Abstract

The MazF toxin sequence-specifically cleaves single-stranded RNA upon various stressful conditions, and it is activated as a part of the mazEF toxin–antitoxin module in Escherichia coli. Although autoregulation of mazEF expression through the MazE antitoxin-dependent transcriptional repression has been biochemically characterized, less is known about post-transcriptional autoregulation, as well as how both of these autoregulatory features affect growth of single cells during conditions that promote MazF production. Here, we demonstrate post-transcriptional autoregulation of mazF expression dynamics by MazF cleaving its own transcript. Single-cell analyses of bacterial populations during ectopic MazF production indicated that two-level autoregulation of mazEF expression influences cell-to-cell growth rate heterogeneity. The increase in growth rate heterogeneity is governed by the MazE antitoxin, and tuned by the MazF-dependent mazF mRNA cleavage. Also, both autoregulatory features grant rapid exit from the stress caused by mazF overexpression. Time-lapse microscopy revealed that MazF-mediated cleavage of mazF mRNA leads to increased temporal variability in length of individual cells during ectopic mazF overexpression, as explained by a stochastic model indicating that mazEF mRNA cleavage underlies temporal fluctuations in MazF levels during stress.

Highlights

  • MazF is the toxin component of the mazEF toxin-antitoxin (TA) system, which is a type II TA locus [1, 2, 3]

  • Growth modulation during prolonged mazF overexpression occurs in two phases: an initial transient growth cessation caused by large amount of free toxin, followed by antitoxin-dependent growth rescue

  • In this study we investigated how autoregulation of mazEF expression at the transcriptional and post-transcriptional level affects growth of E. coli populations and single cells during ectopic mazF expression, as well as during recovery after stress caused by mazF expression

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Summary

Introduction

MazF is the toxin component of the mazEF toxin-antitoxin (TA) system, which is a type II TA locus [1, 2, 3]. The mazF gene encodes an endoribonuclease that sequence- cleaves single-stranded RNA at ACA sites in E. coli [4], and mazE encodes the unstable antitoxin that is co-expressed with mazF. Under non-stressful conditions, MazF is inactivated by a sandwich-like complex consisting of two homodimers of MazF and one homodimer of. The activity of the proteases ClpAP [6, 7] and Lon [8] is increased, 17 resulting in fast degradation of MazE thereby allowing MazF to exert its function, which leads to reduction in overall translation and inhibition of bacterial growth [9]. MazF-mediated RNA cleavage occurs in the presence of antibiotics that are general inhibitors of transcription (rifampicin) or translation (chloramphenicol and spectinomycin) [12]

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