Structural basis for the specificity of the initiation of HIV-1 reverse transcription

Initiation of human immunodeficiency virus type I (HIV-1) reverse transcription requires specific recognition of the viral genome, tRNA(3)(Lys), which acts as primer, and reverse transcriptase (RT), The specificity of this ternary complex is mediated by intricate interactions between HIV-1 RNA and tRNA(3)(Lys), hot remains poorly understood at the three-dimensional level, We used chemical probing to gain insight into the three-dimensional structure of the viral RNA-tRNA(3)(Lys) complex, and enzymatic footprinting to delineate regions interacting with RT, These and previous experimental data were used to derive a three-dimensional model of the initiation complex. The viral RNA and tRNA(3)(Lys) form a compact structure in which the two RNAs fold into distinct structural domains. The extended interactions between these molecules are not directly recognized by RT, Rather, they favor RT binding by preventing steric clashes between the nucleic acids and the polymerase and inducing a viral RNA-tRNA(3)(Lys) conformation which fits perfectly into the nucleic acid binding cleft of RT, Recognition of the 3' end of tRNA(3)(Lys) and of the first template nucleotides by RT is favored by a kink in the template strand promoted by the short junctions present in the previously established secondary structure.