Literature DB >> 7510362

DNA-damaging agents stimulate the formation of directed reciprocal translocations in Saccharomyces cerevisiae.

M Fasullo1, P Dave, R Rothstein.   

Abstract

DNA-damaging agents can stimulate the formation of directed reciprocal translocations in strains of Saccharomyces cerevisiae containing his3 recombinational substrates to generate chromosomal rearrangements. Such agents were compared with those that can stimulate sister-chromatid recombination. We show that chemicals and environmental agents that produce a variety of DNA lesions, including bulky adduct, thymidine dimers, interstrand cross-links, double-strand breaks alkylated bases, can stimulate recombination to yield reciprocal translocations. Of the agents tested, only the alkylating agents methyl methanesulfonate (MMS) and N-methyl-N'-nitro-N-nitrosoguanidine (MNNG), and a bifunctional agent that causes bulky DNA adducts, 4-nitroquinoline-N-oxide (4-NQO), significantly stimulate sister-chromatid recombination in our assay. Factors that contribute to the stimulation of interchromosomal recombination include strain genetic background and ploidy.

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Year:  1994        PMID: 7510362     DOI: 10.1016/0921-8777(94)90076-0

Source DB:  PubMed          Journal:  Mutat Res        ISSN: 0027-5107            Impact factor:   2.433


  16 in total

1.  Double-strand breaks associated with repetitive DNA can reshape the genome.

Authors:  Juan Lucas Argueso; James Westmoreland; Piotr A Mieczkowski; Malgorzata Gawel; Thomas D Petes; Michael A Resnick
Journal:  Proc Natl Acad Sci U S A       Date:  2008-08-13       Impact factor: 11.205

2.  Homologous recombinational repair of double-strand breaks in yeast is enhanced by MAT heterozygosity through yKU-dependent and -independent mechanisms.

Authors:  J A Clikeman; G J Khalsa; S L Barton; J A Nickoloff
Journal:  Genetics       Date:  2001-02       Impact factor: 4.562

3.  The Saccharomyces cerevisiae RAD9 checkpoint reduces the DNA damage-associated stimulation of directed translocations.

Authors:  M Fasullo; T Bennett; P AhChing; J Koudelik
Journal:  Mol Cell Biol       Date:  1998-03       Impact factor: 4.272

4.  Ku-dependent and Ku-independent end-joining pathways lead to chromosomal rearrangements during double-strand break repair in Saccharomyces cerevisiae.

Authors:  Xin Yu; Abram Gabriel
Journal:  Genetics       Date:  2003-03       Impact factor: 4.562

5.  Multiple recombination pathways for sister chromatid exchange in Saccharomyces cerevisiae: role of RAD1 and the RAD52 epistasis group genes.

Authors:  Zheng Dong; Michael Fasullo
Journal:  Nucleic Acids Res       Date:  2003-05-15       Impact factor: 16.971

6.  Mating type regulates the radiation-associated stimulation of reciprocal translocation events in Saccharomyces cerevisiae.

Authors:  M Fasullo; P Dave
Journal:  Mol Gen Genet       Date:  1994-04

7.  Genomic sequence of a mutant strain of Caenorhabditis elegans with an altered recombination pattern.

Authors:  Ann M Rose; Nigel J O'Neil; Mikhail Bilenky; Yaron S Butterfield; Nawar Malhis; Stephane Flibotte; Martin R Jones; Marco Marra; David L Baillie; Steven J M Jones
Journal:  BMC Genomics       Date:  2010-02-23       Impact factor: 3.969

8.  CYP1A1 I462V polymorphism is associated with reduced genotoxicity in yeast despite positive association with increased cancer risk.

Authors:  Julian Freedland; Cinzia Cera; Michael Fasullo
Journal:  Mutat Res       Date:  2017-02-20       Impact factor: 2.433

9.  Activation of aflatoxin B1 by expression of human CYP1A2 polymorphisms in Saccharomyces cerevisiae.

Authors:  Michael Fasullo; Autumn Smith; Patricia Egner; Cinzia Cera
Journal:  Mutat Res Genet Toxicol Environ Mutagen       Date:  2014-01-25       Impact factor: 2.873

10.  Msh2 blocks an alternative mechanism for non-homologous tail removal during single-strand annealing in Saccharomyces cerevisiae.

Authors:  Glenn M Manthey; Nilan Naik; Adam M Bailis
Journal:  PLoS One       Date:  2009-10-16       Impact factor: 3.240

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