O'Connell Brenda C, Harper J Wade
Department of Pathology, Harvard Medical School, 77 Ave Louis Pasteur, Boston, MA 02115, USA.
Curr Opin Cell Biol. 2007 Apr;19(2):206-14. doi: 10.1016/j.ceb.2007.02.014. Epub 2007 Feb 20.
Cul4-Ddb1, a RING H2 ubiquitin ligase, plays an important role in many vital cellular processes including DNA replication, DNA repair and transcription. Recent research reveals strong links between Cul4-mediated signaling pathways and chromatin biology. Ubiquitylation of substrates by Cul4-Ddb1 occurs on chromatin and is initiated by chromatin-based signals that either recruit Cul4-Ddb1 to chromatin or alter the activity of the ligase. This includes Cul4-mediated ubiquitylation of the replication licensing factor, Cdt1; a process that requires chromatin-bound PCNA and Cdt2, a member of the recently identified family of candidate substrate receptors for Cul4 (termed Ddb1- and Cul4-associated factors: DCAFs). The activity of two other Cul4-based ubiquitin ligases, Cul4-Ddb1(Ddb2) and Cul4-Ddb1(CSA), are differentially regulated by the COP9 signalosome in response to different chromatin-based signals. Finally, examples of direct modifications to chromatin by Cul4-Ddb1 have emerged, including ubiquitylation of histones and the recruitment of enzymes involved in chromatin remodeling or histone methylation.
Cul4-Ddb1是一种RING H2泛素连接酶,在包括DNA复制、DNA修复和转录在内的许多重要细胞过程中发挥着重要作用。最近的研究揭示了Cul4介导的信号通路与染色质生物学之间的紧密联系。Cul4-Ddb1对底物的泛素化作用发生在染色质上,并由基于染色质的信号启动,这些信号要么将Cul4-Ddb1招募到染色质上,要么改变连接酶的活性。这包括Cul4介导的复制许可因子Cdt1的泛素化;这一过程需要与染色质结合的增殖细胞核抗原(PCNA)和Cdt2,Cdt2是最近鉴定出的Cul4候选底物受体家族(称为Ddb1和Cul4相关因子:DCAFs)的成员。另外两种基于Cul4的泛素连接酶Cul4-Ddb1(Ddb2)和Cul4-Ddb1(CSA)的活性,会受到COP9信号小体的不同调节,以响应不同的基于染色质的信号。最后,已经出现了Cul4-Ddb1对染色质进行直接修饰的例子,包括组蛋白的泛素化以及参与染色质重塑或组蛋白甲基化的酶的募集。