A bottom-up approach to gene regulation

被引:252
作者
Guido, NJ
Wang, X
Adalsteinsson, D
McMillen, D
Hasty, J
Cantor, CR
Elston, TC
Collins, JJ
机构
[1] Boston Univ, Ctr Biodynam, Bioinformat Program, Dept Biomed Engn, Boston, MA 02215 USA
[2] Univ N Carolina, Dept Stat & Operat Res, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Dept Math, Chapel Hill, NC 27599 USA
[4] Univ N Carolina, Dept Pharmacol, Chapel Hill, NC 27599 USA
[5] Univ Toronto, Inst Opt Sci, Mississauga, ON L5L 1C6, Canada
[6] Univ Toronto, Dept Chem & Phys Sci, Mississauga, ON L5L 1C6, Canada
[7] Univ Calif San Diego, Dept Bioengn, La Jolla, CA 92093 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
D O I
10.1038/nature04473
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
The ability to construct synthetic gene networks enables experimental investigations of deliberately simplified systems that can be compared to qualitative and quantitative models(1-23). If simple, well-characterized modules can be coupled together into more complex networks with behaviour that can be predicted from that of the individual components, we may begin to build an understanding of cellular regulatory processes from the 'bottom up'. Here we have engineered a promoter to allow simultaneous repression and activation of gene expression in Escherichia coli. We studied its behaviour in synthetic gene networks under increasingly complex conditions: unregulated, repressed, activated, and simultaneously repressed and activated. We develop a stochastic model that quantitatively captures the means and distributions of the expression from the engineered promoter of this modular system, and show that the model can be extended and used to accurately predict the in vivo behaviour of the network when it is expanded to include positive feedback. The model also reveals the counterintuitive prediction that noise in protein expression levels can increase upon arrest of cell growth and division, which we confirm experimentally. This work shows that the properties of regulatory subsystems can be used to predict the behaviour of larger, more complex regulatory networks, and that this bottom-up approach can provide insights into gene regulation.
引用
收藏
页码:856 / 860
页数:5
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