Abstract
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.
Highlights
Recent advances of genetics and molecular biology of the fission yeast Schizosaccharomyces pombe by researchers have rendered it useful as a model organism to study many aspects of cellular phenomena.In the long history of fission yeast studies, plasmids have been widely used to express external genes
We present a library of plasmids harbouring various modules
We call them ‘module plasmids’, which can be used as entry plasmids for the Golden Gate reaction
Summary
Recent advances of genetics and molecular biology of the fission yeast Schizosaccharomyces pombe by researchers have rendered it useful as a model organism to study many aspects of cellular phenomena. In the long history of fission yeast studies, plasmids have been widely used to express external genes (including epitope-tagged S. pombe genes and genes from external species). Circular plasmids exist as extrachromosomal copies and are not integrated into chromosomes. Plasmid vectors normally contain a marker gene conferring amino acid autotrophy, so that transformants can be selected in selective media (such as EMM and SD) lacking the corresponding amino acid. The effect of expression from plasmids varies in individual cells.
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