Contribution of time delays to p53 oscillation in DNA damage response

被引:1
|
作者
Wang, Conghua [1 ]
Liu, Haihong [2 ]
Zhou, Jin [1 ]
机构
[1] Shanghai Univ, Shanghai Inst Appl Math & Mech, Shanghai 200072, Peoples R China
[2] Yunnan Normal Univ, Dept Math, Kunming 650500, Yunnan, Peoples R China
基金
中国国家自然科学基金;
关键词
proteins; cellular biophysics; DNA; molecular biophysics; biomolecular effects of radiation; bifurcation; physiological models; cellular effects of radiation; oscillations; genetics; highlight; time delay; delayed negative feedback loops; murine double minute 2; Wip1 protein synthesis; explicit delays; Mdm2 protein synthesis; p53; network; PREDATOR-PREY MODEL; BIFURCATION-ANALYSIS; DYNAMICS; FEEDBACK; ATM; STABILITY; MECHANISM; PROTEIN; LOOP; MDM2;
D O I
10.1049/iet-syb.2019.0006
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Although the oscillatory dynamics of the p53 network have been extensively studied, the understanding of the mechanism of delay-induced oscillations is still limited. In this paper, a comprehensive mathematical model of p53 network is studied, which contains two delayed negative feedback loops. By studying the model with and without explicit delays, the results indicate that the time delay of Mdm2 protein synthesis can well control the pulse shape but cannot induce p53 oscillation alone, while the time delay required for Wip1 protein synthesis induces a Hopf bifurcation to drive p53 oscillation. In addition, the synergy of the two delays will cause the p53 network to oscillate in advance, indicating that p53 begins the repair process earlier in the damaged cell. Furthermore, the stability and bifurcation of the model are addressed, which may highlight the role of time delay in p53 oscillations.
引用
收藏
页码:180 / 185
页数:6
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