，我们将通过几个标准来描述 糖皮质激素受体与自身基因的相互作用， 在体内评估这种生理意义， 交互. 申请中提出的研究 应有助于更好地了解所涉机制 在人糖皮质激素受体基因的调控中 表情