The secondary structures of human hY1 and hY5 RNAs were determined usi
ng both chemical modification techniques and enzymatic structure probi
ng. The results indicate that both for hY1 and for hY5 RNA the seconda
ry structure largely corresponds to the structure predicted by sequenc
e alignment and computerized energy-minimization. However, some import
ant deviations were observed. In the case of hY1 RNA, two regions form
ing a predicted helix appeared to be single-stranded. Furthermore, the
pyrimidine-rich region of hY1 RNA appeared to be very resistant to re
agents under native conditions, although it was accessible to chemical
reagents under semi-denaturing conditions. This may point to yet unid
entified tertiary interactions for this region of hY1 RNA. In the case
of hY5 RNA, two neighbouring internal loops in the predicted structur
e appeared to form one large internal loop.