Epigenetic Mechanisms of Toxicology Lab, MRC Toxicology Unit, Cambridge University, Cambridge CB2 1QR, UK.
Int J Mol Sci. 2020 Jul 28;21(15):5343. doi: 10.3390/ijms21155343.
Cyclin-dependent kinases (CDKs) and their inhibitors (CDKIs) play pivotal roles in the regulation of the cell cycle. As a result of these functions, it may be extrapolated that they are essential for appropriate embryonic development. The twenty known mouse CDKs and eight CDKIs have been studied to varying degrees in the developing mouse, but only a handful of CDKs and a single CDKI have been shown to be absolutely required for murine embryonic development. What has become apparent, as more studies have shone light on these family members, is that in addition to their primary functional role in regulating the cell cycle, many of these genes are also controlling specific cell fates by directing differentiation in various tissues. Here we review the extensive mouse models that have been generated to study the functions of CDKs and CDKIs, and discuss their varying roles in murine embryonic development, with a particular focus on the brain, pancreas and fertility.
细胞周期蛋白依赖性激酶(CDKs)及其抑制剂(CDKIs)在细胞周期调控中起着关键作用。由于这些功能,可以推断它们对于胚胎发育的正常进行是必不可少的。在发育中的小鼠中,对已知的 20 种小鼠 CDK 和 8 种 CDKIs 进行了不同程度的研究,但仅有少数 CDK 和一种 CDKI 被证明对小鼠胚胎发育是绝对必需的。随着更多的研究揭示了这些家族成员的作用,越来越明显的是,除了它们在调节细胞周期方面的主要功能外,许多这些基因还通过指导各种组织中的分化来控制特定的细胞命运。在这里,我们回顾了广泛的小鼠模型,这些模型被用来研究 CDK 和 CDKIs 的功能,并讨论了它们在小鼠胚胎发育中的不同作用,特别关注了大脑、胰腺和生育能力。