A single-input binary counting module based on serine integrase site-specific recombination

被引:8
|
作者
Zhao, Jia [1 ,5 ]
Pokhilko, Alexandra [1 ,6 ]
Ebenhoeh, Oliver [2 ,3 ]
Rosser, Susan J. [4 ]
Colloms, Sean D. [1 ]
机构
[1] Univ Glasgow, Inst Mol Cell & Syst Biol, Bower Bldg, Glasgow G12 8QQ, Lanark, Scotland
[2] Heinrich Heine Univ, Cluster Excellence Plant Sci CEPLAS, Univ Str 1, D-40225 Dusseldorf, Germany
[3] Heinrich Heine Univ, Inst Quantitat & Theoret Biol, Univ Str 1, D-40225 Dusseldorf, Germany
[4] Univ Edinburgh, Sch Biol Sci, SynthSys Synthet & Syst Biol, CH Waddington Bldg,Kings Bldg,Mayfield Rd, Edinburgh EH9 3JD, Midlothian, Scotland
[5] Novo Nordisk China Pharmaceut Co Ltd, Lei Shing Hong Ctr, Guangshunnan Ave, Beijing 100102, Peoples R China
[6] Univ Oxford, John Radcliffe Hosp, MRC Weatherall Inst Mol Med, Oxford OX3 9DS, England
基金
英国生物技术与生命科学研究理事会; 英国工程与自然科学研究理事会;
关键词
PHI-C31; INTEGRASE; ESCHERICHIA-COLI; TIGHT REGULATION; LOGIC; DIRECTIONALITY; REPLICATION; EXPRESSION; NETWORK; PROTEIN; MEMORY;
D O I
10.1093/nar/gkz245
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 device that counts and records the number of events experienced by an individual cell could have many uses in experimental biology and biotechnology. Here, we report a DNA-based 'latch' that switches between two states upon each exposure to a repeated stimulus. The key component of the latch is a DNA segment whose orientation is inverted by the actions of phi C31 integrase and its recombination directionality factor (RDF). Integrase expression is regulated by an external input, while RDF expression is controlled by the state of the latch, such that the orientation of the invertible segment switches efficiently each time the device receives an input pulse. Recombination occurs over a time scale of minutes after initiation of integrase expression. The latch requires a delay circuit, implemented with a transcriptional repressor expressed in only one state, to ensure that each input pulse results in only one inversion of the DNA segment. Development and optimization of the latch in living cells was driven by mathematical modelling of the recombination reactions and gene expression regulated by the switch. We discuss how N latches built with orthogonal site-specific recombination systems could be chained together to form a binary ripple counter that could count to 2N - 1.
引用
收藏
页码:4896 / 4909
页数:14
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