The rolling-circle mechanism of DNA replication is used by small prokaryoti
c genomes, such as single-stranded phages and plasmids. However, phages and
plasmids have adapted the rolling-circle mechanism differently to suit the
ir contrasting biological needs. The phi X174 phage uses a monomeric initia
tor protein catalytically, displays incomplete termination and recycles the
initiator protein, in order to mass-produce phage progeny. By contrast, to
control replication precisely, the pT181 plasmid uses a dimeric initiator
protein stochiometrically, completes termination and inactivates the initia
tor after each replication cycle. The phi X174 phage and the pT181 plasmid
represent paradigmatic adaptations of the rolling-circle mechanism and coul
d provide models for other replicons.