The structure of native influenza virion ribonucleoproteins

Science. 2012 Dec 21;338(6114):1634-7. doi: 10.1126/science.1228172. Epub 2012 Nov 22.

Abstract

The influenza viruses cause annual epidemics of respiratory disease and occasional pandemics, which constitute a major public-health issue. The segmented negative-stranded RNAs are associated with the polymerase complex and nucleoprotein (NP), forming ribonucleoproteins (RNPs), which are responsible for virus transcription and replication. We describe the structure of native RNPs derived from virions. They show a double-helical conformation in which two NP strands of opposite polarity are associated with each other along the helix. Both strands are connected by a short loop at one end of the particle and interact with the polymerase complex at the other end. This structure will be relevant for unraveling the mechanisms of nuclear import of parental virus RNPs, their transcription and replication, and the encapsidation of progeny RNPs into virions.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Nucleus / metabolism
  • Cell Nucleus / virology
  • Cryoelectron Microscopy
  • Electron Microscope Tomography
  • Image Processing, Computer-Assisted
  • Influenza A Virus, H1N1 Subtype / chemistry*
  • Influenza A Virus, H1N1 Subtype / physiology
  • Influenza A Virus, H1N1 Subtype / ultrastructure
  • Madin Darby Canine Kidney Cells
  • Microscopy, Electron
  • Models, Molecular
  • Nucleocapsid Proteins
  • Protein Conformation
  • Protein Structure, Secondary
  • RNA, Viral / chemistry*
  • RNA, Viral / metabolism
  • RNA-Binding Proteins / chemistry
  • RNA-Binding Proteins / metabolism
  • RNA-Binding Proteins / ultrastructure
  • RNA-Dependent RNA Polymerase / chemistry
  • RNA-Dependent RNA Polymerase / metabolism
  • RNA-Dependent RNA Polymerase / ultrastructure
  • Ribonucleoproteins / chemistry*
  • Ribonucleoproteins / metabolism
  • Ribonucleoproteins / ultrastructure
  • Transcription, Genetic
  • Viral Core Proteins / chemistry
  • Viral Core Proteins / metabolism
  • Viral Core Proteins / ultrastructure
  • Viral Proteins / chemistry*
  • Viral Proteins / metabolism
  • Viral Proteins / ultrastructure
  • Virion / chemistry*
  • Virion / ultrastructure

Substances

  • NP protein, Influenza A virus
  • Nucleocapsid Proteins
  • RNA, Viral
  • RNA-Binding Proteins
  • Ribonucleoproteins
  • Viral Core Proteins
  • Viral Proteins
  • RNA-Dependent RNA Polymerase

Associated data

  • PDB/4BBL