When chromosomal replication is impeded in the presence of DNA damage, memb
ers of a newly discovered UmuC/DinB/Rev1/Rad30 superfamily of procaryotic a
nd eucaryotic DNA polymerases catalyze translesion synthesis at blocked rep
lication forks. Although these polymerases share sequence elements essentia
lly unrelated to the standard replication and repair enzymes, some of them
(such as the SOS-induced Escherichia coli pol V) catalyze 'error-prone' tra
nslesion synthesis leading to large increases in mutation, whereas others (
an example being the Xeroderma pigmentosum variant gene product XPV pol eta
) carry out aberrant, yet nonmutagenic translesion synthesis. Ongoing studi
es of these low fidelity polymerases could provide new insights into the me
chanism of somatic hypermutation, a key element in the immune response.