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Module-based construction of plasmids for chromosomal integration of the fission yeast Schizosaccharomyces pombe
Author(s) -
Yasutaka Kakui,
Tomonari Sunaga,
Kunio Arai,
James Dodgson,
Liang Ji,
Attila CsikászNagy,
Rafael E. CarazoSalas,
Masamitsu Sato
Publication year - 2015
Publication title -
open biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.078
H-Index - 53
ISSN - 2046-2441
DOI - 10.1098/rsob.150054
Subject(s) - plasmid , biology , schizosaccharomyces pombe , genetics , homologous recombination , transformation (genetics) , gene , computational biology , schizosaccharomyces , cloning (programming) , chromosome , saccharomyces cerevisiae , computer science , programming language
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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