posted on 2024-07-30, 13:07authored byIsabella
T. Whitworth, Sofia Romero, Abena Kissi-Twum, Rachel Knoener, Mark Scalf, Nathan M. Sherer, Lloyd M. Smith
A critical
part of the hepatitis B virus (HBV) life cycle
is the
packaging of the pregenomic RNA (pgRNA) into nucleocapsids. While
this process is known to involve several viral elements, much less
is known about the identities and roles of host proteins in this process.
To better understand the role of host proteins, we isolated pgRNA
and characterized its protein interactome in cells expressing either
packaging-competent or packaging-incompetent HBV genomes. We identified
over 250 host proteins preferentially associated with pgRNA from the
packaging-competent version of the virus. These included proteins
already known to support capsid formation, enhance viral gene expression,
catalyze nucleocapsid dephosphorylation, and bind to the viral genome,
demonstrating the ability of the approach to effectively reveal functionally
significant host–virus interactors. Three of these host proteins,
AURKA, YTHDF2, and ATR, were selected for follow-up analysis. RNA
immunoprecipitation qPCR (RIP-qPCR) confirmed pgRNA-protein association
in cells, and siRNA knockdown of the proteins showed decreased encapsidation
efficiency. This study provides a template for the use of comparative
RNA-protein interactome analysis in conjunction with virus engineering
to reveal functionally significant host–virus interactions.