A wealth of experimental data on the mechanism of the picornavirus genome r
eplication has accumulated. Not infrequently, however, conclusions derived
from these data appear to contradict each other. On the one hand, initiatio
n of a complementary RNA strand can be demonstrated to occur in a solution
containing only the poliovirus RNA polymerase, VPg, uridine triphosphate, p
oly(A) template and appropriate ions. On the other hand, convincing experim
ents suggest that efficient initiation of a viral complementary RNA strand
requires complex cis-acting signals on the viral RNA template, additional v
iral and possibly cellular proteins as well as a membrane-containing enviro
nment. On the one hand, there is evidence that the viral RNA, in order to b
e replicated, should first be translated, but on the other hand, the viral
RNA polymerase appears to be unable to overcome the ribosome barrier. Possi
ble solutions for these and several other similar paradoxes are discussed,
along with less contradictory results on the properties of the picornaviral
replicative proteins. Recent results suggesting that recombination and oth
er rearrangements of the viral RNA genomes may be accomplished not only by
the replicative template switching but also by nonreplicative mechanisms ar
e also briefly reviewed. (C) 1999 Elsevier Science B.V. All rights reserved
.