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L-SCRaMbLE as a tool for light-controlled Cre-mediated recombination in yeast

The synthetic yeast genome constructed by the International Synthetic Yeast Sc2.0 consortium adds thousands of loxPsym recombination sites to all 16 redesigned chromosomes, allowing the shuffling of Sc2.0 chromosome parts by the Cre-loxP recombination system thereby enabling genome evolution experim...

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Autores principales: Hochrein, Lena, Mitchell, Leslie A., Schulz, Karina, Messerschmidt, Katrin, Mueller-Roeber, Bernd
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5964156/
https://www.ncbi.nlm.nih.gov/pubmed/29789561
http://dx.doi.org/10.1038/s41467-017-02208-6
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author Hochrein, Lena
Mitchell, Leslie A.
Schulz, Karina
Messerschmidt, Katrin
Mueller-Roeber, Bernd
author_facet Hochrein, Lena
Mitchell, Leslie A.
Schulz, Karina
Messerschmidt, Katrin
Mueller-Roeber, Bernd
author_sort Hochrein, Lena
collection PubMed
description The synthetic yeast genome constructed by the International Synthetic Yeast Sc2.0 consortium adds thousands of loxPsym recombination sites to all 16 redesigned chromosomes, allowing the shuffling of Sc2.0 chromosome parts by the Cre-loxP recombination system thereby enabling genome evolution experiments. Here, we present L-SCRaMbLE, a light-controlled Cre recombinase for use in the yeast Saccharomyces cerevisiae. L-SCRaMbLE allows tight regulation of recombinase activity with up to 179-fold induction upon exposure to red light. The extent of recombination depends on induction time and concentration of the chromophore phycocyanobilin (PCB), which can be easily adjusted. The tool presented here provides improved recombination control over the previously reported estradiol-dependent SCRaMbLE induction system, mediating a larger variety of possible recombination events in SCRaMbLE-ing a reporter plasmid. Thereby, L-SCRaMbLE boosts the potential for further customization and provides a facile application for use in the S. cerevisiae genome re-engineering project Sc2.0 or in other recombination-based systems.
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spelling pubmed-59641562018-05-24 L-SCRaMbLE as a tool for light-controlled Cre-mediated recombination in yeast Hochrein, Lena Mitchell, Leslie A. Schulz, Karina Messerschmidt, Katrin Mueller-Roeber, Bernd Nat Commun Article The synthetic yeast genome constructed by the International Synthetic Yeast Sc2.0 consortium adds thousands of loxPsym recombination sites to all 16 redesigned chromosomes, allowing the shuffling of Sc2.0 chromosome parts by the Cre-loxP recombination system thereby enabling genome evolution experiments. Here, we present L-SCRaMbLE, a light-controlled Cre recombinase for use in the yeast Saccharomyces cerevisiae. L-SCRaMbLE allows tight regulation of recombinase activity with up to 179-fold induction upon exposure to red light. The extent of recombination depends on induction time and concentration of the chromophore phycocyanobilin (PCB), which can be easily adjusted. The tool presented here provides improved recombination control over the previously reported estradiol-dependent SCRaMbLE induction system, mediating a larger variety of possible recombination events in SCRaMbLE-ing a reporter plasmid. Thereby, L-SCRaMbLE boosts the potential for further customization and provides a facile application for use in the S. cerevisiae genome re-engineering project Sc2.0 or in other recombination-based systems. Nature Publishing Group UK 2018-05-22 /pmc/articles/PMC5964156/ /pubmed/29789561 http://dx.doi.org/10.1038/s41467-017-02208-6 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Hochrein, Lena
Mitchell, Leslie A.
Schulz, Karina
Messerschmidt, Katrin
Mueller-Roeber, Bernd
L-SCRaMbLE as a tool for light-controlled Cre-mediated recombination in yeast
title L-SCRaMbLE as a tool for light-controlled Cre-mediated recombination in yeast
title_full L-SCRaMbLE as a tool for light-controlled Cre-mediated recombination in yeast
title_fullStr L-SCRaMbLE as a tool for light-controlled Cre-mediated recombination in yeast
title_full_unstemmed L-SCRaMbLE as a tool for light-controlled Cre-mediated recombination in yeast
title_short L-SCRaMbLE as a tool for light-controlled Cre-mediated recombination in yeast
title_sort l-scramble as a tool for light-controlled cre-mediated recombination in yeast
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5964156/
https://www.ncbi.nlm.nih.gov/pubmed/29789561
http://dx.doi.org/10.1038/s41467-017-02208-6
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