Malumbres Marcos, Barbacid Mariano
Molecular Oncology Programme, Centro Nacional de Investigaciones Oncológicas, Melchor Fernández Almagro 3, E-28029 Madrid, Spain.
Trends Biochem Sci. 2005 Nov;30(11):630-41. doi: 10.1016/j.tibs.2005.09.005. Epub 2005 Oct 19.
Cyclin-dependent kinases (Cdks) are the catalytic subunits of a family of mammalian heterodimeric serine/threonine kinases that have been implicated in the control of cell-cycle progression, transcription and neuronal function. Recent genetic evidence obtained with gene-targeted mice has shown that Cdk4 and Cdk6 are not needed for entry into the cell cycle after mitogenic stimuli and organogenesis; however, they are essential for the proliferation of some endocrine and hematopoietic cells. Cdk2 is also dispensable for the mitotic cell cycle. Indeed, mice without Cdk2 are normal except for their complete sterility: unexpectedly, Cdk2 is crucial for the first meiotic division of male and female germ cells. These findings have important implications both for our current understanding of the role of Cdks in regulating the mammalian cell cycle and for their potential use as therapeutic targets in cancer.
细胞周期蛋白依赖性激酶(Cdks)是一类哺乳动物异二聚体丝氨酸/苏氨酸激酶家族的催化亚基,这些激酶与细胞周期进程、转录和神经元功能的调控有关。最近通过基因靶向小鼠获得的遗传学证据表明,有丝分裂原刺激和器官发生后进入细胞周期不需要Cdk4和Cdk6;然而,它们对于某些内分泌和造血细胞的增殖至关重要。Cdk2对于有丝分裂细胞周期也是可有可无的。事实上,没有Cdk2的小鼠除了完全不育外是正常的:出乎意料的是,Cdk2对于雄性和雌性生殖细胞的第一次减数分裂至关重要。这些发现对于我们目前对Cdks在调节哺乳动物细胞周期中的作用的理解以及它们作为癌症治疗靶点的潜在用途都具有重要意义。