Qbeta-phage resistance by deletion of the coiled-coil motif in elongation factor Ts

J Biol Chem. 2004 Jan 16;279(3):1878-84. doi: 10.1074/jbc.M306605200. Epub 2003 Oct 28.

Abstract

Elongation factor Ts (EF-Ts) is the guanine-nucleotide exchange factor of elongation factor Tu (EF-Tu), which promotes the binding of aminoacyl-tRNA to the mRNA-programmed ribosome in prokaryotes. The EF-Tu.EF-Ts complex, one of the EF-Tu complexes during protein synthesis, is also a component of RNA-dependent RNA polymerases like the polymerase from coliphage Qbeta. The present study shows that the Escherichia coli mutant GRd.tsf lacking the coiled-coil motif of EF-Ts is completely resistant to phage Qbeta and that Qbeta-polymerase complex formation is not observed. GRd.tsf is the first E. coli mutant ever described that is unable to form a Qbeta-polymerase complex while still maintaining an almost normal growth behavior. The phage resistance correlates with an observed instability of the mutant EF-Tu.EF-Ts complex in the presence of guanine nucleotides. Thus, the mutant EF-Tu.EF-Ts is the first EF-Tu.EF-Ts complex ever described that is completely inactive in the Qbeta-polymerase complex despite its almost full activity in protein synthesis. We propose that the role of EF-Ts in the Qbeta-polymerase complex is to control and trap EF-Tu in a stable conformation with affinity for RNA templates while unable to bind aminoacyl-tRNA.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Coliphages / physiology*
  • DNA-Directed RNA Polymerases / metabolism
  • Escherichia coli / virology*
  • Escherichia coli Proteins / physiology*
  • Peptide Elongation Factors / chemistry
  • Peptide Elongation Factors / physiology*
  • Protein Biosynthesis
  • Protein Conformation
  • RNA, Viral / biosynthesis
  • Virus Replication

Substances

  • Escherichia coli Proteins
  • Peptide Elongation Factors
  • RNA, Viral
  • elongation factor Ts
  • DNA-Directed RNA Polymerases