Why the study?
How retroviral Gag proteins recognize packaging signals on genomic RNA remains a key unanswered question.
Identifying elements crucial for MPMV gRNA packaging helps understand retrovirus virion assembly and may facilitate the construction of safer retroviral vectors for human gene therapy.
Dual-loop Gag-Psi binding explains MPMV gRNA selectivity; leaves open conservation across retroviruses.
How retroviral Gag proteins recognize the packaging signals (Psi) on their genomic RNA (gRNA) is a key question that we addressed here using Mason-Pfizer monkey virus (MPMV) as a model system by combining band-shift assays and footprinting experiments. Our data show that Pr78Gag selects gRNA against spliced viral RNA by simultaneously binding to two single stranded loops on the MPMV Psi RNA: (1) a large purine loop (ssPurines), and (2) a loop which partially overlaps with a mostly base-paired purine repeat (bpPurines) and extends into a GU-rich binding motif. Importantly, this second Gag binding site is located immediately downstream of the major splice donor (mSD) and is thus absent from the spliced viral RNAs. Identifying elements crucial for MPMV gRNA packaging should help in understanding not only the mechanism of virion assembly by retroviruses, but also facilitate construction of safer retroviral vectors for human gene therapy.
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Pitchai et al. (2021) studied this question.
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