Nakayama K, Nakayama K
Department of Molecular and Cellular Biology, Kyushu University, Fukuoka, Japan.
Bioessays. 1998 Dec;20(12):1020-9. doi: 10.1002/(SICI)1521-1878(199812)20:12<1020::AID-BIES8>3.0.CO;2-D.
Precise control of cell-cycle progression is believed to be critical for normal development, while oncogenesis may be a direct result of its disturbance. Cell-cycle progression is regulated predominantly by a series of serine/threonine kinases, the cyclin-dependent kinases (CDKs). The activities of the CDKs are controlled by a variety of mechanisms, and a group of molecules that inhibit CDK activity, CDK inhibitors (CKIs), has recently become the focus of interest, particularly in the fields of development and tumorigenesis. To date, seven CKIs have been identified in mammals and categorized into two families, the Cip/Kip and Ink4 families. The Cip/Kip family is well conserved phylogenetically, suggesting that it is biologically important. Despite the structural and biochemical similarities among the Cip/Kip members, the phenotypes of knockout mice of each Cip/Kip member are surprisingly different, which suggests that the Cip/Kip CKIs have a variety of physiological functions. In this review, the biological roles of Cip/Kip CKIs in development and tumor suppression are discussed.
细胞周期进程的精确调控被认为对正常发育至关重要,而肿瘤发生可能是其紊乱的直接结果。细胞周期进程主要由一系列丝氨酸/苏氨酸激酶,即细胞周期蛋白依赖性激酶(CDK)调控。CDK的活性受多种机制控制,一类抑制CDK活性的分子,即CDK抑制剂(CKI),最近成为了研究热点,尤其是在发育和肿瘤发生领域。迄今为止,在哺乳动物中已鉴定出7种CKI,并分为两个家族,即Cip/Kip家族和Ink4家族。Cip/Kip家族在系统发育上高度保守,表明其具有重要生物学意义。尽管Cip/Kip家族成员在结构和生化方面存在相似性,但每个Cip/Kip家族成员的基因敲除小鼠的表型却惊人地不同,这表明Cip/Kip CKI具有多种生理功能。在这篇综述中,我们将讨论Cip/Kip CKI在发育和肿瘤抑制中的生物学作用。