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Module-based construction of plasmids for chromosomal integration of the fission yeast Schizosaccharomyces pombe
Integration of an external gene into a fission yeast chromosome is useful to investigate the effect of the gene product. An easy way to knock-in a gene construct is use of an integration plasmid, which can be targeted and inserted to a chromosome through homologous recombination. Despite the advanta...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4632507/ https://www.ncbi.nlm.nih.gov/pubmed/26108218 http://dx.doi.org/10.1098/rsob.150054 |
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author | Kakui, Yasutaka Sunaga, Tomonari Arai, Kunio Dodgson, James Ji, Liang Csikász-Nagy, Attila Carazo-Salas, Rafael Sato, Masamitsu |
author_facet | Kakui, Yasutaka Sunaga, Tomonari Arai, Kunio Dodgson, James Ji, Liang Csikász-Nagy, Attila Carazo-Salas, Rafael Sato, Masamitsu |
author_sort | Kakui, Yasutaka |
collection | PubMed |
description | Integration of an external gene into a fission yeast chromosome is useful to investigate the effect of the gene product. An easy way to knock-in a gene construct is use of an integration plasmid, which can be targeted and inserted to a chromosome through homologous recombination. Despite the advantage of integration, construction of integration plasmids is energy- and time-consuming, because there is no systematic library of integration plasmids with various promoters, fluorescent protein tags, terminators and selection markers; therefore, researchers are often forced to make appropriate ones through multiple rounds of cloning procedures. Here, we establish materials and methods to easily construct integration plasmids. We introduce a convenient cloning system based on Golden Gate DNA shuffling, which enables the connection of multiple DNA fragments at once: any kind of promoters and terminators, the gene of interest, in combination with any fluorescent protein tag genes and any selection markers. Each of those DNA fragments, called a ‘module’, can be tandemly ligated in the order we desire in a single reaction, which yields a circular plasmid in a one-step manner. The resulting plasmids can be integrated through standard methods for transformation. Thus, these materials and methods help easy construction of knock-in strains, and this will further increase the value of fission yeast as a model organism. |
format | Online Article Text |
id | pubmed-4632507 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | The Royal Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-46325072015-11-05 Module-based construction of plasmids for chromosomal integration of the fission yeast Schizosaccharomyces pombe Kakui, Yasutaka Sunaga, Tomonari Arai, Kunio Dodgson, James Ji, Liang Csikász-Nagy, Attila Carazo-Salas, Rafael Sato, Masamitsu Open Biol Research Integration of an external gene into a fission yeast chromosome is useful to investigate the effect of the gene product. An easy way to knock-in a gene construct is use of an integration plasmid, which can be targeted and inserted to a chromosome through homologous recombination. Despite the advantage of integration, construction of integration plasmids is energy- and time-consuming, because there is no systematic library of integration plasmids with various promoters, fluorescent protein tags, terminators and selection markers; therefore, researchers are often forced to make appropriate ones through multiple rounds of cloning procedures. Here, we establish materials and methods to easily construct integration plasmids. We introduce a convenient cloning system based on Golden Gate DNA shuffling, which enables the connection of multiple DNA fragments at once: any kind of promoters and terminators, the gene of interest, in combination with any fluorescent protein tag genes and any selection markers. Each of those DNA fragments, called a ‘module’, can be tandemly ligated in the order we desire in a single reaction, which yields a circular plasmid in a one-step manner. The resulting plasmids can be integrated through standard methods for transformation. Thus, these materials and methods help easy construction of knock-in strains, and this will further increase the value of fission yeast as a model organism. The Royal Society 2015-06-24 /pmc/articles/PMC4632507/ /pubmed/26108218 http://dx.doi.org/10.1098/rsob.150054 Text en http://creativecommons.org/licenses/by/4.0/ © 2015 The Authors. Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited. |
spellingShingle | Research Kakui, Yasutaka Sunaga, Tomonari Arai, Kunio Dodgson, James Ji, Liang Csikász-Nagy, Attila Carazo-Salas, Rafael Sato, Masamitsu Module-based construction of plasmids for chromosomal integration of the fission yeast Schizosaccharomyces pombe |
title | Module-based construction of plasmids for chromosomal integration of the fission yeast Schizosaccharomyces pombe |
title_full | Module-based construction of plasmids for chromosomal integration of the fission yeast Schizosaccharomyces pombe |
title_fullStr | Module-based construction of plasmids for chromosomal integration of the fission yeast Schizosaccharomyces pombe |
title_full_unstemmed | Module-based construction of plasmids for chromosomal integration of the fission yeast Schizosaccharomyces pombe |
title_short | Module-based construction of plasmids for chromosomal integration of the fission yeast Schizosaccharomyces pombe |
title_sort | module-based construction of plasmids for chromosomal integration of the fission yeast schizosaccharomyces pombe |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4632507/ https://www.ncbi.nlm.nih.gov/pubmed/26108218 http://dx.doi.org/10.1098/rsob.150054 |
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