Diversity-based, model-guided construction of synthetic gene networks with predicted functions

被引:350
作者
Ellis, Tom [1 ,2 ,3 ]
Wang, Xiao [1 ,2 ,3 ]
Collins, James J. [1 ,2 ,3 ]
机构
[1] Boston Univ, Howard Hughes Med Inst, Boston, MA 02215 USA
[2] Boston Univ, Dept Biomed Engn, Ctr BioDynam, Boston, MA 02215 USA
[3] Boston Univ, Ctr Adv Biotechnol, Boston, MA 02215 USA
基金
美国国家科学基金会; 美国国家卫生研究院; 英国工程与自然科学研究理事会;
关键词
SACCHAROMYCES-CEREVISIAE; MAMMALIAN-CELLS; ESCHERICHIA-COLI; FEEDFORWARD LOOP; EXPRESSION; PROMOTER; CIRCUIT; YEAST; SWITCH; BACTERIOPHAGE;
D O I
10.1038/nbt.1536
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Engineering artificial gene networks from modular components is a major goal of synthetic biology. However, the construction of gene networks with predictable functions remains hampered by a lack of suitable components and the fact that assembled networks often require extensive, iterative retrofitting to work as intended. Here we present an approach that couples libraries of diversified components ( synthesized with randomized nonessential sequence) with in silico modeling to guide predictable gene network construction without the need for post hoc tweaking. We demonstrate our approach in Saccharomyces cerevisiae by synthesizing regulatory promoter libraries and using them to construct feed-forward loop networks with different predicted input-output characteristics. We then expand our method to produce a synthetic gene network acting as a predictable timer, modifiable by component choice. We use this network to control the timing of yeast sedimentation, illustrating how the plug-and-play nature of our design can be readily applied to biotechnology.
引用
收藏
页码:465 / 471
页数:7
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