Comparative study of the effects of heptameric slippery site composition on -1 frameshifting among different eukaryotic systems.
Identifieur interne : 003F46 ( Main/Exploration ); précédent : 003F45; suivant : 003F47Comparative study of the effects of heptameric slippery site composition on -1 frameshifting among different eukaryotic systems.
Auteurs : Ewan P. Plant [États-Unis] ; Jonathan D. DinmanSource :
- RNA (New York, N.Y.) [ 1355-8382 ] ; 2006.
Descripteurs français
- KwdFr :
- MESH :
English descriptors
- KwdEn :
- MESH :
- chemical : Codon, Oligonucleotides.
- genetics : Escherichia coli.
- metabolism : T-Lymphocytes.
- Base Sequence, Cell Line, Frameshifting, Ribosomal, HIV-1, Humans, Mutagenesis, Site-Directed, Plasmids.
Abstract
Studies of programmed -1 ribosomal frameshifting (-1 PRF) have been approached over the past two decades by many different laboratories using a diverse array of virus-derived frameshift signals in translational assay systems derived from a variety of sources. Though it is generally acknowledged that both absolute and relative -1 PRF efficiency can vary in an assay system-dependent manner, no methodical study of this phenomenon has been undertaken. To address this issue, a series of slippery site mutants of the SARS-associated coronavirus frameshift signal were systematically assayed in four different eukaryotic translational systems. HIV-1 promoted frameshifting was also compared between Escherichia coli and a human T-cell line expression systems. The results of these analyses highlight different aspects of each system, suggesting in general that (1) differences can be due to the assay systems themselves; (2) phylogenetic differences in ribosome structure can affect frameshifting efficiency; and (3) care must be taken to employ the closest phylogenetic match between a specific -1 PRF signal and the choice of translational assay system.
DOI: 10.1261/rna.2225206
PubMed: 16497657
Affiliations:
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Le document en format XML
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<term>Mutagenèse dirigée</term>
<term>Oligonucléotides</term>
<term>Plasmides</term>
<term>Séquence nucléotidique</term>
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<front><div type="abstract" xml:lang="en">Studies of programmed -1 ribosomal frameshifting (-1 PRF) have been approached over the past two decades by many different laboratories using a diverse array of virus-derived frameshift signals in translational assay systems derived from a variety of sources. Though it is generally acknowledged that both absolute and relative -1 PRF efficiency can vary in an assay system-dependent manner, no methodical study of this phenomenon has been undertaken. To address this issue, a series of slippery site mutants of the SARS-associated coronavirus frameshift signal were systematically assayed in four different eukaryotic translational systems. HIV-1 promoted frameshifting was also compared between Escherichia coli and a human T-cell line expression systems. The results of these analyses highlight different aspects of each system, suggesting in general that (1) differences can be due to the assay systems themselves; (2) phylogenetic differences in ribosome structure can affect frameshifting efficiency; and (3) care must be taken to employ the closest phylogenetic match between a specific -1 PRF signal and the choice of translational assay system.</div>
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