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Published online on July 30, 2002, 10.1073/pnas.162223099
PNAS | August 20, 2002 | vol. 99 | no. 17 | 11133-11138


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Biochemistry
A –1 ribosomal frameshift element that requires base pairing across four kilobases suggests a mechanism of regulating ribosome and replicase traffic on a viral RNA

Jennifer K. Barry *, and W. Allen Miller {dagger}

Plant Pathology Department, Iowa State University, Ames, IA 50011

Edited by Reed B. Wickner, National Institutes of Health, Bethesda, MD, and approved June 14, 2002 (received for review April 12, 2002)

Programmed –1 ribosomal frameshifting is necessary for translation of the polymerase genes of many viruses. In addition to the consensus elements in the mRNA around the frameshift site, we found previously that frameshifting on Barley yellow dwarf virus RNA requires viral sequence located four kilobases downstream. By using dual luciferase reporter constructs, we now show that a predicted loop in the far downstream frameshift element must base pair to a bulge in a bulged stem loop adjacent to the frameshift site. Introduction of either two or six base mismatches in either the bulge or the far downstream loop abolished frameshifting, whereas mutations in both sites that restored base pairing reestablished frameshifting. Likewise, disruption of this base pairing abolished viral RNA replication in plant cells, and restoration of base pairing completely reestablished virus replication. We propose a model in which Barley yellow dwarf virus uses this and another long-distance base-pairing event required for cap-independent translation to allow the replicase copying from the 3' end to shut off translation of upstream ORFs and free the RNA of ribosomes to allow unimpeded replication. This would be a means of solving the "problem," common to positive strand RNA viruses, of competition between ribosomes and replicase for the same RNA template.

Abbreviations: BYDV, Barley yellow dwarf virus; ADSL, adjacent downstream stem loop; LDFE, long-distance frameshift element; WGE, wheat germ extract; UTR, untranslated region; RdRp, RNA-dependent RNA polymerase


* Present address: Pioneer Hi-Bred International, 7300 SW 62nd Avenue, Johnston, IA 50131.

{dagger} To whom reprint requests should be addressed. E-mail: wamiller{at}iastate.edu.

This paper was submitted directly (Track II) to the PNAS office.


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