TY - JOUR
T1 - Defining Distinct RNA-Protein Interactomes of SARS-CoV-2 Genomic and Subgenomic RNAs
AU - Whitworth, Isabella T.
AU - Knoener, Rachel A.
AU - Puray-Chavez, Maritza
AU - Halfmann, Peter
AU - Romero, Sofia
AU - Baddouh, M’bark
AU - Scalf, Mark
AU - Kawaoka, Yoshihiro
AU - Kutluay, Sebla B.
AU - Smith, Lloyd M.
AU - Sherer, Nathan M.
N1 - Publisher Copyright:
© 2023 American Chemical Society.
PY - 2024/1/5
Y1 - 2024/1/5
N2 - Host RNA binding proteins recognize viral RNA and play key roles in virus replication and antiviral mechanisms. SARS-CoV-2 generates a series of tiered subgenomic RNAs (sgRNAs), each encoding distinct viral protein(s) that regulate different aspects of viral replication. Here, for the first time, we demonstrate the successful isolation of SARS-CoV-2 genomic RNA and three distinct sgRNAs (N, S, and ORF8) from a single population of infected cells and characterize their protein interactomes. Over 500 protein interactors (including 260 previously unknown) were identified as associated with one or more target RNA. These included protein interactors unique to a single RNA pool and others present in multiple pools, highlighting our ability to discriminate between distinct viral RNA interactomes despite high sequence similarity. Individual interactomes indicated viral associations with cell response pathways, including regulation of cytoplasmic ribonucleoprotein granules and posttranscriptional gene silencing. We tested the significance of three protein interactors in these pathways (APOBEC3F, PPP1CC, and MSI2) using siRNA knockdowns, with several knockdowns affecting viral gene expression, most consistently PPP1CC. This study describes a new technology for high-resolution studies of SARS-CoV-2 RNA regulation and reveals a wealth of new viral RNA-associated host factors of potential functional significance to infection.
AB - Host RNA binding proteins recognize viral RNA and play key roles in virus replication and antiviral mechanisms. SARS-CoV-2 generates a series of tiered subgenomic RNAs (sgRNAs), each encoding distinct viral protein(s) that regulate different aspects of viral replication. Here, for the first time, we demonstrate the successful isolation of SARS-CoV-2 genomic RNA and three distinct sgRNAs (N, S, and ORF8) from a single population of infected cells and characterize their protein interactomes. Over 500 protein interactors (including 260 previously unknown) were identified as associated with one or more target RNA. These included protein interactors unique to a single RNA pool and others present in multiple pools, highlighting our ability to discriminate between distinct viral RNA interactomes despite high sequence similarity. Individual interactomes indicated viral associations with cell response pathways, including regulation of cytoplasmic ribonucleoprotein granules and posttranscriptional gene silencing. We tested the significance of three protein interactors in these pathways (APOBEC3F, PPP1CC, and MSI2) using siRNA knockdowns, with several knockdowns affecting viral gene expression, most consistently PPP1CC. This study describes a new technology for high-resolution studies of SARS-CoV-2 RNA regulation and reveals a wealth of new viral RNA-associated host factors of potential functional significance to infection.
KW - RNA binding proteins
KW - RNA-protein interactions
KW - SARS-CoV-2
KW - coronaviruses
KW - host−pathogen interactions
KW - subgenomic RNA
KW - viral proteomics
UR - http://www.scopus.com/inward/record.url?scp=85180084183&partnerID=8YFLogxK
U2 - 10.1021/acs.jproteome.3c00506
DO - 10.1021/acs.jproteome.3c00506
M3 - Article
C2 - 38043095
AN - SCOPUS:85180084183
SN - 1535-3893
VL - 23
SP - 149
EP - 160
JO - Journal of Proteome Research
JF - Journal of Proteome Research
IS - 1
ER -