Varied Movement Strategies Employed by Triple Gene Block-Encoding Viruses

Jeanmarie Verchot-Lubicz, Lesley Torrance, Andrey G. Solovyev, Sergey Yu Morozov, Andrew O. Jackson, David Gilmer

Research output: Contribution to journalReview articlepeer-review

157 Citations (Scopus)

Abstract

Several RNA virus genera belonging to the Virgaviridae and Flexiviridae families encode proteins organized in a triple gene block (TGB) that facilitate cell-to-cell and long-distance movement. The TGB proteins have been traditionally classified as hordei-like or potex-like based on phylogenetic comparisons and differences in movement mechanisms of the Hordeivirus and Potexvirus spp. However, accumulating data from other model viruses suggests that a revised framework is needed to accommodate the profound differences in protein interactions occurring during infection and ancillary capsid protein requirements for movement. The goal of this article is to highlight common features of the TGB proteins and salient differences in movement properties exhibited by individual viruses encoding these proteins. We discuss common and divergent aspects of the TGB transport machinery, describe putative nucleoprotein movement complexes, highlight recent data on TGB protein interactions and topological properties, and review membrane associations occurring during subcellular targeting and cell-to-cell movement. We conclude that the existing models cannot be used to explain all TGB viruses, and we propose provisional Potexvirus, Hordeivirus, and Pomovirus models. We also suggest areas that might profit from future research on viruses harboring this intriguing arrangement of movement proteins.

Original languageEnglish
Pages (from-to)1231-1247
Number of pages17
JournalMolecular Plant-Microbe Interactions
Volume23
Issue number10
DOIs
Publication statusPublished - Oct 2010

Keywords

  • CELL-TO-CELL
  • STRIPE-MOSAIC-VIRUS
  • YELLOW-VEIN-VIRUS
  • LONG-DISTANCE MOVEMENT
  • CYSTEINE-RICH PROTEIN
  • RNA-BINDING PROPERTIES
  • N-TERMINAL REGION
  • ACID IN-VITRO
  • COAT PROTEIN
  • SUBCELLULAR-LOCALIZATION

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