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Solution studies of the dimerization initiation site of HIV-1 genomic RNA
Author(s) -
Frédéric Dardel,
Roland Marquet,
Chantal Ehresmann,
Bernard Ehresmann,
Sylvain Blanquet
Publication year - 1998
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/26.15.3567
Subject(s) - rna , intramolecular force , biology , base pair , dimer , oligonucleotide , loop (graph theory) , stem loop , helix (gastropod) , nuclear magnetic resonance spectroscopy , dna , crystallography , biophysics , stereochemistry , biochemistry , gene , chemistry , physics , nuclear magnetic resonance , ecology , mathematics , combinatorics , snail
Dimerization of HIV-1 genomic RNA is an essential step of the viral cycle, initiated at a conserved stem-loop structure which forms a 'kissing complex' involving loop-loop interactions (dimerization initiation site, DIS). A 19mer RNA oligonucleotide (DIS-19) has been synthesized which forms a stable symmetrical dimer in solution at millimolar concentrations. Dimerization does not depend on addition of Mg2+. RNA ligation experiments unambiguously indicate that the formed dimer is a stable kissing complex under the NMR experimental conditions.1H NMR resonance assignments were obtained for DIS-19 at 290 K and pH 6.5. Analysis of the pattern of NOE connectivities reveals that the helix formed by loop-loop base pairing is stacked onto the two terminal stems. Non-canonical base pairs between two essential and conserved adenines are found at the junctions between the two intramolecular and the single intramolecular helices.

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