Carcinogenesis, Vol 19, 69-72, Copyright © 1998 by Oxford University Press
M Kawanishi, T Matsuda, G Sasaki, T Yagi, S Matsui and H Takebe
A spectrum of crotonaldehyde-induced mutations in the supF gene of the
shuttle vector plasmid pMY189 replicated in human fibroblast cells was
examined. Base sequence analysis of 104 plasmids with mutations in the supF
gene revealed that the majority of the mutations were base substitutions
(85%) and the rest were frameshifts (15%). A single base substitution was
most frequently found (47%), while 25% had multiple base substitutions and
interestingly 13% had tandem (adjacent two) base substitutions. Of the base
substitution mutations, 50% were G:C-->T:A transversions and 23% were
G:C-->A:T transitions. The mutations were not distributed randomly but
were located at several hotspots, most of which were G:C base pairs in
5'-AAGG-3' (or 5'-CCTT-3') sequences. Production of propanodeoxyguanosine
adducts may be related to such specificity in the mutation spectrum.
ARTICLES
A spectrum of mutations induced by crotonaldehyde in shuttle vector plasmids propagated in human cells
Department of Radiation Genetics, Graduate School of Medicine, Kyoto University, Japan. kawanishi@eq1.eqc.kyoto-u.ac.jp
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