Lamphere L, Fiore F, Xu X, Brizuela L, Keezer S, Sardet C, Draetta G F, Gyuris J
Mitotix, Inc., Cambridge, Massachusetts 02139, USA.
Oncogene. 1997 Apr 24;14(16):1999-2004. doi: 10.1038/sj.onc.1201036.
Using the yeast two-hybrid system we have identified novel potential Cdk4 interacting proteins. Here we described the interaction of Cdk4 with a human homologue of the yeast Drosophila CDC37 gene products. Cdc37 protein specifically interacts with Cdk4 and Cdk6, but not with Cdc2, Cdk2, Cdk3, Cdk5 and any of a number of cyclins tested. Cdc37 is not an inhibitor nor an activator of the Cdk4/cyclin D1 kinase, while it appears to facilitate complex assembly between Cdk4, and cyclin D1 in vitro. Cdc37 competes with p16 for binding to Cdk4, suggesting that p16 might exert part of its inhibitory function by affecting the formation of Cdk4/cyclin D1 complexes via Cdc37.
利用酵母双杂交系统,我们鉴定出了新的潜在Cdk4相互作用蛋白。在此,我们描述了Cdk4与酵母果蝇CDC37基因产物的人类同源物之间的相互作用。Cdc37蛋白特异性地与Cdk4和Cdk6相互作用,但不与Cdc2、Cdk2、Cdk3、Cdk5以及所测试的多种细胞周期蛋白中的任何一种相互作用。Cdc37既不是Cdk4/细胞周期蛋白D1激酶的抑制剂也不是激活剂,而它似乎在体外促进了Cdk4与细胞周期蛋白D1之间的复合物组装。Cdc37与p16竞争结合Cdk4,这表明p16可能通过Cdc37影响Cdk4/细胞周期蛋白D1复合物的形成来发挥其部分抑制功能。