Pursglove Sharon E, Mackay Joel P
School of Molecular and Microbial Biosciences, Building G08, University of Sydney, NSW 2006, Australia.
Int J Biochem Cell Biol. 2005 Dec;37(12):2472-7. doi: 10.1016/j.biocel.2005.06.013. Epub 2005 Jul 20.
CSL (CBF1, Suppressor of Hairless, Lag-1) is a transcription factor that is responsible for activating the genes downstream of the Notch signalling pathway, a pathway that is essential for the development of the nervous system and the differentiation of the haematopoietic system among others. In the absence of Notch signalling, CSL represses transcription of Notch target genes, and following activation by Notch, CSL is converted into a transcriptional activator and activates transcription of the same genes. These two opposing functions of CSL are mediated through interactions with distinct protein complexes. The Notch signalling pathway and its crucial cofactor CSL can maintain cells in an undifferentiated state, and have therefore been associated with a growing list of cancers. In addition, CSL has been co-opted by Epstein-Barr virus to mediate viral and host gene transcription following infection.
CSL(CBF1、无毛抑制因子、Lag-1)是一种转录因子,负责激活Notch信号通路下游的基因,该信号通路对神经系统发育以及造血系统分化等过程至关重要。在没有Notch信号时,CSL会抑制Notch靶基因的转录,而在被Notch激活后,CSL会转变为转录激活因子并激活相同基因的转录。CSL的这两种相反功能是通过与不同蛋白质复合物的相互作用来介导的。Notch信号通路及其关键辅因子CSL可使细胞维持在未分化状态,因此与越来越多的癌症相关。此外,爱泼斯坦-巴尔病毒在感染后利用CSL来介导病毒和宿主基因的转录。