Photochemical cross-linking of influenza A polymerase to its virion RNA promoter defines a polymerase binding site at residues 9 to 12 of the promoter

J Gen Virol. 1993 Jul:74 ( Pt 7):1327-33. doi: 10.1099/0022-1317-74-7-1327.

Abstract

A previous study of the 12 nucleotide-long influenza A virion RNA promoter has shown that three nucleotides, residues 9 to 11, were crucial for transcription in vitro, although other nucleotides play a significant but less important role. A model for polymerase-promoter recognition was proposed, according to which there were two sites: a binding site at residues 9 to 11 and a regulatory site at or near the site of initiation at residue 1. By studying the effect of point mutations in the promoter on the binding efficiency of the polymerase using a photochemical cross-linking assay, we now show that residues 9 to 12 are crucial for binding. In addition residues 4 to 8, though not as important, are involved in binding, possibly by stabilizing the polymerase-promoter complex. Both PB1 and PB2 apparently play an important role during virion RNA promoter recognition and binding.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Base Sequence
  • Binding Sites
  • Binding, Competitive
  • Conserved Sequence
  • Cross-Linking Reagents
  • DNA-Directed RNA Polymerases / genetics
  • DNA-Directed RNA Polymerases / metabolism*
  • Influenza A virus / enzymology*
  • Influenza A virus / genetics*
  • Kinetics
  • Molecular Sequence Data
  • Mutagenesis, Insertional
  • Mutagenesis, Site-Directed
  • Photochemistry
  • Point Mutation
  • Promoter Regions, Genetic*
  • RNA, Viral / genetics
  • RNA, Viral / metabolism*
  • Rabbits / immunology
  • Templates, Genetic
  • Virion / enzymology
  • Virion / genetics*

Substances

  • Cross-Linking Reagents
  • RNA, Viral
  • DNA-Directed RNA Polymerases