Nucleic Acids Research, Vol 25, Issue 14 2690-2693, Copyright © 1997 by Oxford University Press
E Jankowsky, G Strunk and B Schwenzer
Long RNA substrates are inefficiently cleaved by hammerhead ribozymes in
trans. Oligonucleotide facilitators capable of affecting the ribozyme
activity by interacting with the substrates at the termini of the ribozyme
provide a possibility to improve ribozyme mediated cleavage of long RNA
substrates. We have examined the effect of PNA as facilitator in vitro in
order to test if even artificial compounds have facilitating potential.
Effects of 12mer PNA- (peptide nucleic acid), RNA- and DNA-facilitators of
identical sequence were measured with three substrates containing either
942, 452 or 39 nucleotides. The PNA facilitator enhances the ribozyme
activity with both, the 942mer and the 452mer substrate to a slightly
smaller extent than RNA and DNA facilitators. This effect was observed up
to PNA facilitator:substrate ratios of 200:1. The enhancement becomes
smaller as the PNA facilitator:substrate ratio exceeds 200:1. With the
39mer substrate, the PNA facilitator decreases the ribozyme activity by
more than 100- fold, even at PNA facilitator:substrate ratios of 1:1.
Although with long substrates the effect of the PNA facilitator is slightly
smaller than the effect of identical RNA or DNA facilitators, PNA may be a
more practical choice for potential applications in vivo because PNA is
much more resistant to degradation by cellular enzymes.
ARTICLES
Peptide nucleic acid (PNA) is capable of enhancing hammerhead ribozyme activity with long but not with short RNA substrates
Institut fur Biochemie, Technische Universitat Dresden, Mommsenstrasse 13, 01069 Dresden, Germany.
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