Institute for Biological Sciences, National Research Council of Canada, Ottawa, Ontario.
J Mol Biol 216: 729-41 (1990)
Abstract
A total of 4051 suboptimal secondary structures are predicted by
folding the 5' non-coding region of ten polioviruses, five human
rhinoviruses and three coxsackieviruses using our new suboptimal folding
algorithm for the prediction of both optimal and suboptimal RNA
secondary structures. A comparative analysis of these RNA secondary
structures reveals the conservation of common secondary structure that
can be supported by phylogenetic data. The thermodynamic stability and
statistical significance of these predicted, conserved helical elements
are assessed and significant structure motifs in the 5' non-coding
region are proposed. The possible roles of these structure motifs in the
virus life cycle are discussed.
Mesh Headings
Unique Identifier: 91080160