Eliaš Ján, Dimitrio Luna, Clairambault Jean, Natalini Roberto
UPMC, Laboratoire Jacques-Louis Lions, 4 Place Jussieu, F-75005 Paris, France & INRIA Paris-Rocquencourt, MAMBA project-team, Paris and Rocquencourt, France.
Phys Biol. 2014 Aug;11(4):045001. doi: 10.1088/1478-3975/11/4/045001. Epub 2014 Jul 30.
The intracellular signalling network of the p53 protein plays important roles in genome protection and the control of cell cycle phase transitions. Recently observed oscillatory behaviour in single cells under stress conditions has inspired several research groups to simulate and study the dynamics of the protein with the aim of gaining a proper understanding of the physiological meanings of the oscillations. We propose compartmental ODE and PDE models of p53 activation and regulation in single cells following DNA damage and we show that the p53 oscillations can be retrieved by plainly involving p53-Mdm2 and ATM-p53-Wip1 negative feedbacks, which are sufficient for oscillations experimentally, with no further need to introduce any delays into the protein responses and without considering additional positive feedback.
p53蛋白的细胞内信号网络在基因组保护和细胞周期阶段转换的控制中发挥着重要作用。最近在应激条件下单细胞中观察到的振荡行为激发了几个研究小组对该蛋白动力学进行模拟和研究,目的是正确理解振荡的生理意义。我们提出了DNA损伤后单细胞中p53激活和调控的隔室常微分方程(ODE)和偏微分方程(PDE)模型,并且我们表明,通过简单地涉及p53-Mdm2和ATM-p53-Wip1负反馈就可以恢复p53振荡,这在实验上足以产生振荡,无需进一步在蛋白反应中引入任何延迟,也无需考虑额外的正反馈。