TY - JOUR
T1 - Identification of Pr78Gag Binding Sites on the Mason-Pfizer Monkey Virus Genomic RNA Packaging Determinants
AU - Pitchai, Fathima Nuzra Nagoor
AU - Chameettachal, Akhil
AU - Vivet-Boudou, Valérie
AU - Ali, Lizna Mohamed
AU - Pillai, Vineeta N.
AU - Krishnan, Anjana
AU - Bernacchi, Serena
AU - Mustafa, Farah
AU - Marquet, Roland
AU - Rizvi, Tahir A.
N1 - Publisher Copyright:
© 2021 The Author(s)
PY - 2021/5/14
Y1 - 2021/5/14
N2 - 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.
AB - 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.
KW - Footprinting
KW - Gag-RNA interactions
KW - Purines
KW - Retroviruses
KW - hSHAPE
UR - http://www.scopus.com/inward/record.url?scp=85103654682&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85103654682&partnerID=8YFLogxK
U2 - 10.1016/j.jmb.2021.166923
DO - 10.1016/j.jmb.2021.166923
M3 - Article
C2 - 33713677
AN - SCOPUS:85103654682
SN - 0022-2836
VL - 433
JO - Journal of Molecular Biology
JF - Journal of Molecular Biology
IS - 10
M1 - 166923
ER -