CDK4/6 活性的瞬时滞后导致 G1 期限制点的通过。
Transient Hysteresis in CDK4/6 Activity Underlies Passage of the Restriction Point in G1.
机构信息
Department of Chemical and Systems Biology, Stanford University School of Medicine, 318 Campus Drive, Clark Building W200, Stanford, CA 94305, USA.
Department of Chemical and Systems Biology, Stanford University School of Medicine, 318 Campus Drive, Clark Building W200, Stanford, CA 94305, USA; Department of Pathology and Cell Biology, Columbia University Medical Center, New York, NY, USA.
出版信息
Mol Cell. 2019 Nov 21;76(4):562-573.e4. doi: 10.1016/j.molcel.2019.08.020. Epub 2019 Sep 19.
Cells escape the need for mitogens at a restriction point several hours before entering S phase. The restriction point has been proposed to result from CDK4/6 initiating partial Rb phosphorylation to trigger a bistable switch whereby cyclin E-CDK2 and Rb mutually reinforce each other to induce Rb hyperphosphorylation. Here, using single-cell analysis, we unexpectedly found that cyclin E/A-CDK activity can only maintain Rb hyperphosphorylation starting at the onset of S phase and that CDK4/6 activity, but not cyclin E/A-CDK activity, is required to hyperphosphorylate Rb throughout G1 phase. Mitogen removal in G1 results in a gradual loss of CDK4/6 activity with a high likelihood of cells sustaining Rb hyperphosphorylation until S phase, at which point cyclin E/A-CDK activity takes over. Thus, it is short-term memory, or transient hysteresis, in CDK4/6 activity following mitogen removal that sustains Rb hyperphosphorylation, demonstrating a probabilistic rather than an irreversible molecular mechanism underlying the restriction point.
细胞在进入 S 期前数小时就摆脱了有丝分裂原的需求,在限制点上。限制点被提出是由于 CDK4/6 引发部分 Rb 磷酸化,触发双稳态开关,使细胞周期蛋白 E-CDK2 和 Rb 相互加强,从而诱导 Rb 高度磷酸化。在这里,我们使用单细胞分析,出乎意料地发现,只有在 S 期开始时,细胞周期蛋白 E/A-CDK 活性才能维持 Rb 的高度磷酸化,而 CDK4/6 活性,而不是细胞周期蛋白 E/A-CDK 活性,在整个 G1 期都需要使 Rb 高度磷酸化。在 G1 期去除有丝分裂原会导致 CDK4/6 活性逐渐丧失,细胞很有可能维持 Rb 高度磷酸化,直到 S 期,此时细胞周期蛋白 E/A-CDK 活性接管。因此,是 CDK4/6 活性在有丝分裂原去除后的短期记忆或短暂滞后维持了 Rb 的高度磷酸化,这表明限制点的分子机制是概率性的,而不是不可逆的。