Literature DB >> 8244029

Multiple tandem integrations of transforming DNA sequences in yeast chromosomes suggest a mechanism for integrative transformation by homologous recombination.

A Plessis1, B Dujon.   

Abstract

In yeast, the fate of linear DNA molecules upon transformation is determined by the existence of sequence homology between chromosomes and the ends of the transforming molecule. To understand the mechanism of integration of transforming DNA, we have studied the influence of DNA concentration on the frequency and type of transformants obtained, using either non-replicative or replicative plasmids. In both cases, increasing DNA concentration results in multiple tandem repeats integrated into the chromosome containing the homologous target sequence. When a diploid strain is transformed, multiple tandem repeats occur in only one of the two homologous chromosomes at a time. The frequency distribution of the different types of integrants observed indicates non-independent integration events likely to result from plasmid-plasmid interaction prior to chromosome integration. In addition, our results define the proper conditions for optimized gene targetting or gene rescue experiments.

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Year:  1993        PMID: 8244029     DOI: 10.1016/0378-1119(93)90172-y

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  14 in total

1.  Targeted DNA integration within different functional gene domains in yeast reveals ORF sequences as recombinational cold-spots.

Authors:  K Gjuracic; E Pivetta; C V Bruschi
Journal:  Mol Genet Genomics       Date:  2004-03-27       Impact factor: 3.291

2.  Expansions and contractions in a tandem repeat induced by double-strand break repair.

Authors:  F Pâques; W Y Leung; J E Haber
Journal:  Mol Cell Biol       Date:  1998-04       Impact factor: 4.272

3.  A eubacterial gene conferring spectinomycin resistance on Chlamydomonas reinhardtii: integration into the nuclear genome and gene expression.

Authors:  H Cerutti; A M Johnson; N W Gillham; J E Boynton
Journal:  Genetics       Date:  1997-01       Impact factor: 4.562

4.  RAD51 is required for the repair of plasmid double-stranded DNA gaps from either plasmid or chromosomal templates.

Authors:  S Bärtsch; L E Kang; L S Symington
Journal:  Mol Cell Biol       Date:  2000-02       Impact factor: 4.272

Review 5.  Multiple pathways of recombination induced by double-strand breaks in Saccharomyces cerevisiae.

Authors:  F Pâques; J E Haber
Journal:  Microbiol Mol Biol Rev       Date:  1999-06       Impact factor: 11.056

Review 6.  Chromosomal editing in Escherichia coli. Vectors for DNA integration and excision.

Authors:  P Balbás; G Gosset
Journal:  Mol Biotechnol       Date:  2001-09       Impact factor: 2.695

Review 7.  Role of RAD52 epistasis group genes in homologous recombination and double-strand break repair.

Authors:  Lorraine S Symington
Journal:  Microbiol Mol Biol Rev       Date:  2002-12       Impact factor: 11.056

8.  Recombinational repair of gaps in DNA is asymmetric in Ustilago maydis and can be explained by a migrating D-loop model.

Authors:  D O Ferguson; W K Holloman
Journal:  Proc Natl Acad Sci U S A       Date:  1996-05-28       Impact factor: 11.205

9.  Single strand and double strand DNA damage-induced reciprocal recombination in yeast. Dependence on nucleotide excision repair and RAD1 recombination.

Authors:  W A Saffran; R B Greenberg; M S Thaler-Scheer; M M Jones
Journal:  Nucleic Acids Res       Date:  1994-07-25       Impact factor: 16.971

10.  The DNA damage checkpoint pathways exert multiple controls on the efficiency and outcome of the repair of a double-stranded DNA gap.

Authors:  Edwin Haghnazari; Wolf-Dietrich Heyer
Journal:  Nucleic Acids Res       Date:  2004-08-10       Impact factor: 16.971

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