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Originally published In Press as doi:10.1074/jbc.M205295200 on August 22, 2002
J. Biol. Chem., Vol. 277, Issue 45, 43233-43242, November 8, 2002
Direct and Indirect Contributions of RNA Secondary Structure
Elements to the Initiation of HIV-1 Reverse Transcription*
Valérie
Goldschmidt ,
Mickaël
Rigourd ,
Chantal
Ehresmann ,
Stuart F. J.
Le Grice§,
Bernard
Ehresmann , and
Roland
Marquet ¶
From the UPR 9002 du CNRS affiliée à
l'Université Louis Pasteur, Institut de Biologie
Moléculaire et Cellulaire, 15 rue René Descartes, 67084 Strasbourg cedex, France and the § Resistance Mechanisms
Laboratory, NCI-Frederick, National Institutes of Health,
Frederick, Maryland 21702
Initiation of human immunodeficiency virus type 1 (HIV-1) reverse transcription requires specific recognition between the viral RNA (vRNA), tRNA ,
which acts as primer, and reverse transcriptase (RT). The specificity
of this ternary complex is mediated by intricate interactions between the HIV-1 RNA and tRNA . Here, we
compared the relative importance of the secondary structure elements of
this complex in the initiation process. To this aim, we used the
previously published three-dimensional model of the initiation complex
to rationally introduce a series of deletions and substitutions in the
vRNA. When necessary, we used chemical probing to check the structure
of the tRNA -mutant vRNA complexes.
For each of them, we measured the binding affinity of RT and the
kinetics of initial extension of
tRNA and of synthesis of the ( )
strand strong stop DNA. Our results were overall in keeping with the
three-dimensional model of the initiation complex. Surprisingly, we
found that disruption of the intermolecular template-primer
interactions, which are not directly recognized by RT, more severely
affected reverse transcription than deletions or disruption of one of
the intramolecular helices to which RT directly binds. Perturbations of
the highly constrained junction between the intermolecular helix formed
by the primer binding site and the 3' end of
tRNA and the helix immediately
upstream also had dramatic effects on the initiation of reverse
transcription. Taken together, our results demonstrate the overwhelming
importance of the overall three-dimensional structure of the initiation
complex and identify structural elements that constitute promising
targets for anti-initiation-specific drugs.
*
This work was supported by a grant from the Agence Nationale
de la Recherche contre le Sida and a Jeunes Equipes grant from the
CNRS.The costs of publication of this
article were defrayed in part by the
payment of page charges. The article
must therefore be hereby marked
"advertisement" in
accordance with 18 U.S.C. Section
1734 solely to indicate this fact.
¶
To whom correspondence should be addressed. Tel.:
33-3-88-41-70-91; Fax: 33-3-88-60-22-18; E-mail:
r.marquet@ibmc.u-strasbg.fr.
Copyright © 2002 by The American Society for Biochemistry and Molecular Biology, Inc.

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Copyright © 2002 by the American Society for Biochemistry and Molecular Biology.
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