An efficient ribosomal frame-shifting signal in the polymerase-encoding region of the coronavirus IBV.
- 1 December 1987
- journal article
- research article
- Published by Springer Nature in The EMBO Journal
- Vol. 6 (12) , 3779-3785
- https://doi.org/10.1002/j.1460-2075.1987.tb02713.x
Abstract
The polymerase-encoding region of the genomic RNA of the coronavirus infectious bronchitis virus (IBV) contains two very large, briefly overlapping open reading frames (ORF), F1 and F2, and it has been suggested on the basis of sequence analysis that expression of the downstream ORF, F2, might be mediated through ribosomal frame-shifting. To examine this possibility a cDNA fragment containing the F1/F2 overlap region was cloned within a marker gene and placed under the control of the bacteriophage SP6 promoter in a recombinant plasmid. Messenger RNA transcribed from this plasmid, when translated in cell-free systems, specified the synthesis of polypeptides whose size was entirely consistent with the products predicted by an efficient ribosomal frame-shifting event within the overlap region. The nature of the products was confirmed by their reactivity with antisera raised against defined portions of the flanking marker gene. This is the first non-retroviral example of ribosomal frame-shifting in higher eukaryotes.This publication has 39 references indexed in Scilit:
- Studies on transformation of Escherichia coli with plasmidsPublished by Elsevier ,2006
- Translational frameshifting: Where will it stop?Cell, 1987
- Mapping the major transcripts of ground squirrel hepatitis virus: the presumptive template for reverse transcriptase is terminally redundantCell, 1985
- A Leader Sequence is Present on mRNA A of Avian Infectious Bronchitis VirusJournal of General Virology, 1984
- Complete nucleotide sequence of bacteriophage T7 DNA and the locations of T7 genetic elementsJournal of Molecular Biology, 1983
- Frameshift suppressionCell, 1981
- Composition, arrangement and cleavage of the mouse mammary tumor virus polyprotein precursor Pr77gag and p110gagCell, 1979
- A Salmonella frameshift suppressor that acts at runs of a residues in the messenger RNAJournal of Molecular Biology, 1978
- A joint product of the genes gag and pol of Avian Sarcoma Virus: a possible precursor of reverse transcriptaseCell, 1977
- An Efficient mRNA‐Dependent Translation System from Reticulocyte LysatesEuropean Journal of Biochemistry, 1976