Tj. Haggerty et St. Lovett, SUPPRESSION OF RECJ MUTATIONS OF ESCHERICHIA-COLI BY MUTATIONS IN TRANSLATION INITIATION FACTOR-IF3, Journal of bacteriology, 175(19), 1993, pp. 6118-6125
We have isolated genetic suppressors of mutations in the recJ gene of
Escherichia coli in a locus we term srjA. These srjA mutations cause p
artial to complete alleviation of the recombination and UV repair defe
cts conferred by recJ153 and recJ154 mutations in a recBC sbcA genetic
background. The srjA gene was mapped to 37.5 min on the E. coli chrom
osome. This chromosomal region from the srjA5 strain was cloned into a
plasmid vector and was shown to confer recj suppression in a dominant
fashion. Mutational analysis of this plasmid mapped srjA to the infC
gene encoding translation initiation factor 3 (IF3). Sequence analysis
revealed that all three srjA alleles cause amino acid substitutions o
f IF3. Suppression of recj was shown to be allele specific: recJ153 an
d recJ154 mutations were suppressible, but recJ77 and the insertion al
lele recJ284=Tn10 were not. In addition, growth medium-conditional let
hality was observed for strains carrying srjA mutations with the nonsu
ppressible recj alleles. When introduced into recJ+ strains, srjA muta
tions conferred hyperrecombinational and hyper-UV(r) phenotypes. An in
teresting implication of these genetic properties of srjA suppression
is that IF3 may regulate the expression of recj and perhaps other reco
mbination genes and hence may regulate the recombinational capacity of
the cell.