Ray Arpita, James Melissa K, Larochelle Stéphane, Fisher Robert P, Blain Stacy W
Program in Molecular and Cellular Biology, School of Graduate Studies, SUNY Downstate Medical Center, Brooklyn, New York 11203, USA.
Mol Cell Biol. 2009 Feb;29(4):986-99. doi: 10.1128/MCB.00898-08. Epub 2008 Dec 15.
Cell cycle progression is regulated by cyclin-dependent kinases (cdk's), which in turn are regulated by their interactions with stoichiometric inhibitors, such as p27(Kip1). Although p27 associates with cyclin D-cyclin-dependent kinase 4 (cdk4) constitutively, whether or not it inhibits this complex is dependent on the absence or presence of a specific tyrosine phosphorylation that converts p27 from a bound inhibitor to a bound noninhibitor under different growth conditions. This phosphorylation occurs within the 3-10 helix of p27 and may dislodge the helix from cdk4's active site to allow ATP binding. Here we show that the interaction of nonphosphorylated p27 with cdk4 also prevents the activating phosphorylation of the T-loop by cyclin H-cdk7, the cdk-activating kinase (CAK). Even though the cyclin H-cdk7 complex is present and active in contact-arrested cells, p27's association with cyclin D-cdk4 prevents T-loop phosphorylation. When p27 is tyrosine phosphorylated in proliferating cells or in vitro with the tyrosine Y kinase Abl, phosphorylation of cdk4 by cyclin H-cdk7 is permitted, even without dissociation of p27. This suggests that upon release from the contact-arrested state, a temporal order for the reactivation of inactive p27-cyclin D-cdk4 complexes must exist: p27 must be Y phosphorylated first, directly permitting cyclin H-cdk7 phosphorylation of residue T172 and the consequent restoration of kinase activity. The non-Y-phosphorylated p27-cyclin D-cdk4 complex could be phosphorylated by purified Csk1, a single-subunit CAK from fission yeast, but was still inactive due to p27's occlusion of the active site. Thus, the two modes by which p27 inhibits cyclin D-cdk4 are independent and may reinforce one another to inhibit kinase activity in contact-arrested cells, while maintaining a reservoir of preformed complex that can be activated rapidly upon cell cycle reentry.
细胞周期进程受细胞周期蛋白依赖性激酶(CDK)调控,而CDK又受其与化学计量抑制剂(如p27^(Kip1))相互作用的调节。尽管p27持续与细胞周期蛋白D - 细胞周期蛋白依赖性激酶4(CDK4)结合,但它是否抑制该复合物取决于特定酪氨酸磷酸化的有无,这种磷酸化在不同生长条件下可将p27从结合的抑制剂转变为结合的非抑制剂。这种磷酸化发生在p27的3 - 10螺旋内,可能使该螺旋从CDK4的活性位点脱离以允许ATP结合。我们在此表明,非磷酸化的p27与CDK4的相互作用还可阻止细胞周期蛋白H - CDK7(即CDK激活激酶(CAK))对T环的激活磷酸化。尽管细胞周期蛋白H - CDK7复合物在接触抑制的细胞中存在且有活性,但p27与细胞周期蛋白D - CDK4的结合会阻止T环磷酸化。当p27在增殖细胞中或在体外被酪氨酸激酶Abl进行酪氨酸磷酸化时,即使p27不解离,细胞周期蛋白H - CDK7也能对CDK4进行磷酸化。这表明从接触抑制状态释放后,失活的p27 - 细胞周期蛋白D - CDK4复合物重新激活必然存在一个时间顺序:p27必须首先被Y磷酸化,直接允许细胞周期蛋白H - CDK7对T172位点进行磷酸化并随之恢复激酶活性。非Y磷酸化的p27 - 细胞周期蛋白D - CDK4复合物可被来自裂殖酵母的单亚基CAK即纯化的Csk1磷酸化,但由于p27对活性位点的封闭,其仍无活性。因此,p27抑制细胞周期蛋白D - CDK4的两种方式相互独立,可能相互加强以抑制接触抑制细胞中的激酶活性,同时维持一个预先形成的复合物储备,该储备在细胞周期重新进入时可迅速被激活。