A system of shuttle vectors and yeast host strains designed for efficient manipulation of DNA in Saccharomyces cerevisiae.
Open Access
- 1 May 1989
- journal article
- research article
- Published by Oxford University Press (OUP) in Genetics
- Vol. 122 (1) , 19-27
- https://doi.org/10.1093/genetics/122.1.19
Abstract
A series of yeast shuttle vectors and host strains has been created to allow more efficient manipulation of DNA in Saccharomyces cerevisiae. Transplacement vectors were constructed and used to derive yeast strains containing nonreverting his3, trp1, leu2 and ura3 mutations. A set of YCp and YIp vectors (pRS series) was then made based on the backbone of the multipurpose plasmid pBLUESCRIPT. These pRS vectors are all uniform in structure and differ only in the yeast selectable marker gene used (HIS3, TRP1, LEU2 and URA3). They possess all of the attributes of pBLUESCRIPT and several yeast-specific features as well. Using a pRS vector, one can perform most standard DNA manipulations in the same plasmid that is introduced into yeast.This publication has 30 references indexed in Scilit:
- Functional inactivation of genes by dominant negative mutationsNature, 1987
- GCN4 protein, synthesize in vitro, binds HIS3 regulatory sequences: Implications for general control of amino acid biosynthetic genes in yeastCell, 1985
- Functional selection and analysis of yeast centromeric DNACell, 1985
- A positive selection for mutants lacking orotidine-5′-phosphate decarboxylase activity in yeast: 5-fluoro-orotic acid resistanceMolecular Genetics and Genomics, 1984
- DNA sequences of yeast H3 and H4 histone genes from two non-allelic gene sets encode identical H3 and H4 proteinsJournal of Molecular Biology, 1983
- [12] One-step gene disruption in yeastPublished by Elsevier ,1983
- Nucleotide sequence of yeast LEU2 shows 5′-noncoding region has sequences cognate to leucineCell, 1982
- Centromeric DNA from Saccharomyces cerevisiaeJournal of Molecular Biology, 1982
- Deletion analysis of the Saccharomyces GAL gene cluster: Transcription from three promotersJournal of Molecular Biology, 1981
- Screening λgt Recombinant Clones by Hybridization to Single Plaques in SituScience, 1977