Dynamically Reshaping Signaling Networks to Program Cell Fate via Genetic Controllers

被引:54
作者
Galloway, Kate E. [1 ]
Franco, Elisa [2 ]
Smolke, Christina D. [3 ]
机构
[1] CALTECH, Div Chem & Chem Engn, Pasadena, CA 91125 USA
[2] Univ Calif Riverside, Dept Mech Engn, Riverside, CA 92521 USA
[3] Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
关键词
MAP KINASE; DIFFERENTIAL REGULATION; CANCER-CELLS; SCAFFOLD; PHOSPHATASE; ROBUSTNESS; YEAST; SPECIFICITY; HOMEOSTASIS; EXPRESSION;
D O I
10.1126/science.1235005
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Engineering of cell fate through synthetic gene circuits requires methods to precisely implement control around native decision-making pathways and offers the potential to direct cell processes. We demonstrate a class of genetic control systems, molecular network diverters, that interface with a native signaling pathway to route cells to divergent fates in response to environmental signals without modification of native genetic material. A method for identifying control points within natural networks is described that enables the construction of synthetic control systems that activate or attenuate native pathways to direct cell fate. We integrate opposing genetic programs by developing network architectures for reduced antagonism and demonstrate rational tuning of performance. Extension of these control strategies to mammalian systems should facilitate the engineering of complex cellular signaling systems.
引用
收藏
页码:1358 / +
页数:12
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