Rotavirus variant replicates efficiently although encoding an aberrant NSP3 that fails to induce nuclear localization of poly(A)-binding protein

J Gen Virol. 2012 Jul;93(Pt 7):1483-1494. doi: 10.1099/vir.0.041830-0. Epub 2012 Mar 21.

Abstract

The rotavirus (RV) non-structural protein NSP3 forms a dimer that has binding domains for the translation initiation factor eIF4G and for a conserved 3'-terminal sequence of viral mRNAs. Through these activities, NSP3 has been proposed to promote viral mRNA translation by directing circularization of viral polysomes. In addition, by disrupting interactions between eIF4G and the poly(A)-binding protein (PABP), NSP3 has been suggested to inhibit translation of host polyadenylated mRNAs and to stimulate relocalization of PABP from the cytoplasm to the nucleus. Herein, we report the isolation and characterization of SA11-4Fg7re, an SA11-4F RV derivative that contains a large sequence duplication initiating within the genome segment (gene 7) encoding NSP3. Our analysis showed that mutant NSP3 (NSP3m) encoded by SA11-4Fg7re is almost twice the size of the wild-type protein and retains the capacity to dimerize. However, in comparison to wild-type NSP3, NSP3m has a decreased capacity to interact with eIF4G and to suppress the translation of polyadenylated mRNAs. In addition, NSP3m fails to induce the nuclear accumulation of PABP in infected cells. Despite the defective activities of NSP3m, the levels of viral protein and progeny virus produced in SA11-4Fg7re- and SA11-4F-infected cells were indistinguishable. Collectively, these data are consistent with a role for NSP3 in suppressing host protein synthesis through antagonism of PABP activity, but also suggest that NSP3 functions may have little or no impact on the efficiency of virus replication in widely used RV-permissive cell lines.

Publication types

  • Research Support, N.I.H., Intramural

MeSH terms

  • Animals
  • Eukaryotic Initiation Factor-4G / metabolism
  • Guinea Pigs
  • Molecular Sequence Data
  • Mutant Proteins / genetics
  • Mutant Proteins / metabolism
  • Poly(A)-Binding Proteins / metabolism*
  • Protein Binding
  • Protein Multimerization
  • Protein Transport
  • RNA, Viral / genetics
  • Repetitive Sequences, Nucleic Acid
  • Rotavirus / genetics
  • Rotavirus / physiology*
  • Sequence Analysis, DNA
  • Viral Nonstructural Proteins / genetics*
  • Viral Nonstructural Proteins / metabolism*
  • Virus Replication*

Substances

  • Eukaryotic Initiation Factor-4G
  • Mutant Proteins
  • NSP3 protein, Rotavirus
  • Poly(A)-Binding Proteins
  • RNA, Viral
  • Viral Nonstructural Proteins

Associated data

  • GENBANK/GU550506