Department of Molecular Genetics, University of Toronto, Toronto, ON M5G 1A8, Canada; Cell Biology, The Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.
Cell Biology, The Hospital for Sick Children, Toronto, ON M5G 0A4, Canada.
Dev Cell. 2021 Jun 21;56(12):1756-1769.e7. doi: 10.1016/j.devcel.2021.04.030. Epub 2021 May 21.
While molecules that promote the growth of animal cells have been identified, it remains unclear how such signals are orchestrated to determine a characteristic target size for different cell types. It is increasingly clear that cell size is determined by size checkpoints-mechanisms that restrict the cell cycle progression of cells that are smaller than their target size. Previously, we described a p38 MAPK-dependent cell size checkpoint mechanism whereby p38 is selectively activated and prevents cell cycle progression in cells that are smaller than a given target size. In this study, we show that the specific target size required for inactivation of p38 and transition through the cell cycle is determined by CDK4 activity. Our data suggest a model whereby p38 and CDK4 cooperate analogously to the function of a thermostat: while p38 senses irregularities in size, CDK4 corresponds to the thermostat dial that sets the target size.
虽然已经鉴定出促进动物细胞生长的分子,但尚不清楚这些信号是如何协调的,以确定不同细胞类型的特征靶大小。越来越明显的是,细胞大小是由大小检查点决定的——这些机制限制了小于目标大小的细胞的细胞周期进程。此前,我们描述了一种依赖于 p38 MAPK 的细胞大小检查点机制,其中 p38 被选择性激活,并阻止小于给定目标大小的细胞的细胞周期进程。在这项研究中,我们表明,失活 p38 和通过细胞周期过渡所需的特定目标大小由 CDK4 活性决定。我们的数据表明了一种模型,其中 p38 和 CDK4 类似于恒温器的功能进行合作:虽然 p38 感知大小的不规则性,但 CDK4 对应于设置目标大小的恒温器刻度盘。