Gastwirt Randy F, McAndrew Christopher W, Donoghue Daniel J
Biomedical Sciences Program, Department of Chemistry and Biochemistry, University of California San Diego, La Jolla, California, USA.
Cell Cycle. 2007 May 15;6(10):1188-93. doi: 10.4161/cc.6.10.4252. Epub 2007 May 5.
Speedy/RINGO family members bind and activate cyclin dependent kinases (CDKs), although these proteins have no homology to known cyclin proteins. Members of this family are required for and enhance meiotic maturation, in addition to having novel roles in regulating the mitotic mammalian cell cycle and the DNA damage response. Here we discuss how the specialized functions of these proteins differ from classical cyclin-mediated activation of CDKs. Through atypical activation of CDKs, bypass of conventional inhibitory mechanisms, and unique substrate selection, Speedy/RINGO proteins contribute to cell cycle, checkpoint, and apoptotic regulation. Furthermore, we address the recently established correlation between Spy1 and cancer in terms of the specialized functions of the Speedy/RINGO family.
Speedy/RINGO家族成员能够结合并激活细胞周期蛋白依赖性激酶(CDK),尽管这些蛋白质与已知的细胞周期蛋白没有同源性。除了在调节有丝分裂的哺乳动物细胞周期和DNA损伤反应中发挥新作用外,该家族成员还是减数分裂成熟所必需的,并能促进减数分裂成熟。在这里,我们将讨论这些蛋白质的特殊功能与经典的细胞周期蛋白介导的CDK激活有何不同。通过CDK的非典型激活、绕过传统的抑制机制以及独特的底物选择,Speedy/RINGO蛋白有助于细胞周期、检查点和细胞凋亡的调节。此外,我们还将根据Speedy/RINGO家族的特殊功能,探讨最近发现的Spy1与癌症之间的关联。