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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...

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Autores principales: Kakui, Yasutaka, Sunaga, Tomonari, Arai, Kunio, Dodgson, James, Ji, Liang, Csikász-Nagy, Attila, Carazo-Salas, Rafael, Sato, Masamitsu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2015
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.
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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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