The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
Directed Evolution of an RNA Enzyme
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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Citations
Cites
Primer-Directed Enzymatic Amplification of DNA with a Thermostable DNA Polymerase
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Cited by
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Chemical etiology of nucleic acid structure
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The RNA World: molecular cooperation at the origins of life
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“It is noteworthy that the main approach to developing ribozymes with desired activities is in vitro selection that, at least conceptually, mimics the Darwinian evolution of ribozymes thought to occur in the primeval RNA world [49,50].”
BackgroundMirror symmetry breaking at the molecular level.
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Lipid-like Self-Assembling Peptides
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Metadata
- Authors
- Beaudry, A. A., & Joyce, G. F.
- Venue
- Science
- Published
- 1992-07-31
- Volume
- 257
- Issue
- 5070
- Pages
- 635-641
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- OpenAlex
- W1973352434
- Cited by
- 447
- References
- 3
- FWCI
- 13.87
- Type
- journal article
- Language
- en
- Open access
- closed
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