Studies of the Astrovirus Signal That Induces (−1) Ribosomal Frameshifting
- 1 January 1997
- book chapter
- Published by Springer Nature
- Vol. 412, 323-330
- https://doi.org/10.1007/978-1-4899-1828-4_53
Abstract
Human astroviruses use a (−1) ribosomal frameshift mechanism to regulate expression of the viral RNA-dependent RNA polymerase gene. To evaluate the efficiency of the astrovirus frameshift signal in cell culture, different regions of the frameshift signal were cloned into the rhesus rotavirus VP4 gene and expressed in an infection-transfection transient expression cell culture system. The various astrovirus-VP4 constructs were transfected into BHK-21 cells infected with a recombinant vaccinia virus that expresses T7 RNA polymerase (vTF7—3). All constructs contain a T7 promoter, a picornavirus internal ribosome entry site, and a T7 terminator. Frameshifted and non-frameshifted proteins were distinguished by immunoprecipitation with monoclonal antibodies specific for either the VP4 amino-or carboxy-terminus. Frameshifting efficiency was calculated as the ratio of radioactive counts in the frameshifted protein to the total counts in both the frameshifted and nonframeshifted proteins as determined by Phosphorimager analysis. We found the efficiency of astrovirus frameshifting in intact cells to be 25–28%, significantly greater than the 5–7% efficiency reported previously in a cell-free uncoupled translation system. Since the transfected plasmid is expressed in the cytoplasm in the infection-transfection system, the frameshifting efficiency determined by this assay may be a more accurate reflection of the level of frameshifting for this RNA virus in which transcription and translation are likely coupled in the cytoplasm of infected cells. This hypothesis is supported by the observation that the level of astrovirus frameshifting is increased three-fold when evaluated in a cell-free coupled transcription-translation system. These studies also confirm in intact cells what was previously determined in cell-free studies: the shifty hep-tamer is an absolute requirement for astrovirus ribosomal frameshifting, but deletion of sequences downstream of the stem-loop that are potentially involved in pseudoknot formation does not affect the efficiency of frameshifting.Keywords
This publication has 17 references indexed in Scilit:
- Etiology and outcome of diarrhea after marrow transplantation: A prospective studyGastroenterology, 1994
- New mammalian expression vectorsNature, 1990
- The carboxyl-terminal part of the putative Berne virus polymerase is expressed by ribosomal frameshifting and contains sequence motifs which indicate that toro- and coronaviruses are evolutionary relatedNucleic Acids Research, 1990
- The primary structure and expression of the second open reading frame of the polymerase gene of the coronavirus MHV-A59; a highly conserved polymerase is expressed by an efficient ribosomal frameshifting mechanismNucleic Acids Research, 1990
- Translational Suppression in Gene Expression in Retroviruses and RetrotransposonsPublished by Springer Nature ,1990
- Characterization of an efficient coronavirus ribosomal frameshifting signal: Requirement for an RNA pseudoknotCell, 1989
- HIV expression strategies: Ribosomal frameshifting is directed by a short sequence in both mammalian and yeast systemsCell, 1988
- Expression of the Rous Sarcoma Virus pol Gene by Ribosomal FrameshiftingScience, 1985
- VIRUSES IN INFANTILE GASTROENTERITISPublished by Elsevier ,1975
- VIRUSES AND GASTROENTERITIS IN INFANTSThe Lancet, 1975