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. 1991 Apr 11;19(7):1577-83.
doi: 10.1093/nar/19.7.1577.

Characterization of HIV-1 REV protein: binding stoichiometry and minimal RNA substrate

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Free PMC article

Characterization of HIV-1 REV protein: binding stoichiometry and minimal RNA substrate

K S Cook et al. Nucleic Acids Res. .
Free PMC article

Abstract

The HIV-1 REV protein binds to the stem II region of the REV-responsive element (RNA). Studies to further define the RNA sequence and structure specifically bound by REV protein identify a minimal RNA element of 40 nucleotides. Analysis of RNA fragments by gel retardation and filter binding suggest that a core element composed of one particular stem with flanking sequences capable of forming a second double stranded region is essential for specific recognition by REV protein. Stable REV-RNA complexes are formed in a stoichiometry of 1 REV: 1 RNA. The minimal RNA element binds 1 REV molecule while the stem II saturates at 3 REV molecules per RNA. These results establish that REV recognizes a primary binding site within the RRE and support the notion that the initial viral transcript binding event involves a monomeric REV protein.

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References

    1. Nucleic Acids Res. 1981 Jan 10;9(1):133-48 - PubMed
    1. J Mol Biol. 1968 Jul 14;34(2):365-8 - PubMed
    1. Science. 1988 Feb 19;239(4842):910-3 - PubMed
    1. J Bacteriol. 1988 Mar;170(3):1245-53 - PubMed
    1. Proc Natl Acad Sci U S A. 1988 Apr;85(7):2071-5 - PubMed

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