Department of Biology, Stanford University, Stanford, CA 94305, USA.
Department of Cell Biology & Green Center for Systems Biology, UT Southwestern Medical Center, Dallas, TX 75390, USA.
Mol Cell. 2018 Jan 18;69(2):253-264.e5. doi: 10.1016/j.molcel.2017.12.017.
At the restriction point (R), mammalian cells irreversibly commit to divide. R has been viewed as a point in G1 that is passed when growth factor signaling initiates a positive feedback loop of Cdk activity. However, recent studies have cast doubt on this model by claiming R occurs prior to positive feedback activation in G1 or even before completion of the previous cell cycle. Here we reconcile these results and show that whereas many commonly used cell lines do not exhibit a G1 R, primary fibroblasts have a G1 R that is defined by a precise Cdk activity threshold and the activation of cell-cycle-dependent transcription. A simple threshold model, based solely on Cdk activity, predicted with more than 95% accuracy whether individual cells had passed R. That a single measurement accurately predicted cell fate shows that the state of complex regulatory networks can be assessed using a few critical protein activities.
在限制点 (R),哺乳动物细胞不可逆地决定分裂。R 被视为 G1 中的一个点,当生长因子信号启动 Cdk 活性的正反馈循环时,细胞通过该点。然而,最近的研究对该模型提出了质疑,声称 R 发生在 G1 中的正反馈激活之前,甚至发生在完成前一个细胞周期之前。在这里,我们调和了这些结果,并表明,虽然许多常用的细胞系没有表现出 G1 R,但原代成纤维细胞具有 G1 R,该 R 由精确的 Cdk 活性阈值和细胞周期依赖性转录的激活来定义。一个简单的阈值模型,仅基于 Cdk 活性,以超过 95%的准确度预测单个细胞是否通过了 R。一个单一的测量可以准确地预测细胞命运,这表明复杂的调控网络的状态可以使用几个关键的蛋白质活性来评估。