Construction of Mutant Alleles in Saccharomyces cerevisiae without Cloning: Overview and the Delitto Perfetto Method
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Summary
A protocol is provided for the delitto perfetto PCR‐ and oligonucleotide‐based mutagenesis method, which offers particular advantages for generating several different mutant alleles of the same gene.
- Type
- article
- Published
- 2013-10-01
- Cited by
- 12
- References
- 41
- OpenAlex
- https://openalex.org/W1923625669
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:31364025
Keywords
Biology, Genetics, Mutagenesis, Locus (genetics), Saccharomyces cerevisiae
References
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- In vivo site-directed mutagenesis using oligonucleotides
- One-step gene disruption in yeast.
- Targeting, disruption, replacement, and allele rescue: integrative DNA transformation in yeast.
- Site-specific genomic (SSG) and random domain-localized (RDL) mutagenesis in yeast
- The delitto perfetto approach to in vivo site-directed mutagenesis and chromosome rearrangements with synthetic oligonucleotides in yeast.
- A new efficient gene disruption cassette for repeated use in budding yeast
- Site-specific recombination determined by I-SceI, a mitochondrial group I intron-encoded endonuclease expressed in the yeast nucleus.
- Additional modules for versatile and economical PCR‐based gene deletion and modification in Saccharomyces cerevisiae
- New vectors for combinatorial deletions in yeast chromosomes and for gap‐repair cloning using ‘split‐marker’ recombination
- A positive selection for mutants lacking orotidine-5′-phosphate decarboxylase activity in yeast: 5-fluoro-orotic acid resistance
- Replacement of chromosome segments with altered DNA sequences constructed in vitro.
- Direct selection for gene replacement events in yeast.
- Three new dominant drug resistance cassettes for gene disruption in Saccharomyces cerevisiae
- Plasmid-encoded hygromycin B resistance: the sequence of hygromycin B phosphotransferase gene and its expression in Escherichia coli and Saccharomyces cerevisiae.
- Construction of a marker gene cassette which is repeatedly usable for gene disruption in yeast
- Positive and negative selection LYS5MX gene replacement cassettes for use in Saccharomyces cerevisiae
- Heterologous URA3MX cassettes for gene replacement in Saccharomyces cerevisiae
- PCR‐mediated seamless gene deletion and marker recycling in Saccharomyces cerevisiae
Cited by
- The Genomic Landscape of Compensatory Evolution
- Efficient Multiplexed Integration of Synergistic Alleles and Metabolic Pathways in Yeasts via CRISPR-Cas.
- Gene editing for cell engineering: trends and applications
- Simple CRISPR-Cas9 Genome Editing in S. cerevisiae
- Emerging research topics detection with multiple machine learning models
- Opposing functions of the Hda1 complex and histone H2B mono-ubiquitylation in regulating cryptic transcription initiation in Saccharomyces cerevisiae
- Xrn1 is a deNADding Enzyme Modulating Mitochondrial NAD Levels
- Opposing functions of the Hda1 complex and histone H2B mono-ubiquitylation in regulating cryptic transcription in Saccharomyces cerevisiae
- Xrn1 is a deNADding enzyme modulating mitochondrial NAD-capped RNA
- Site-directed mutagenesis of Saccharomyces cerevisiae genome using mismatch PCR product
- Engineering and Evolution of the Complete Reductive Glycine Pathway in Saccharomyces cerevisiae for Formate and CO2 Assimilation
- Yeast Genome Mutagenesis With Multi‐Mismatch PCR: A Rapid and Efficient Strategy for Site‐Directed Mutagenesis in Saccharomyces cerevisiae
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