Lai Eric C
Department of Molecular and Cell Biology, University of California, Berkeley, 94720-3200, USA.
EMBO Rep. 2002 Sep;3(9):840-5. doi: 10.1093/embo-reports/kvf170.
CSL [CBF-1, Su(H), Lag-1]-type transcription factors are the primary effectors of the Notch pathway, a signal transduction cascade that is essential for the development of all metazoan organisms. Interestingly, CSL proteins were originally classified as transcriptional repressors in vertebrates, but as transcriptional activators in model invertebrate organisms. Resolution of this paradox came with the realization that repression and activation by CSL proteins occurs in both systems and that the switch involves recruitment of distinct co-repressor and co-activator complexes. Although CSL proteins appear to utilize a common co-activator complex of largely similar constitution, recent studies have demonstrated that vertebrate and Drosophila CSL interact with a variety of distinct co-repressor complexes. This review highlights differences in composition and similarities in function of different CSL co-repressor complexes, which actively repress Notch pathway target genes in the absence of Notch pathway activity.
CSL[CBF-1、Su(H)、Lag-1]型转录因子是Notch信号通路的主要效应因子,Notch信号通路是一种信号转导级联反应,对所有后生动物的发育至关重要。有趣的是,CSL蛋白最初在脊椎动物中被归类为转录抑制因子,而在模式无脊椎动物中则被归类为转录激活因子。随着人们认识到CSL蛋白在这两种系统中都能发生抑制和激活作用,且这种转变涉及不同共抑制因子和共激活因子复合物的募集,这一矛盾得以解决。尽管CSL蛋白似乎利用了一种组成基本相似的常见共激活因子复合物,但最近的研究表明,脊椎动物和果蝇的CSL与多种不同的共抑制因子复合物相互作用。本综述着重介绍了不同CSL共抑制因子复合物在组成上的差异及其功能上的相似性,这些复合物在Notch信号通路无活性时可积极抑制Notch信号通路的靶基因。