Published online 30 March 2005
Article |
Torsional restraint: a new twist on frameshifting pseudoknots
Department of Cell Biology and Molecular Genetics Microbiology Building Room 2135 University of Maryland College Park, MD 20742, USA
*To whom correspondence should be addressed. Tel: +1 301 405 0981; Fax: +1 301 314 9489; Email: dinman{at}umd.edu
Received January 31, 2005. Revised March 9, 2005. Accepted March 9, 2005.
mRNA pseudoknots have a stimulatory function in programmed 1 ribosomal frameshifting (1 PRF). Though we previously presented a model for how mRNA pseudoknots might activate the mechanism for 1 PRF, it did not address the question of the role that they may play in positioning the mRNA relative to the ribosome in this process [E. P. Plant, K. L. M. Jacobs, J. W. Harger, A. Meskauskas, J. L. Jacobs, J. L. Baxter, A. N. Petrov and J. D. Dinman (2003) RNA, 9, 168174]. A separate torsional restraint model suggests that mRNA pseudoknots act to increase the fraction of ribosomes directed to pause with the upstream heptameric slippery site positioned at the ribosome's A- and P-decoding sites [J. D. Dinman (1995) Yeast, 11, 11151127]. Here, experiments using a series of pseudo-pseudoknots having different degrees of rotational freedom were used to test this model. The results of this study support the mechanistic hypothesis that 1 ribosomal frameshifting is enhanced by torsional resistance of the mRNA pseudoknot.
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