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Nucleic Acids Research 2006 34(1):343-352; doi:10.1093/nar/gkj427
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Published online 12 January 2006

© The Author 2006. Published by Oxford University Press. All rights reserved
The online version of this article has been published under an open access model. Users are entitled to use, reproduce, disseminate, or display the open access version of this article for non-commercial purposes provided that: the original authorship is properly and fully attributed; the Journal and Oxford University Press are attributed as the original place of publication with the correct citation details given; if an article is subsequently reproduced or disseminated not in its entirety but only in part or as a derivative work this must be clearly indicated. For commercial re-use, please contact journals.permissions{at}oxfordjournals.org

Article

A new NMR solution structure of the SL1 HIV-1Lai loop–loop dimer

Fabien Kieken, Françoise Paquet, Fabienne Brulé, Jacques Paoletti and Gérard Lancelot*

Centre de Biophysique Moléculaire (Affiliated to the Orléans University), Rue Charles Sadron 45071 Orléans Cedex2, France

*To whom correspondence should be addressed. Tel: +33 2 38 25 55 71; Email: lancelot{at}cnrs-orleans.fr

Received November 25, 2005. Revised December 15, 2005. Accepted December 15, 2005.

Dimerization of genomic RNA is directly related with the event of encapsidation and maturation of the virion. The initiating sequence of the dimerization is a short autocomplementary region in the hairpin loop SL1. We describe here a new solution structure of the RNA dimerization initiation site (DIS) of HIV-1Lai. NMR pulsed field-gradient spin-echo techniques and multidimensional heteronuclear NMR spectroscopy indicate that this structure is formed by two hairpins linked by six Watson–Crick GC base pairs. Hinges between the stems and the loops are stabilized by intra and intermolecular interactions involving the A8, A9 and A16 adenines. The coaxial alignment of the three A-type helices present in the structure is supported by previous crystallography analysis but the A8 and A9 adenines are found in a bulged in position. These data suggest the existence of an equilibrium between bulged in and bulged out conformations in solution.


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