The nucleocapsid protein specifically anneals tRNA(Lys-3) onto a noncomplementary primer binding site within the HIV-1 RNA genome in vitro

HIV type 1 (HIV-1) specifically uses host cell tRNA(Lys-3) as a primer for reverse transcription. The 3' 18 nucleotides of this tRNA are complementary to a region on the HIV RNA genome known as the primer binding site (PBS). HIV-1 has a strong preference for maintaining a lysine-specific PBS in vivo, and viral genomes with mutated PBS sequences quickly revert to be complementary tu tRNA(Lys-3). To investigate the mechanism fur thf observed PBS reversion events in vitro, we examined the capability of the nucleocapsid protein (NC) to anneal various tRNA primer sequences onto either complementary or noncomplementary PBSs. We show that NC can anneal different full-length tRNAs onto viral RNA transcripts derived from the HIV-1 MAL or HXB2 isolates, provided that the PBS is complementary to the tRNA used. In contrast, NC promotes specific annealing of only tRNA(Lys-3) onto an RNA template (HXB2) whose PIGS sequence has been mutated to be complementary to the 3' IS nt of human tRNA(Pro). Moreover, HIV-1 reverse transcriptase extends this binary complex from the proline-specific PES. The formation of the noncomplementary binary complex does not occur when a chimeric tRNA(Lys/Pro) containing proline-specific D and anticodon domains is used as the primer, Thus, elements outside the acceptor-T Psi C domains of tRNA(Lys-3) play an important role in preferential primer use in vitro. Our results support the hypothesis that mutant PBS reversion is a result of tRNA(Lys-3) annealing onto end extension from a PBS that specifies an alternate host cell tRNA.