Dynamics of the p53-Mdm2 feedback loop in individual cells

被引:787
作者
Lahav, G
Rosenfeld, N
Sigal, A
Geva-Zatorsky, N
Levine, AJ
Elowitz, MB
Alon, U [1 ]
机构
[1] Weizmann Inst Sci, Dept Mol Cell Biol, IL-76100 Rehovot, Israel
[2] Weizmann Inst Sci, Dept Phys Complex Syst, IL-76100 Rehovot, Israel
[3] Inst Adv Studies, Sch Nat Sci, Princeton, NJ 08540 USA
[4] CALTECH, Div Biol, Pasadena, CA 91125 USA
基金
以色列科学基金会;
关键词
D O I
10.1038/ng1293
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The tumor suppressor p53, one of the most intensely investigated proteins(1-5), is usually studied by experiments that are averaged over cell populations, potentially masking the dynamic behavior in individual cells. We present a system for following, in individual living cells, the dynamics of p53 and its negative regulator Mdm2 (refs.1, 4-7) : this system uses functional p53-CFP and Mdm2-YFP fusion proteins and time-lapse fluorescence microscopy. We found that p53 was expressed in a series of discrete pulses after DNA damage. Genetically identical cells had different numbers of pulses: zero, one, two or more. The mean height and duration of each pulse were fixed and did not depend on the amount of DNA damage. The mean number of pulses, however, increased with DNA damage. This approach can be used to study other signaling systems and suggests that the p53-Mdm2 feedback loop generates a digital clock that releases well-timed quanta of p53 until damage is repaired or the cell dies.
引用
收藏
页码:147 / 150
页数:4
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