Synthetic in vitro transcriptional oscillators

被引:237
作者
Kim, Jongmin [1 ]
Winfree, Erik [2 ,3 ,4 ]
机构
[1] CALTECH, Dept Biol, Pasadena, CA 91125 USA
[2] CALTECH, Dept Comp Sci, Pasadena, CA 91125 USA
[3] CALTECH, Dept Computat & Neural Syst, Pasadena, CA 91125 USA
[4] CALTECH, Dept Bioengn, Pasadena, CA 91125 USA
基金
美国国家科学基金会;
关键词
cell free; in vitro; oscillation; synthetic biology; transcriptional circuits; CELL-CYCLE OSCILLATOR; FEEDBACK; NETWORK; DESIGN; SYSTEM; ROBUST; PRINCIPLES; PREDATOR; RHYTHMS; MODELS;
D O I
10.1038/msb.2010.119
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The construction of synthetic biochemical circuits from simple components illuminates how complex behaviors can arise in chemistry and builds a foundation for future biological technologies. A simplified analog of genetic regulatory networks, in vitro transcriptional circuits, provides a modular platform for the systematic construction of arbitrary circuits and requires only two essential enzymes, bacteriophage T7 RNA polymerase and Escherichia coli ribonuclease H, to produce and degrade RNA signals. In this study, we design and experimentally demonstrate three transcriptional oscillators in vitro. First, a negative feedback oscillator comprising two switches, regulated by excitatory and inhibitory RNA signals, showed up to five complete cycles. To demonstrate modularity and to explore the design space further, a positive-feedback loop was added that modulates and extends the oscillatory regime. Finally, a three-switch ring oscillator was constructed and analyzed. Mathematical modeling guided the design process, identified experimental conditions likely to yield oscillations, and explained the system's robust response to interference by short degradation products. Synthetic transcriptional oscillators could prove valuable for systematic exploration of biochemical circuit design principles and for controlling nanoscale devices and orchestrating processes within artificial cells. Molecular Systems Biology 7: 465; published online 1 February 2011; doi: 10.1038/msb.2010.119
引用
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页数:15
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