We have developed a procedure, composed of a set of computer programs,
for predicting common RNA structures of homologous sequences. Given a
set of homologous RNAs, these programs perform a multiple sequence al
ignment, generate a list of possible helical stems that are thermodyna
mically favored in RNA folding from a selected individual sequence, es
tablish a conserved stem list by inspecting the equivalent base pairin
gs and/or conserved helical stems from the derived alignment of homolo
gous RNAs, and build common RNA secondary structures with the maximum
scores (i.e., compensatory base changes and number of base pairs, etc.
). The approach is a combination of phylogenetic and thermodynamic met
hods and has been applied to the prediction of common folding structur
es of the 5' untranslated regions in a number of positive RNA viruses.
(C) 1995 Academic Press, Inc.