ZEB/deltaEF1 and Estrogen Signaling Cascades

超出所提供的空间。除了正常的生理功能外，雌激素还指导着导致许多病理状况的保护和促进的事件。然而，将受体与其靶基因的结合与最终生物学后果联系起来的分子细节往往仍不清楚。为了定义雌激素触发的信号级联反应，研究人员发现，ZEB/rEF1基因在转录水平上受到雌激素的诱导。另有数据显示，ZEB/rEF1是生殖组织雌激素信号转导通路中的一个环节。例如，在快速增殖的子宫内膜癌和卵巢癌中，ZEB/rEF1的表达量很高，但不再受雌激素的调节。相反，在生长缓慢的子宫内膜癌中，该基因被删除。这些数据表明ZEB/rEF1在生殖组织中起着关键作用。ZEB/rEF1是一种转录因子，它包含几个功能域，包括在每个末端的两个锌指簇。大多数数据表明，ZEB/fEF1是一种转录抑制因子，但在某些情况下，它也起到转录激活因子的作用。本课题的总体目标是明确ZEB/rEF1激活基因的机制，并鉴定其靶基因。本课题的具体目的是：1)研究ZEB/SEF1的基因激活机制；2)鉴定生殖组织中与ZEB_EF1共激活因子的蛋白；3)鉴定ZEB/fEF1在乳腺癌细胞系中的下游靶点。第一个目标将主要通过截断ZEB/rEF1并确定对报告基因激活的影响来实现。第二个具体目标将通过两种互补的方法，串联质谱法和酵母双杂交Ras招募系统来解决。对于最后一个特定目的，ZEB/rEF1的靶基因将使用DNA微阵列基因谱分析来鉴定。这些实验将为了解ZEB/rEF1基因激活机制和雌激素信号转导途径提供重要信息。网站性能 ======================================== 节结束 ===========================================

EXCEED THE SPACE PROVIDED. In addition to its normal physiological functions, estrogen directs events that lead to both the protection from and promotion of many pathological conditions. However, the molecular details linking the binding of the receptor to its target genes with the ultimate biological consequence often remain unclear. In an attempt to define signaling cascades triggered by estrogen, the novel observation was made that the ZEB/rEF1 gene is induced at the transcriptional level by estrogen. Other data show that ZEB/rEF1 is one of the links in estrogen signal transduction pathways in reproductive tissues. For example, ZEB/rEF1 expression is high in rapidly proliferating endometrial and ovarian cancers but is no longer regulated by estrogen. In contrast, the gene is deleted in slowly growing endometrial cancers. These data suggest that ZEB/rEF1 plays a pivotal role in reproductive tissues. ZEB/rEF1 is a transcription factor that contains several functional domains including two zinc finger clusters at each terminus. Most data suggest that ZEB/fEF1 is a transcriptional repressor but in some circumstances it functions as a transcriptional activator. The overall goals of this proposal are to define the mechanism of gene activation by ZEB/rEF1 and to identify its target genes. The specific aims of this proposal are to 1). investigate the mechanism of gene activation by ZEB/SEF1, 2). identify the proteins in reproductive tissues that act as co-activators with ZEB_EF1, and 3). identify the downstream targets of ZEB/fEF1 in a breast cancer cell line. The first aim will be approached primarily by truncating ZEB/rEF1 and determining the effects on reporter gene activation. The second specific aim will be addressed by two complementary approaches, tandem mass spectrometry and a yeast two-hybrid Ras recruitment system. For the last specific aim, target genes for ZEB/rEF1 will be identified using gene profiling with DNA microarrays. These experiments will provide important information about the mechanism of gene activation by ZEB/rEF1 and about estrogen signal transduction pathways. PERFORMANCE SITE ========================================Section End===========================================