Jin Jianping, Arias Emily E, Chen Jing, Harper J Wade, Walter Johannes C
Department of Pathology, Harvard Medical School, Boston, Massachusetts 02115, USA.
Mol Cell. 2006 Sep 1;23(5):709-21. doi: 10.1016/j.molcel.2006.08.010.
Cul4 E3 ubiquitin ligases contain the cullin 4 scaffold and the triple beta propeller Ddb1 adaptor protein, but few substrate receptors have been identified. Here, we identify 18 Ddb1- and Cul4-associated factors (DCAFs), including 14 containing WD40 repeats. DCAFs interact with multiple surfaces on Ddb1, and the interaction of WD40-containing DCAFs with Ddb1 requires a conserved "WDXR" motif. DCAF2/Cdt2, which is related to S. pombe Cdt2, functions in Xenopus egg extracts and human cells to destroy the replication licensing protein Cdt1 in S phase and after DNA damage. Depletion of human Cdt2 causes rereplication and checkpoint activation. In Xenopus, Cdt2 is recruited to replication forks via Cdt1 and PCNA, where Cdt1 ubiquitylation occurs. These studies uncover diverse substrate receptors for Cul4 and identify Cdt2 as a conserved component of the Cul4-Ddb1 E3 that is essential to destroy Cdt1 and ensure proper cell cycle regulation of DNA replication.
Cul4 E3泛素连接酶包含cullin 4支架和三β螺旋桨Ddb1衔接蛋白,但已鉴定出的底物受体很少。在此,我们鉴定出18种Ddb1和Cul4相关因子(DCAFs),其中14种含有WD40重复序列。DCAFs与Ddb1的多个表面相互作用,含WD40的DCAFs与Ddb1的相互作用需要一个保守的“WDXR”基序。与粟酒裂殖酵母Cdt2相关的DCAF2/Cdt2在非洲爪蟾卵提取物和人类细胞中发挥作用,在S期及DNA损伤后破坏复制许可蛋白Cdt1。人类Cdt2的缺失会导致再复制和检查点激活。在非洲爪蟾中,Cdt2通过Cdt1和增殖细胞核抗原被招募到复制叉,在那里发生Cdt1的泛素化。这些研究揭示了Cul4的多种底物受体,并确定Cdt2是Cul4-Ddb1 E3的一个保守成分,对破坏Cdt1和确保DNA复制的正确细胞周期调控至关重要。