AB2497 and its mutS and umuDC derivatives were EMS-treated at the stat
ionary phase and specificity of mutation measured. It was found that:
(i) in mutS+ cells EMS induces predominantly GC --> AT transitions (by
supB or supE(oc) formation) and in mutS- cells mainly AT --> TA trans
versions (by supL(NG) formation); (ii) transversions of AT --> TA are
umuDC-dependent and mutational specificity is biased towards AT --> GC
transitions in muts umuDC strains. When mutS-umuDC- cells were transf
ected with plasmids bearing umuD'C or umuDC genes, mutational specific
ity was again biased towards AT --> TA transversions; (iii) experiment
s with bacteria bearing umuC=lacZ or recA=lacZ fusions suggest that pr
ocessing of UmuD --> UmuD' might be poorer in EMS-treated mutS- than i
n mutS' cells.