| Literature DB >> 29626221 |
Inga Soreanu1, Adi Hendler1, Danielle Dahan1, Daniel Dovrat1, Amir Aharoni2.
Abstract
The budding yeast is currently one of the major model organisms for the study of a wide variety of biological processes. Genetic manipulation of yeast involves the extensive usage of selectable markers that can lead to undesired effects. Thus, marker-free genetic manipulation in yeast is highly desirable for gene/promoter replacement and various other applications. Here we combine the power of selectable markers followed by CRISPR/CAS9 genome editing for common genetic manipulations in yeast in a marker-free manner. We demonstrate our approach for whole gene and promoter replacements and for high-efficiency operator array integration. Our approach allows the utilization of many thousands of existing strains including library strains for the generation of significant genetic changes in yeast in a marker-free and cloning-free fashion.Entities:
Keywords: CRISPR/CAS9; Marker-free; S. cerevisiae; Yeast
Mesh:
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Year: 2018 PMID: 29626221 DOI: 10.1007/s00294-018-0831-y
Source DB: PubMed Journal: Curr Genet ISSN: 0172-8083 Impact factor: 3.886