A bottom-up approach to gene regulation

被引:0
作者
Nicholas J. Guido
Xiao Wang
David Adalsteinsson
David McMillen
Jeff Hasty
Charles R. Cantor
Timothy C. Elston
J. J. Collins
机构
[1] Boston University,Department of Biomedical Engineering, Bioinformatics Program, Center for BioDynamics and Center for Advanced Biotechnology
[2] Department of Statistics and Operations Research,Department of Pharmacology
[3] Department of Mathematics,Institute for Optical Sciences and Department of Chemical and Physical Sciences
[4] University of North Carolina,Department of Bioengineering
[5] University of Toronto at Mississauga,undefined
[6] University of California,undefined
来源
Nature | 2006年 / 439卷
关键词
D O I
暂无
中图分类号
学科分类号
摘要
The ability to construct synthetic gene networks enables experimental investigations of deliberately simplified systems that can be compared to qualitative and quantitative models1,2,3,4,5,6,7,8,9,10,11,12,13,14,15,16,17,18,19,20,21,22,23. 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:4
相关论文
共 78 条
[1]  
Elowitz MB(2000)A synthetic oscillatory network of transcriptional regulators Nature 403 335-338
[2]  
Leibler S(2000)Construction of a genetic toggle switch in Nature 403 339-342
[3]  
Gardner TS(2000)Engineering stability in gene networks by autoregulation Nature 405 590-593
[4]  
Cantor CR(2001)Positive feedback in eukaryotic gene networks: cell differentiation by graded to binary response conversion EMBO J. 20 2528-2535
[5]  
Collins JJ(2002)Stochastic gene expression in a single cell Science 297 1183-1186
[6]  
Becskei A(2002)Regulation of noise in the expression of a single gene Nature Genet. 31 69-73
[7]  
Serrano L(2002)Negative autoregulation speeds the response times of transcription networks J. Mol. Biol. 323 785-793
[8]  
Becskei A(2002)Combinatorial synthesis of genetic networks Science 296 1407-1470
[9]  
Séraphin B(2003)Prediction and measurement of an autoregulatory genetic module Proc. Natl. Acad. Sci. USA 100 7714-7719
[10]  
Serrano L(2003)Noise in eukaryotic gene expression Nature 422 633-637