Nucleic Acids Research, Vol 25, Issue 2 333-338, Copyright © 1997 by Oxford University Press
M Sioud
The efficacy of intracellular binding of hammerhead ribozyme to its
cleavage site in target RNA is a major requirement for its use as a
therapeutic agent. Such efficacy can be influenced by several factors, such
as the length of the ribozyme antisense arms and mRNA secondary structures.
Analysis of various IL-2 hammerhead ribozymes having different antisense
arms but directed to the same site predicts that the hammerhead ribozyme
target site is present within a double-stranded region that is flanked by
single-stranded loops. Extension of the low cleaving hammerhead ribozyme
antisense arms by nucleotides that base pair with the single-stranded
regions facilitated the hammerhead ribozyme binding to longer RNA
substrates (e.g. mRNA). In addition, a correlation between the in vitro and
intracellular results was also found. Thus, the present study would
facilitate the design of hammerhead ribozymes directed against higher order
structured sites. Further, it emphasises the importance of detailed
structural investigations of hammerhead ribozyme full-length target RNAs.
ARTICLES
Effects of variations in length of hammerhead ribozyme antisense arms upon the cleavage of longer RNA substrates
Institute of Immunology and Rheumatology, The National Hospital, Fr. Qvamsgt. 1, N-0172 Oslo, Norway. mosioud@embnet.uio.no
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