Abstract

YafO is a toxin encoded by the yafN-yafO antitoxin-toxin operon in the Escherichia coli genome. Our results show that YafO inhibits protein synthesis but not DNA or RNA synthesis. The in vivo [35S]methionine incorporation was inhibited within 5 min after YafO induction. In in vivo primer extension experiments with two different mRNAs, the specific cleavage bands appeared 11-13 bases downstream of the initiation codon, AUG, 2.5 min after the induction of YafO. An identical band was also detected in in vitro toeprinting experiments when YafO was added to the reaction mixture containing 70 S ribosomes and the same mRNAs even in the absence of tRNA(f)(Met). Notably, this band was not detected in the presence of YafO alone, indicating that YafO by itself does not have endoribonuclease activity under the conditions used. The full-length mRNAs almost completely disappeared 30 min after YafO induction in in vivo primer extension experiments, consistent with Northern blotting analysis. Over 84% of [35S]methionine-tRNA(f)(Met) was released from the translation initiation complex at 5.43 microM YafO in vitro. We demonstrated that the 70 S ribosome peak significantly increased upon YafO induction, and when the 70 S ribosomes dissociated into 50 and 30 S subunits, YafO was found to be associated with 50 S subunits. These results demonstrate that YafO is a ribosome-dependent mRNA interferase inhibiting protein synthesis.

Highlights

  • MazF and RelE are extensively studied toxin-antitoxin toxins in E. coli

  • These results indicate that YafO associates with 50 S subunits in 70 S ribosomes to effectively inhibit protein synthesis by cleaving mRNAs 11–13 bases downstream of the initiation codon

  • These results demonstrate that YafO inhibits protein synthesis, but not DNA replication or RNA synthesis

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Summary

Introduction

MazF and RelE are extensively studied toxin-antitoxin toxins in E. coli. Interestingly, RelE by itself has no endoribonuclease activity [4] and has been demonstrated to be a ribosome-associated factor that stimulates the endogenous ribonuclease activity of ribosomes [5]. These results indicate that YafO associates with 50 S subunits in 70 S ribosomes to effectively inhibit protein synthesis by cleaving mRNAs 11–13 bases downstream of the initiation codon.

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