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Journal of Virology, January 2000, p. 264-271, Vol. 74, No. 1
Leiden Institute of Chemistry, Leiden
University, 2300 RA Leiden, The Netherlands
Received 30 December 1998/Accepted 29 September 1999
Recently, we showed that the main determinant in the tRNA-like
structure of turnip yellow mosaic virus RNA to initiate minus-strand synthesis in vitro is the 3' ACCA end. By mutational analysis of the
3'-terminal hairpin, we show here that only a non-base-paired ACCA end
is functional and that the stability of the wild-type 3'-proximal
hairpin is the most favorable, in that it has the lowest
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Copyright © 2000, American Society for Microbiology. All rights reserved.
In Vitro Transcription by the Turnip Yellow Mosaic
Virus RNA Polymerase: a Comparison with the Alfalfa Mosaic Virus and
Brome Mosaic Virus Replicases
G value and a high transcription efficiency. With a
nested set of RNA fragments, we show that the minimum template length is 9 nucleotides and that transcription is improved with increasing the
length of the template. The results also suggest that proper base
stacking contributes to efficient transcription initiation. Internal
initiation is shown to take place on every NPyCPu sequence of a
nonstructured template. However, the position of the internal initiation site in the template is important, and competition between
the different sites takes place. Internal initiation was also studied
with the RNA-dependent RNA polymerase of brome mosaic virus (BMV) and
alfalfa mosaic virus (AlMV). The BMV polymerase can start internally on
ACCA sequences, though inefficiently. Unexpectedly, the polymerases of
both AlMV and BMV can start efficiently on an internal AUGC sequence.
*
Corresponding author. Mailing address: Leiden Institute
of Chemistry, Leiden University, P.O. Box 9502, 2300 RA Leiden, The Netherlands. Phone: (31)715274769. Fax: (31)715274340. E-mail: c.pley{at}chem.leidenuniv.nl.
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