Mechanisms of Transcriptional Regulation in Stem Cells

描述（由申请人提供）：干细胞必须处理两个关键的，但相反的力量;需要持续自我更新和响应分化信号的能力与基因表达的大规模变化。许多研究已经证实，细胞增殖和分化的调控受到染色质结构的严重影响。本提案的总体目标是确定负责建立和维持干细胞中活性和非活性染色质模式以及基因表达模式的分子机制。这项建议的一个高度创新的方面是染色质免疫沉淀与几种不同类型的小鼠基因组微阵列的使用相结合。第一组阵列将包含斑点状CpG岛和其他在小鼠和人类基因组之间保守的调控区。第二种类型的阵列将由包含整个小鼠染色体的寡核苷酸组成。我们将开始我们的研究，通过使用阵列来识别活性与非活性启动子，使用RNA聚合酶II和修饰的组蛋白的抗体（目的1）。我们将测试不同形式的基因调控在胚胎干细胞和胚状体中占主导地位的假设。这些实验将提供未分化与分化胚胎干细胞中活性与非活性染色质的量和位置的全局快照，并且还将提供关于哪些基因以分化特异性方式打开和关闭的信息。在目标2A中，我们将鉴定Oct 4的靶基因，Oct 4是一种已知对维持ES细胞多能性至关重要的转录因子。在确定Oct 4靶基因后，我们将描述Oct 4调节这些基因的机制，特别是测试Oct 4在ES细胞中作为转录抑制因子的假设。在目标1中获得的关于活性与非活性染色质特征的知识对于这些研究至关重要。在目标2B中，我们将描述负责Oct 4基因的干细胞特异性调控的分子机制。

DESCRIPTION (provided by applicant): Stem cells must deal with two critical, yet opposing, forces; the need for continual self-renewal and the ability to respond to differentiation signals with large scale changes in gene expression. Many studies have established that regulation of proliferation and differentiation is heavily influenced by chromatin structure. The overall goals of this proposal are to determine the molecular mechanisms responsible for establishing and maintaining patterns of active and inactive chromatin, and thus patterns of gene expression, in stem cells. A highly innovative aspect of this proposal is the combination of chromatin immunoprecipitation with the use of several different types of mouse genomic microarrays. The first set of arrays will contain spotted CpG islands and other regulatory regions that are conserved between the mouse and human genomes. The second type of array will consist of oligonucleotides that encompass an entire mouse chromosome. We will begin our studies by employing the arrays to identify active vs. inactive promoters, using antibodies to RNA polymerase II and modified histones (Aim 1). We will test the hypothesis that different forms of gene regulation predominate in embryonic stem cells vs. in embryoid bodies. These experiments will provide a global snapshot of the amount and location of active vs. inactive chromatin in undifferentiated vs. differentiating embryonic stem cells and will also provide information as to which genes turn on and off in a differentiation-specific manner. In Aim 2A, we will identify targets genes of Oct4, a transcription factor that is known to be critical for maintaining pluripotency of ES cells. After identification of Oct4 target genes, we will characterize the mechanisms by which Oct4 regulates these genes, specifically testing the hypothesis that Oct4 functions as a transcriptional repressor in ES cells. The knowledge gained in Aim 1 concerning the characteristics of active vs. inactive chromatin will be critical for these studies. In Aim 2B, we will characterize the molecular mechanisms responsible for the stem cell-specific regulation of the Oct4 gene.