Pagano M, Pepperkok R, Lukas J, Baldin V, Ansorge W, Bartek J, Draetta G
Differentiation Programme, European Molecular Biology Laboratory, Heidelberg, Germany.
J Cell Biol. 1993 Apr;121(1):101-11. doi: 10.1083/jcb.121.1.101.
In mammalian cells inhibition of the cdc2 function results in arrest in the G2-phase of the cell cycle. Several cdc2-related gene products have been identified recently and it has been hypothesized that they control earlier cell cycle events. Here we have studied the relationship between activation of one of these cdc2 homologs, the cdk2 protein kinase, and the progression through the cell cycle in cultured human fibroblasts. We found that cdk2 was activated and specifically localized to the nucleus during S phase and G2. Microinjection of affinity-purified anti-cdk2 antibodies but not of affinity-purified anti-cdc2 antibodies, during G1, inhibited entry into S phase. The specificity of these effects was demonstrated by the fact that a plasmid-driven cdk2 overexpression counteracted the inhibition. These results demonstrate that the cdk2 protein kinase is involved in the activation of DNA synthesis.
在哺乳动物细胞中,对cdc2功能的抑制会导致细胞周期停滞于G2期。最近已鉴定出几种与cdc2相关的基因产物,并且据推测它们控制着细胞周期中更早的事件。在此,我们研究了这些cdc2同源物之一,即cdk2蛋白激酶的激活与培养的人成纤维细胞中细胞周期进程之间的关系。我们发现,cdk2在S期和G2期被激活并特异性定位于细胞核。在G1期显微注射亲和纯化的抗cdk2抗体而非亲和纯化的抗cdc2抗体,会抑制细胞进入S期。质粒驱动的cdk2过表达可抵消这种抑制作用,这一事实证明了这些效应的特异性。这些结果表明,cdk2蛋白激酶参与了DNA合成的激活。