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Functional expression of the cre-lox site-specific recombination system in the yeast Saccharomyces cerevisiae
Open accessAbstract
The procaryotic cre-lox site-specific recombination system of coliphage P1 was shown to function in an efficient manner in a eucaryote, the yeast Saccharomyces cerevisiae. The cre gene, which codes for a site-specific recombinase, was placed under control of the yeast GALI promoter. lox sites flanking the LEU2 gene were integrated into two different chromosomes in both orientations. Excisive recombination at the lox sites (as measured by loss of the LEU2 gene) was promoted efficiently and accurately by the Cre protein and was dependent upon induction by galactose. These results demonstrate that a procaryotic recombinase can enter a eucaryotic nucleus and, moreover, that the ability of the Cre recombinase to perform precise recombination events on the chromosomes of S. cerevisiae is unimpaired by chromatin structure.
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Metadata
- Authors
- Sauer, B.
- Affiliations
- DuPont (United States) (US)
- Corresponding author
- Sauer, B
- Venue
- Molecular and Cellular Biology
- Publisher
- Informa UK Limited
- Published
- 1987-06
- Volume
- 7
- Issue
- 6
- Pages
- 2087-2096
- ISSN
- 0270-7306 (ISSN-L)
- 1098-5549
- PMC
- PMC365329
- OpenAlex
- W1913334531
- Cited by
- 482
- References
- 38
- Citations by year
- 2025: 11 · 2024: 9 · 2023: 15 · 2022: 17 · 2021: 17 · 2020: 15 · 2019: 20 · 2018: 27 · 2017: 15 · 2016: 19 · 2015: 21 · 2014: 34 · 2013: 18 · 2012: 21
- FWCI
- 1.79
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Molecular and Cellular Biology (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Fungal and yeast genetics research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › CRISPR and Genetic Engineering
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › DNA Repair Mechanisms
- Keywords
- Cre recombinase, Saccharomyces cerevisiae, bacteriophage P1, excision, LEU2 gene, GAL1 promoter, galactose induction, chromatin structure, chromosomal integration
- MeSH terms
- Coliphages, DNA Nucleotidyltransferases, DNA Restriction Enzymes, Escherichia coli, Genes, Genes, Fungal, Genes, Viral, Plasmids, Promoter Regions, Genetic, Recombination, Genetic, Saccharomyces cerevisiae, Viral Proteins, Integrases
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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