Retronphage phi R73 exhibits extensive sequence homology to the satell
ite bacteriophage P4. Bacteriophage P4 superinfection immunity is elic
ited by a small RNA (CI RNA) that causes premature transcription termi
nation within the operon coding for the P4 replication functions. This
control is exerted via interaction of the CI RNA with two complementa
ry target sites on the untranslated leader RNA of the replication oper
on. We found that phi R73 is endowed with a similar immunity system bu
t is heteroimmune to P4. The heteroimmunity is due to six base differe
nces in the CI RNA and to compensatory base substitutions in the targe
t sequences. The sequence differences in the CI RNA are all located in
single-stranded regions, which appear to play a predominant role in t
he interaction with the target sites. Analysis of phage carrying a hyb
rid immunity system indicates that, although two target sequences are
required for the establishment of lysogeny, a single site is sufficien
t to make a phage sensitive to the prophage immunity. (C) 1996 Academi
c Press, Inc.