When Poly(A) Binding Proteins Meet Viral Infections, Including SARS-CoV-2

J Virol. 2022 Apr 13;96(7):e0013622. doi: 10.1128/jvi.00136-22. Epub 2022 Mar 16.

Abstract

Viruses have evolved diverse strategies to hijack the cellular gene expression system for their replication. The poly(A) binding proteins (PABPs), a family of critical gene expression factors, are viruses' common targets. PABPs act not only as a translation factor but also as a key factor of mRNA metabolism. During viral infections, the activities of PABPs are manipulated by various viruses, subverting the host translation machinery or evading the cellular antiviral defense mechanism. Viruses harness PABPs by modifying their stability, complex formation with other translation initiation factors, or subcellular localization to promote viral mRNAs translation while shutting off or competing with host protein synthesis. For the past decade, many studies have demonstrated the PABPs' roles during viral infection. This review summarizes a comprehensive perspective of PABPs' roles during viral infection and how viruses evade host antiviral defense through the manipulations of PABPs.

Keywords: host defense; poly(A)-binding protein (PABP); viral infection.

Publication types

  • Review
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antiviral Agents
  • COVID-19*
  • Host Microbial Interactions*
  • Humans
  • Immune Evasion*
  • Poly(A)-Binding Proteins / genetics
  • Poly(A)-Binding Proteins / immunology
  • Protein Biosynthesis
  • RNA, Messenger / metabolism
  • SARS-CoV-2* / genetics
  • SARS-CoV-2* / metabolism

Substances

  • Antiviral Agents
  • Poly(A)-Binding Proteins
  • RNA, Messenger