Pj. Sykes et al., Inversion due to intrachromosomal recombination produced by carcinogens ina transgenic mouse model, MUT RES-F M, 427(1), 1999, pp. 1-9
Citations number
29
Categorie Soggetti
Molecular Biology & Genetics
Journal title
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS
Somatic intrachromosomal recombination (SICR) can result in inversions and
deletions in the DNA. pKZ1 mice possess an Escherichia coli (E. coli) lacZ
transgene which is only expressed after a DNA inversion involving the trans
gene occurs. The E. coli P-galactosidase protein can then be detected in fr
ozen tissue sections using a chromogenic substrate. Therefore, pKZ1 mice ca
n be used to detect SICR inversion events in vivo in different tissues. We
have tested the pKZ1 mouse for its potential as a general mutagenesis model
for detecting SICR in spleen in response to carcinogens which have widely
different mechanisms of genotoxicity. Animals were given a single exposure
of carcinogen and spleen cells were examined 3 days later for inversion eve
nts by histochemical staining of tissue sections. Mitomycin C, X-irradiatio
n, etoposide and methylene chloride caused significant induction of inversi
on events in spleen tissue, ranging from 1.6- to 4.2-fold induction with th
e doses used here. This is the first time that inversion events induced by
these carcinogens have been specifically studied in vivo in a mouse model a
nd the findings expand the repertoire of mutation events known to be caused
by these agents. We suggest that the pKZ1 mouse can be used as a general m
utagenesis model for detection of SICR events and is likely to be a useful
model for studying the mechanism of SICR in response to DNA damaging agents
. (C) 1999 Elsevier Science B.V. All rights reserved.