Literature DB >> 10529734

Background mutations and polymorphisms in lacZ-plasmid transgenic mice.

M E Dollé1, W K Snyder, N J van Orsouw, J Vijg.   

Abstract

Transgenic animal models harboring chromosomally integrated shuttle vectors with bacterial reporter genes are now widely used to measure in vivo mutant frequencies. The lacZ-plasmid transgenic mouse model has a unique sensitivity to large rearrangements compared to systems using bacteriophage lambda vectors, which mainly detect point mutations and small deletions or insertions. In this study, the background mutant frequencies and spectra in the lacZ-plasmid transgenic mouse model were investigated. While the majority of the recovered lacZ-mutants appeared to have originated in the mouse, a subset of mutants are likely to represent artifacts, and occur with a frequency of about 1.3 x 10(-5), irrespective of the total mutant frequency. Galactose-insensitive host cells, due to galE back mutations or galK or galT forward mutations, grow through the positive selection system and cause a small subset of the background. When using HindIII to excise the plasmids from genomic DNA, the largest contribution to the background, (1.1 +/- 0.3) x 10(-5), appeared to be caused by star activity, i.e., cleavage at nucleotide sequences other than the HindIII restriction enzyme recognition sequence, during the recovery procedure. Finally, a total of 10 polymorphic sites in different copies of the lacZ-plasmid cluster in founder line 60 were discovered. Copyright 1999 Wiley-Liss, Inc.

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Year:  1999        PMID: 10529734

Source DB:  PubMed          Journal:  Environ Mol Mutagen        ISSN: 0893-6692            Impact factor:   3.216


  8 in total

1.  Distinct spectra of somatic mutations accumulated with age in mouse heart and small intestine.

Authors:  M E Dollé; W K Snyder; J A Gossen; P H Lohman; J Vijg
Journal:  Proc Natl Acad Sci U S A       Date:  2000-07-18       Impact factor: 11.205

2.  Mutational fingerprints of aging.

Authors:  Martijn E T Dollé; Wendy K Snyder; David B Dunson; Jan Vijg
Journal:  Nucleic Acids Res       Date:  2002-01-15       Impact factor: 16.971

3.  Genome dynamics in aging mice.

Authors:  Martijn E T Dollé; Jan Vijg
Journal:  Genome Res       Date:  2002-11       Impact factor: 9.043

4.  Disruption of Brca2 increases the spontaneous mutation rate in vivo: synergism with ionizing radiation.

Authors:  Andrew N J Tutt; Conny Th M van Oostrom; Gillian M Ross; Harry van Steeg; Alan Ashworth
Journal:  EMBO Rep       Date:  2002-02-15       Impact factor: 8.807

5.  Deficiency of the DNA repair protein nibrin increases the basal but not the radiation induced mutation frequency in vivo.

Authors:  Petra Wessendorf; Jan Vijg; André Nussenzweig; Martin Digweed
Journal:  Mutat Res       Date:  2014-07-11       Impact factor: 2.433

6.  Effect of Ames dwarfism and caloric restriction on spontaneous DNA mutation frequency in different mouse tissues.

Authors:  Ana Maria Garcia; Rita A Busuttil; R Brent Calder; Martijn E T Dollé; Vivian Diaz; C Alex McMahan; Andrzej Bartke; James Nelson; Robert Reddick; Jan Vijg
Journal:  Mech Ageing Dev       Date:  2008-05-13       Impact factor: 5.432

7.  p53 signaling in response to increased DNA damage sensitizes AML1-ETO cells to stress-induced death.

Authors:  Ondrej Krejci; Mark Wunderlich; Hartmut Geiger; Fu-Sheng Chou; David Schleimer; Michael Jansen; Paul R Andreassen; James C Mulloy
Journal:  Blood       Date:  2007-11-01       Impact factor: 22.113

8.  Intra-organ variation in age-related mutation accumulation in the mouse.

Authors:  Rita A Busuttil; Ana Maria Garcia; Robert L Reddick; Martijn E T Dollé; Robert B Calder; James F Nelson; Jan Vijg
Journal:  PLoS One       Date:  2007-09-12       Impact factor: 3.240

  8 in total

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