Rapidly Characterizing the Fast Dynamics of RNA Genetic Circuitry with Cell-Free Transcription–Translation (TX-TL) Systems

RNA regulators are emerging as powerful tools to engineer synthetic genetic networks or rewire existing ones. A potential strength of RNA networks is that they may be able to propagate signals on time scales that are set by the fast degradation rates of RNAs. However, a current bottleneck to verifying this potential is the slow design-build-test cycle of evaluating these networks in vivo. Here, we adapt an Escherichia coli-based cell-free transcription-translation (TX-TL) system for rapidly prototyping RNA networks. We used this system to measure the response time of an RNA transcription cascade to be approximately five minutes per step of the cascade. We also show that this response time can be adjusted with temperature and regulator threshold tuning. Finally, we use TX-TL to prototype a new RNA network, an RNA single input module, and show that this network temporally stages the expression of two genes in vivo.

[1]  E Westhof,et al.  Progression of a loop–loop complex to a four‐way junction is crucial for the activity of a regulatory antisense RNA , 2000, The EMBO journal.

[2]  E. Wagner,et al.  Antisense RNA‐mediated transcriptional attenuation: an in vitro study of plasmid pT181 , 2000, Molecular microbiology.

[3]  Jeffrey J. Tabor,et al.  Characterizing bacterial gene circuit dynamics with optically programmed gene expression signals , 2014, Nature Methods.

[4]  Adam P Arkin,et al.  An adaptor from translational to transcriptional control enables predictable assembly of complex regulation , 2012, Nature Methods.

[5]  Richard M. Murray,et al.  Resource usage and gene circuit performance characterization in a cell-free ‘breadboard’ , 2013, bioRxiv.

[6]  Christopher A. Voigt,et al.  A Synthetic Genetic Edge Detection Program , 2009, Cell.

[7]  Farren J. Isaacs,et al.  Engineered riboregulators enable post-transcriptional control of gene expression , 2004, Nature Biotechnology.

[8]  Christopher A. Voigt,et al.  Genetic programs constructed from layered logic gates in single cells , 2012, Nature.

[9]  Henrike Niederholtmeyer,et al.  Implementation of cell-free biological networks at steady state , 2013, Proceedings of the National Academy of Sciences.

[10]  J. Kornblum,et al.  pT181 plasmid replication is regulated by a countertranscript-driven transcriptional attenuator , 1989, Cell.

[11]  M. Win,et al.  A modular and extensible RNA-based gene-regulatory platform for engineering cellular function , 2007, Proceedings of the National Academy of Sciences.

[12]  A. J. Carpousis The RNA degradosome of Escherichia coli: an mRNA-degrading machine assembled on RNase E. , 2007, Annual review of microbiology.

[13]  R. Weiss,et al.  A universal RNAi-based logic evaluator that operates in mammalian cells , 2007, Nature Biotechnology.

[14]  J. Stelling,et al.  A tunable synthetic mammalian oscillator , 2009, Nature.

[15]  Peter R Breggin The second wave. , 1973, Mental hygiene.

[16]  Kyle E. Watters,et al.  The centrality of RNA for engineering gene expression , 2013, Biotechnology journal.

[17]  C. Wilson,et al.  Laser-mediated, site-specific inactivation of RNA transcripts. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[18]  Priscilla E. M. Purnick,et al.  The second wave of synthetic biology: from modules to systems , 2009, Nature Reviews Molecular Cell Biology.

[19]  M. Elowitz,et al.  A synthetic oscillatory network of transcriptional regulators , 2000, Nature.

[20]  Richard M. Murray,et al.  Protocols for Implementing an Escherichia coli Based TX-TL Cell-Free Expression System for Synthetic Biology , 2013, Journal of visualized experiments : JoVE.

[21]  Takuya Ueda,et al.  Cell-free translation reconstituted with purified components , 2001, Nature Biotechnology.

[22]  Paul S. Freemont,et al.  Validation of an entirely in vitro approach for rapid prototyping of DNA regulatory elements for synthetic biology , 2013, Nucleic acids research.

[23]  Vincent Noireaux,et al.  Linear DNA for rapid prototyping of synthetic biological circuits in an Escherichia coli based TX-TL cell-free system. , 2014, ACS synthetic biology.

[24]  T. Terwilliger,et al.  Engineering and characterization of a superfolder green fluorescent protein , 2006, Nature Biotechnology.

[25]  Julius B. Lucks,et al.  A modular strategy for engineering orthogonal chimeric RNA transcription regulators , 2013, Nucleic acids research.

[26]  M. Bennett,et al.  A fast, robust, and tunable synthetic gene oscillator , 2008, Nature.

[27]  Uri Alon,et al.  Response delays and the structure of transcription networks. , 2003, Journal of molecular biology.

[28]  David K. Karig,et al.  Expression optimization and synthetic gene networks in cell-free systems , 2011, Nucleic acids research.

[29]  S. Shen-Orr,et al.  Network motifs in the transcriptional regulation network of Escherichia coli , 2002, Nature Genetics.

[30]  J. Keasling,et al.  Library of Synthetic 5′ Secondary Structures To Manipulate mRNA Stability in Escherichia coli , 1999, Biotechnology progress.

[31]  J. Collins,et al.  Construction of a genetic toggle switch in Escherichia coli , 2000, Nature.

[32]  Craig R. Taylor,et al.  The Second Wave. , 2002 .

[33]  Adam P Arkin,et al.  Supplementary information for Rationally designed families of orthogonal RNA regulators of translation , 2012 .

[34]  Markus Wieland,et al.  Programmable single-cell mammalian biocomputers , 2012, Nature.

[35]  Luke A. Gilbert,et al.  Repurposing CRISPR as an RNA-Guided Platform for Sequence-Specific Control of Gene Expression , 2013, Cell.

[36]  David R. Liu,et al.  In vivo evolution of an RNA-based transcriptional activator. , 2003, Chemistry & biology.

[37]  R. Weiss,et al.  Cancer Cells Multi-Input RNAi-Based Logic Circuit for Identification of Specific , 2011 .

[38]  Vincent Noireaux,et al.  Efficient cell-free expression with the endogenous E. Coli RNA polymerase and sigma factor 70 , 2010, Journal of biological engineering.

[39]  Travis S. Bayer,et al.  Programmable ligand-controlled riboregulators of eukaryotic gene expression , 2005, Nature Biotechnology.

[40]  R. Weiss,et al.  Ultrasensitivity and noise propagation in a synthetic transcriptional cascade. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[41]  R. Tsien,et al.  A monomeric red fluorescent protein , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[42]  V. Noireaux,et al.  An E. coli cell-free expression toolbox: application to synthetic gene circuits and artificial cells. , 2012, ACS synthetic biology.

[43]  E. Gerhart H. Wagner,et al.  An Antisense RNA-Mediated Transcriptional Attenuation Mechanism Functions in Escherichia coli , 2002, Journal of bacteriology.

[44]  Cole Trapnell,et al.  Multiplexed RNA structure characterization with selective 2′-hydroxyl acylation analyzed by primer extension sequencing (SHAPE-Seq) , 2011, Proceedings of the National Academy of Sciences.

[45]  Adam P Arkin,et al.  Versatile RNA-sensing transcriptional regulators for engineering genetic networks , 2011, Proceedings of the National Academy of Sciences.

[46]  U. Alon,et al.  Just-in-time transcription program in metabolic pathways , 2004, Nature Genetics.

[47]  R. Bar-Ziv,et al.  Principles of cell-free genetic circuit assembly , 2003, Proceedings of the National Academy of Sciences of the United States of America.

[48]  Julius B. Lucks,et al.  Engineering naturally occurring trans-acting non-coding RNAs to sense molecular signals , 2012, Nucleic acids research.

[49]  M. Jewett,et al.  Cell-free synthetic biology: thinking outside the cell. , 2012, Metabolic engineering.

[50]  S. Basu,et al.  A synthetic multicellular system for programmed pattern formation , 2005, Nature.

[51]  Carola Engler,et al.  A One Pot, One Step, Precision Cloning Method with High Throughput Capability , 2008, PloS one.

[52]  A. Nicholson Function, mechanism and regulation of bacterial ribonucleases. , 1999, FEMS microbiology reviews.