Hostname: page-component-cd9895bd7-p9bg8 Total loading time: 0 Render date: 2024-12-24T12:34:41.165Z Has data issue: false hasContentIssue false

Programmed +1 frameshifting stimulated by complementarity between a downstream mRNA sequence and an error-correcting region of rRNA

Published online by Cambridge University Press:  07 February 2001

ZIRONG LI
Affiliation:
Department of Biological Sciences and Program in Molecular and Cell Biology, University of Maryland, Baltimore County, Baltimore, Maryland 21250, USA
GUILLAUME STAHL
Affiliation:
Department of Biological Sciences and Program in Molecular and Cell Biology, University of Maryland, Baltimore County, Baltimore, Maryland 21250, USA
PHILIP J. FARABAUGH
Affiliation:
Department of Biological Sciences and Program in Molecular and Cell Biology, University of Maryland, Baltimore County, Baltimore, Maryland 21250, USA
Get access

Abstract

Like most retroviruses and retrotransposons, the retrotransposon Ty3 expresses its pol gene analog (POL3) as a translational fusion to the upstream gag analog (GAG3). The Gag3-Pol3 fusion occurs by frameshifting during translation of the mRNA that encodes the two separate but overlapping ORFs. We showed previously that the shift occurs by out-of-frame binding of a normal aminoacyl-tRNA in the ribosomal A site caused by an aberrant codon[bull ]anticodon interaction in the P site. This event is unlike all previously described programmed translational frameshifts because it does not require tRNA slippage between cognate or near-cognate codons in the mRNA. A sequence of 15 nt distal to the frameshift site stimulates frameshifting 7.5-fold. Here we show that the Ty3 stimulator acts as an unstructured region to stimulate frameshifting. Its function depends on strict spacing from the site of frameshifting. Finally, the stimulator increases frameshifting dependent on sense codon-induced pausing, but has no effect on frameshifting dependent on pauses induced by nonsense codons. Complementarity between the stimulator and a portion of the accuracy center of the ribosome, Helix 18, implies that the stimulator may directly disrupt error correction by the ribosome.

Type
Research Article
Copyright
2001 RNA Society

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)