The enzymology of RNase YI, a recently discovered endoribonuclease fr
om yeast, was studied and compared to other endonucleases for detectio
n of single-strand regions and base pair mismatches in RNA. Its value
for RNA structure analyses was assessed with Escherichia coli 5S rRNA
as a model substrate. The generally accepted structure of the 5S rRNA
is based on thermodynamic energy considerations as well as structures
conserved in regions of the molecule during evolution. S1 and mung bea
n nucleases gave similar results with very marked preference only for
the longest single-stranded region in the model. RNase YI was much mo
re discriminating for detecting unpaired nucleotides as well as short
single-strand regions and predicted the generally accepted 5S rRNA str
ucture. Preliminary experiments also indicated that RNase YI was more
sensitive than RNase I for detecting single or multiple base pair mis
matches in an RNA-DNA hybrid.