Abstract
An in vitro evolution procedure was used to obtain RNA enzymes with a particular catalytic function. A population of 10 13 variants of the Tetrahymena ribozyme, a group I ribozyme that catalyzes sequence-specific cleavage of RNA via a phosphoester transfer mechanism, was generated. This enzyme has a limited ability to cleave DNA under conditions of high temperature or high MgCl 2 concentration, or both. A selection constraint was imposed on the population of ribozyme variants such that only those individuals that carried out DNA cleavage under physiologic conditions were amplified to produce "progeny" ribozymes. Mutations were introduced during amplification to maintain heterogeneity in the population. This process was repeated for ten successive generations, resulting in enhanced (100 times) DNA cleavage activity.
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Dates
Type | When |
---|---|
Created | 18 years, 10 months ago (Oct. 5, 2006, 7:03 p.m.) |
Deposited | 1 year, 7 months ago (Jan. 10, 2024, 11:07 p.m.) |
Indexed | 3 weeks, 6 days ago (Aug. 2, 2025, 1:15 a.m.) |
Issued | 33 years ago (July 31, 1992) |
Published | 33 years ago (July 31, 1992) |
Published Print | 33 years ago (July 31, 1992) |
@article{Beaudry_1992, title={Directed Evolution of an RNA Enzyme}, volume={257}, ISSN={1095-9203}, url={http://dx.doi.org/10.1126/science.1496376}, DOI={10.1126/science.1496376}, number={5070}, journal={Science}, publisher={American Association for the Advancement of Science (AAAS)}, author={Beaudry, Amber A. and Joyce, Gerald F.}, year={1992}, month=jul, pages={635–641} }