Building Enhancers from the Ground Up: A Synthetic Biology Approach

被引:43
作者
Amit, Roee [1 ,3 ]
Garcia, Hernan G. [2 ]
Phillips, Rob [1 ,3 ]
Fraser, Scott E. [1 ,3 ]
机构
[1] CALTECH, Div Biol, Pasadena, CA 91125 USA
[2] CALTECH, Dept Phys, Pasadena, CA 91125 USA
[3] CALTECH, Div Engn & Appl Sci, Pasadena, CA 91125 USA
关键词
TET REPRESSOR; RNA-POLYMERASE; TRANSCRIPTIONAL REGULATION; THERMODYNAMIC ANALYSIS; GENE-REGULATION; TOGGLE SWITCH; IN-VIVO; EXPRESSION; PROMOTER; BINDING;
D O I
10.1016/j.cell.2011.06.024
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
A challenge of the synthetic biology approach is to use our understanding of a system to recreate a biological function with specific properties. We have applied this framework to bacterial enhancers, combining a driver, transcription factor binding sites, and a poised polymerase to create synthetic modular enhancers. Our findings suggest that enhancer-based transcriptional control depends critically and quantitatively on DNA looping, leading to complex regulatory effects when the enhancer cassettes contain additional transcription factor binding sites for TetR, a bacterial transcription factor. We show through a systematic interplay of experiment and thermodynamic modeling that the level of gene expression can be modulated to convert a variable inducer concentration input into discrete or step-like output expression levels. Finally, using a different DNA-binding protein (TraR), we show that the regulatory output is not a particular feature of the specific DNA-binding protein used for the enhancer but a general property of synthetic bacterial enhancers.
引用
收藏
页码:105 / 118
页数:14
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