Nucleic Acids Research Advance Access originally published online on December 18, 2006
Nucleic Acids Research 2007 35(2):614-622; doi:10.1093/nar/gkl1036
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Nucleic Acids Research, 2007, Vol. 35, No. 2 614-622
© 2006 The Author(s).
This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.0/uk/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
RNA |
Encoding folding paths of RNA switches
1 Laboratoire de Dynamique des Fluides Complexes, CNRS-ULP, Institut de Physique 3 rue de l'Université, 67000 Strasbourg, France 2 RNA Dynamics and Biomolecular Systems, Physico-chimie Curie CNRS UMR168, Institut Curie, Section de Recherche, 11 rue P. & M. Curie, 75005 Paris, France
*To whom correspondence should be addressed. Tel: +33 1 42 34 64 74; Email: herve.isambert{at}curie.fr
Received July 17, 2006. Revised November 2, 2006. Accepted November 7, 2006.
RNA co-transcriptional folding has long been suspected to play an active role in helping proper native folding of ribozymes and structured regulatory motifs in mRNA untranslated regions (UTRs). Yet, the underlying mechanisms and coding requirements for efficient co-transcriptional folding remain unclear. Traditional approaches have intrinsic limitations to dissect RNA folding paths, as they rely on sequence mutations or circular permutations that typically perturb both RNA folding paths and equilibrium structures. Here, we show that exploiting sequence symmetries instead of mutations can circumvent this problem by essentially decoupling folding paths from equilibrium structures of designed RNA sequences. Using bistable RNA switches with symmetrical helices conserved under sequence reversal, we demonstrate experimentally that native and transiently formed helices can guide efficient co-transcriptional folding into either long-lived structure of these RNA switches. Their folding path is controlled by the order of helix nucleations and subsequent exchanges during transcription, and may also be redirected by transient antisense interactions. Hence, transient intra- and inter-molecular base pair interactions can effectively regulate the folding of nascent RNA molecules into different native structures, provided limited coding requirements, as discussed from an information theory perspective. This constitutive coupling between RNA synthesis and RNA folding regulation may have enabled the early emergence of autonomous RNA-based regulation networks.
Present addresses: A. Xayaphoummine, Université Paris 7, UMR 7056, 2, place Jussieu, 75251 Paris cedex 05, France
V. Viasnoff, ESPCI, 10 rue Vauquelin, 75005 Paris, France
S. Harlepp, IPCMS–GONLO, 23 rue du Loess BP 43, 67034 Strasbourg cedex 2, France