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Translation of polioviral mRNA is inhibited by cleavage of polypyrimidine tract-binding proteins executed by polioviral 3Cpro

  • Sung Hoon Back
  • , Yoon Ki Kim
  • , Woo Jae Kim
  • , Sungchan Cho
  • , Hoe Rang Oh
  • , Jung Eun Kim
  • , Sung Key Jang*
  • *Corresponding author for this work
  • Pohang University of Science and Technology

Research output: Contribution to journalArticlepeer-review

Abstract

The translation of polioviral mRNA occurs through an internal ribosomal entry site (IRES). Several RNA-binding proteins, such as polypyrimidine tract-binding protein (PTB) and poly(rC)-binding protein (PCBP), are required for the poliovirus IRES-dependent translation. Here we report that a poliovirus protein, 3Cpro (and/or 3CDpro), cleaves PTB isoforms (PTB1, PTB2, and PTB4). Three 3Cpro target sites (one major target site and two minor target sites) exist in PTBs. PTB fragments generated by poliovirus infection are redistributed to the cytoplasm from the nucleus, where most of the intact PTBs are localized. Moreover, these PTB fragments inhibit polioviral IRES-dependent translation in a cell-based assay system. We speculate that the proteolytic cleavage of PTBs may contribute to the molecular switching from translation to replication of polioviral RNA.

Original languageEnglish
Pages (from-to)2529-2542
Number of pages14
JournalJournal of Virology
Volume76
Issue number5
DOIs
StatePublished - 2002
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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