TY - JOUR
T1 - Module-based construction of plasmids for chromosomal integration of the fission yeast Schizosaccharomyces pombe
AU - Kakui, Yasutaka
AU - Sunaga, Tomonari
AU - Arai, Kunio
AU - Dodgson, James
AU - Ji, Liang
AU - Csikász-Nagy, Attila
AU - Carazo-Salas, Rafael
AU - Sato, Masamitsu
N1 - Publisher Copyright:
© 2015 The Authors.
PY - 2015/6/24
Y1 - 2015/6/24
N2 - 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 timeconsuming, 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.
AB - 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 timeconsuming, 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.
KW - Chromosomal integration
KW - Cloning
KW - Fission yeast
KW - Fluorescent protein
KW - Plasmid
UR - http://www.scopus.com/inward/record.url?scp=84942474777&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84942474777&partnerID=8YFLogxK
U2 - 10.1098/rsob.150054
DO - 10.1098/rsob.150054
M3 - Article
C2 - 26108218
AN - SCOPUS:84942474777
SN - 2046-2441
VL - 5
JO - Open Biology
JF - Open Biology
IS - 6
M1 - 150054
ER -