Decision making of the p53 network: death by integration.
Decision making of the p53 network: death by integration.
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DOI:
10.1016/j.jtbi.2010.11.041
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发表时间:
2011-02-21
影响因子:
2
通讯作者:
Tang, Chao
中科院分区:
文献类型:
--
作者:
Li, Zhiyuan;Ni, Ming;Li, Jikun;Zhang, Yuping;Ouyang, Qi;Tang, Chao
The tumor suppressor protein p53 plays a central role in the multiple response pathways activated by DNA damage. In particular, p53 is involved in both the pro-survival response of cell cycle arrest and DNA repair, and the pro-death response of apoptosis. How does the p53 network coordinate the different pathways that lead to the opposite cell fates and what is its strategy in making the life-death decisions? To address these questions, we develop an integrated mathematical model that embraces three key modules of the p53 network: p53 core regulation, p53-induced cell cycle arrest and p53-dependent apoptosis initiation. Our analyses reveal that different aspects of the nuclear p53 dynamic profile are being used to differentially regulate the pro-survival and the pro-death modules. While the activation of the pro-survival module is dependent on the current or recent status of the DNA damage, the activation of the pro-death module relies on the accumulation or integration of the damage level over time. Thus, the cell will take the death fate if it cannot recover from the damage within a time period that is inversely proportional to the damage level. This “adaptive timer” strategy is likely to be adopted in other stress response systems.
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影响因子:
8
作者:
He, GG;Siddik, ZH;Kuang, J
通讯作者:
Kuang, J
影响因子:
3.4
作者:
Bagci, EZ;Vodovotz, Y;Bahar, I
通讯作者:
Bahar, I
DOI:
10.1126/science.1164860
发表时间:
2009-04-10
期刊:
Science (New York, N.Y.)
影响因子:
--
作者:
Ashall L;Horton CA;Nelson DE;Paszek P;Harper CV;Sillitoe K;Ryan S;Spiller DG;Unitt JF;Broomhead DS;Kell DB;Rand DA;Sée V;White MR
通讯作者:
White MR
影响因子:
56.9
作者:
Hoffmann, A;Levchenko, A;Baltimore, D
通讯作者:
Baltimore, D
影响因子:
16
作者:
Batchelor, Eric;Mock, Caroline S.;Lahav, Galit
通讯作者:
Lahav, Galit