| Literature DB >> 11073222 |
J Carnes1, L Frolova, S Zinnen, G Drugeon, M Phillippe, J Justesen, A L Haenni, L Leinwand, L L Kisselev, M Yarus.
Abstract
Using selection-amplification, we have isolated RNAs with affinity for translation termination factors eRF1 and eRF1.eRF3 complex. Individual RNAs not only bind, but inhibit eRF1-mediated release of a model nascent chain from eukaryotic ribosomes. There is also significant but weaker inhibition of eRF1-stimulated eRF3 GTPase and eRF3 stimulation of eRF1 release activity. These latter selected RNAs therefore hinder eRF1.eRF3 interactions. Finally, four RNA inhibitors of release suppress a UAG stop codon in mammalian extracts dependent for termination on eRF1 from several metazoan species. These RNAs are therefore new specific inhibitors for the analysis of eukaryotic termination, and potentially a new class of omnipotent termination suppressors with possible therapeutic significance.Entities:
Mesh:
Substances:
Year: 2000 PMID: 11073222 PMCID: PMC1370017 DOI: 10.1017/s1355838200001242
Source DB: PubMed Journal: RNA ISSN: 1355-8382 Impact factor: 4.942