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GeneGenie: optimized oligomer design for directed evolution

GeneGenie, a new online tool available at http://www.gene-genie.org, is introduced to support the design and self-assembly of synthetic genes and constructs. GeneGenie allows for the design of oligonucleotide cohorts encoding the gene sequence optimized for expression in any suitable host through an...

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Detalles Bibliográficos
Autores principales: Swainston, Neil, Currin, Andrew, Day, Philip J., Kell, Douglas B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4086129/
https://www.ncbi.nlm.nih.gov/pubmed/24782527
http://dx.doi.org/10.1093/nar/gku336
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author Swainston, Neil
Currin, Andrew
Day, Philip J.
Kell, Douglas B.
author_facet Swainston, Neil
Currin, Andrew
Day, Philip J.
Kell, Douglas B.
author_sort Swainston, Neil
collection PubMed
description GeneGenie, a new online tool available at http://www.gene-genie.org, is introduced to support the design and self-assembly of synthetic genes and constructs. GeneGenie allows for the design of oligonucleotide cohorts encoding the gene sequence optimized for expression in any suitable host through an intuitive, easy-to-use web interface. The tool ensures consistent oligomer overlapping melting temperatures, minimizes the likelihood of misannealing, optimizes codon usage for expression in a selected host, allows for specification of forward and reverse cloning sequences (for downstream ligation) and also provides support for mutagenesis or directed evolution studies. Directed evolution studies are enabled through the construction of variant libraries via the optional specification of ‘variant codons’, containing mixtures of bases, at any position. For example, specifying the variant codon TNT (where N is any nucleotide) will generate an equimolar mixture of the codons TAT, TCT, TGT and TTT at that position, encoding a mixture of the amino acids Tyr, Ser, Cys and Phe. This facility is demonstrated through the use of GeneGenie to develop and synthesize a library of enhanced green fluorescent protein variants.
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spelling pubmed-40861292014-12-01 GeneGenie: optimized oligomer design for directed evolution Swainston, Neil Currin, Andrew Day, Philip J. Kell, Douglas B. Nucleic Acids Res Article GeneGenie, a new online tool available at http://www.gene-genie.org, is introduced to support the design and self-assembly of synthetic genes and constructs. GeneGenie allows for the design of oligonucleotide cohorts encoding the gene sequence optimized for expression in any suitable host through an intuitive, easy-to-use web interface. The tool ensures consistent oligomer overlapping melting temperatures, minimizes the likelihood of misannealing, optimizes codon usage for expression in a selected host, allows for specification of forward and reverse cloning sequences (for downstream ligation) and also provides support for mutagenesis or directed evolution studies. Directed evolution studies are enabled through the construction of variant libraries via the optional specification of ‘variant codons’, containing mixtures of bases, at any position. For example, specifying the variant codon TNT (where N is any nucleotide) will generate an equimolar mixture of the codons TAT, TCT, TGT and TTT at that position, encoding a mixture of the amino acids Tyr, Ser, Cys and Phe. This facility is demonstrated through the use of GeneGenie to develop and synthesize a library of enhanced green fluorescent protein variants. Oxford University Press 2014-07-01 2014-04-29 /pmc/articles/PMC4086129/ /pubmed/24782527 http://dx.doi.org/10.1093/nar/gku336 Text en © The Author(s) 2014. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Swainston, Neil
Currin, Andrew
Day, Philip J.
Kell, Douglas B.
GeneGenie: optimized oligomer design for directed evolution
title GeneGenie: optimized oligomer design for directed evolution
title_full GeneGenie: optimized oligomer design for directed evolution
title_fullStr GeneGenie: optimized oligomer design for directed evolution
title_full_unstemmed GeneGenie: optimized oligomer design for directed evolution
title_short GeneGenie: optimized oligomer design for directed evolution
title_sort genegenie: optimized oligomer design for directed evolution
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4086129/
https://www.ncbi.nlm.nih.gov/pubmed/24782527
http://dx.doi.org/10.1093/nar/gku336
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