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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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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. |
format | Online Article Text |
id | pubmed-5964156 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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