Herzinger T, Reed S I
Department of Molecular Biology, The Scripps Research Institute, La Jolla, California 92037, USA.
J Biol Chem. 1998 Jun 12;273(24):14958-61. doi: 10.1074/jbc.273.24.14958.
D-type cyclins are induced in response to mitogens and are believed to control progression through the G1 phase of the cell cycle by activating their corresponding kinase partners (cyclin-dependent kinases). To investigate the function of individual D-type cyclins we have constructed rat fibroblast lines that allow controllable overexpression of a human cyclin D3 cDNA. Overexpression of cyclin D3 led to accelerated passage through G1 in actively proliferating cells with no effect on the overall population doubling time. In cells re-entering the division cycle from a quiescent state, cyclin D3 caused an even more dramatic advancement of S phase entry. Accelerated progression through G0/G1-to-S correlated with premature phosphorylation of the pRb tumor suppressor protein and its relatives, p107 and p130. We conclude that cyclin D3 can act as a rate-limiting G1 cyclin and that this effect involves, in part, the premature phosphorylation of critical substrates.
D型细胞周期蛋白是在有丝分裂原的作用下被诱导产生的,据信它们通过激活相应的激酶伴侣(细胞周期蛋白依赖性激酶)来控制细胞周期G1期的进程。为了研究单个D型细胞周期蛋白的功能,我们构建了大鼠成纤维细胞系,该细胞系可可控地过表达人细胞周期蛋白D3 cDNA。细胞周期蛋白D3的过表达导致活跃增殖细胞在G1期的进程加速,而对总体群体倍增时间没有影响。在从静止状态重新进入分裂周期的细胞中,细胞周期蛋白D3使S期进入的进程更加显著地提前。通过G0/G1到S期的加速进程与pRb肿瘤抑制蛋白及其相关蛋白p107和p130的过早磷酸化相关。我们得出结论,细胞周期蛋白D3可以作为一种G1期的限速细胞周期蛋白,并且这种作用部分涉及关键底物的过早磷酸化。