Literature DB >> 35792909

Insertion orientation within the cassette affects gene-targeting success during ends-out recombination in the yeast Saccharomyces cerevisiae.

Petar Tomev Mitrikeski1,2.   

Abstract

Gene-targeting is one of the most important molecular tools for genomic manipulations for research and industrial purposes. However, many factors influence targeting fidelity undermining the efforts for accurate, fast, and reliable construction of genetically modified yeast strains. Therefore, it is of great academic interest that we uncover as many as possible parameters affecting the recombination mechanisms that enable targeting. Since usually, researchers choose the orientation of the insertion (marker) within the module at random, it seemed interesting to see whether the same module will achieve essentially the same targeting efficiency when the same marker was oriented alternatively concerning the same target gene. Thus, two loci (URA3 and LEU2) and one allele (ura3-52) in a haploid yeast genetic background were targeted by artificial modules bearing homologous insertions in alternative orientations being flanked by long asymmetrical targeting homology to either replace or disrupt a genomic target. Results showed that insertion orientation within the targeting module strongly influences targeting in yeast, regardless of the targeting approach.
© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Entities:  

Keywords:  Ends-out recombination; Gene targeting; Insertion orientation; One-step gene disruption; Transcription; Yeast Saccharomyces cerevisiae

Year:  2022        PMID: 35792909     DOI: 10.1007/s00294-022-01246-y

Source DB:  PubMed          Journal:  Curr Genet        ISSN: 0172-8083            Impact factor:   3.886


  42 in total

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Authors:  F R Cross
Journal:  Yeast       Date:  1997-06-15       Impact factor: 3.239

Review 2.  Transcription and recombination: when RNA meets DNA.

Authors:  Andrés Aguilera; Hélène Gaillard
Journal:  Cold Spring Harb Perspect Biol       Date:  2014-08-01       Impact factor: 10.005

3.  Exploring redundancy in the yeast genome: an improved strategy for use of the cre-loxP system.

Authors:  D Delneri; G C Tomlin; J L Wixon; A Hutter; M Sefton; E J Louis; S G Oliver
Journal:  Gene       Date:  2000-07-11       Impact factor: 3.688

4.  Nucleotide excision repair gene function in short-sequence recombination.

Authors:  A M Bailis; S Maines
Journal:  J Bacteriol       Date:  1996-04       Impact factor: 3.490

5.  A simple and efficient method for direct gene deletion in Saccharomyces cerevisiae.

Authors:  A Baudin; O Ozier-Kalogeropoulos; A Denouel; F Lacroute; C Cullin
Journal:  Nucleic Acids Res       Date:  1993-07-11       Impact factor: 16.971

6.  Suitability of replacement markers for functional analysis studies in Saccharomyces cerevisiae.

Authors:  F Baganz; A Hayes; D Marren; D C Gardner; S G Oliver
Journal:  Yeast       Date:  1997-12       Impact factor: 3.239

7.  Plasmids pEMBLY: new single-stranded shuttle vectors for the recovery and analysis of yeast DNA sequences.

Authors:  C Baldari; G Cesareni
Journal:  Gene       Date:  1985       Impact factor: 3.688

8.  Promoter-dependent disruption of genes: simple, rapid, and specific PCR-based method with application to three different yeast.

Authors:  Thomas D Edlind; Karl W Henry; John-Paul Vermitsky; Merritt P Edlind; Shriya Raj; Santosh K Katiyar
Journal:  Curr Genet       Date:  2005-09-14       Impact factor: 3.886

9.  Precise gene disruption in Saccharomyces cerevisiae by double fusion polymerase chain reaction.

Authors:  D C Amberg; D Botstein; E M Beasley
Journal:  Yeast       Date:  1995-10       Impact factor: 3.239

10.  Ends-in vs. ends-out targeted insertion mutagenesis in Saccharomyces castellii.

Authors:  Eimantas Astromskas; Marita Cohn
Journal:  Curr Genet       Date:  2009-05-13       Impact factor: 3.886

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