Selection of guide sequences that direct efficient cleavage of mRNA by human ribonuclease P - PubMed (original) (raw)
. 1994 Mar 4;263(5151):1269-73.
doi: 10.1126/science.8122108.
Affiliations
- PMID: 8122108
- DOI: 10.1126/science.8122108
Selection of guide sequences that direct efficient cleavage of mRNA by human ribonuclease P
Y Yuan et al. Science. 1994.
Abstract
Any RNA, when in a complex with another oligoribonucleotide known as an external guide sequence (EGS), can become a substrate for ribonuclease P. Simulation of evolution in vitro was used to select EGSs that bind tightly to a target substrate messenger RNA and that increase the efficiency of cleavage of the target by human ribonuclease P to a level equal to that achieved with natural substrates. The most efficient EGSs form transfer RNA precursor-like structures with the target RNA, in which the analog of the anticodon stem has been disrupted, an indication that selection for the optimal substrate for ribonuclease P yields an RNA structure different from that of present-day transfer RNA precursors.
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