Rapid construction of insulated genetic circuits via synthetic sequence-guided isothermal assembly

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Rapid construction of insulated genetic circuits via synthetic sequence-guided isothermal assembly

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Title: Rapid construction of insulated genetic circuits via synthetic sequence-guided isothermal assembly
Author: Torella, Joseph P.; Boehm, Christian R.; Lienert, Florian; Chen, Jan-Hung; Way, Jeffrey C.; Silver, Pamela A.

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Citation: Torella, Joseph P., Christian R. Boehm, Florian Lienert, Jan-Hung Chen, Jeffrey C. Way, and Pamela A. Silver. 2013. “Rapid construction of insulated genetic circuits via synthetic sequence-guided isothermal assembly.” Nucleic Acids Research 42 (1): 681-689. doi:10.1093/nar/gkt860. http://dx.doi.org/10.1093/nar/gkt860.
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Abstract: In vitro recombination methods have enabled one-step construction of large DNA sequences from multiple parts. Although synthetic biological circuits can in principle be assembled in the same fashion, they typically contain repeated sequence elements such as standard promoters and terminators that interfere with homologous recombination. Here we use a computational approach to design synthetic, biologically inactive unique nucleotide sequences (UNSes) that facilitate accurate ordered assembly. Importantly, our designed UNSes make it possible to assemble parts with repeated terminator and insulator sequences, and thereby create insulated functional genetic circuits in bacteria and mammalian cells. Using UNS-guided assembly to construct repeating promoter-gene-terminator parts, we systematically varied gene expression to optimize production of a deoxychromoviridans biosynthetic pathway in Escherichia coli. We then used this system to construct complex eukaryotic AND-logic gates for genomic integration into embryonic stem cells. Construction was performed by using a standardized series of UNS-bearing BioBrick-compatible vectors, which enable modular assembly and facilitate reuse of individual parts. UNS-guided isothermal assembly is broadly applicable to the construction and optimization of genetic circuits and particularly those requiring tight insulation, such as complex biosynthetic pathways, sensors, counters and logic gates.
Published Version: doi:10.1093/nar/gkt860
Other Sources: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3874176/pdf/
Terms of Use: This article is made available under the terms and conditions applicable to Other Posted Material, as set forth at http://nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of-use#LAA
Citable link to this page: http://nrs.harvard.edu/urn-3:HUL.InstRepos:11879201
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