Autoregulation of mazEF expression underlies growth heterogeneity in bacterial populations

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.

[1]  H. Engelberg-Kulka,et al.  An Escherichia coli chromosomal "addiction module" regulated by guanosine [corrected] 3',5'-bispyrophosphate: a model for programmed bacterial cell death. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[2]  N. W. Davis,et al.  The complete genome sequence of Escherichia coli K-12. , 1997, Science.

[3]  H. Bujard,et al.  Independent and tight regulation of transcriptional units in Escherichia coli via the LacR/O, the TetR/O and AraC/I1-I2 regulatory elements. , 1997, Nucleic acids research.

[4]  L. Serrano,et al.  Engineering stability in gene networks by autoregulation , 2000, Nature.

[5]  J. Keasling,et al.  Homogeneous expression of the P(BAD) promoter in Escherichia coli by constitutive expression of the low-affinity high-capacity AraE transporter. , 2001, Microbiology.

[6]  H. Engelberg-Kulka,et al.  Programmed Cell Death in Escherichia coli: Some Antibiotics Can Trigger mazEFLethality , 2001, Journal of bacteriology.

[7]  H. Engelberg-Kulka,et al.  The Regulation of the Escherichia coli mazEF Promoter Involves an Unusual Alternating Palindrome* , 2001, The Journal of Biological Chemistry.

[8]  U. Alon,et al.  Negative autoregulation speeds the response times of transcription networks. , 2002, Journal of molecular biology.

[9]  K. Gerdes,et al.  Rapid induction and reversal of a bacteriostatic condition by controlled expression of toxins and antitoxins , 2002, Molecular microbiology.

[10]  Mitsuhiko Ikura,et al.  MazF cleaves cellular mRNAs specifically at ACA to block protein synthesis in Escherichia coli. , 2003, Molecular cell.

[11]  S. Burley,et al.  Crystal structure of the MazE/MazF complex: molecular bases of antidote-toxin recognition. , 2003, Molecular cell.

[12]  K. Gerdes,et al.  Toxin-antitoxin loci as stress-response-elements: ChpAK/MazF and ChpBK cleave translated RNAs and are counteracted by tmRNA. , 2003, Journal of molecular biology.

[13]  H. Engelberg-Kulka,et al.  MazF-Mediated Cell Death in Escherichia coli: a Point of No Return , 2004, Journal of bacteriology.

[14]  H. Engelberg-Kulka,et al.  Escherichia coli mazEF-Mediated Cell Death Is Triggered by Various Stressful Conditions , 2004, Journal of bacteriology.

[15]  K. Gerdes,et al.  Prokaryotic toxin–antitoxin stress response loci , 2005, Nature Reviews Microbiology.

[16]  M. Inouye,et al.  Single protein production in living cells facilitated by an mRNA interferase. , 2005, Molecular cell.

[17]  N. Vázquez-Laslop,et al.  Increased Persistence in Escherichia coli Caused by Controlled Expression of Toxins or Other Unrelated Proteins , 2006, Journal of bacteriology.

[18]  Oscar P. Kuipers,et al.  Phenotypic variation in bacteria: the role of feedback regulation , 2006, Nature Reviews Microbiology.

[19]  L. Van Melderen,et al.  What Is the Benefit to Escherichia coli of Having Multiple Toxin-Antitoxin Systems in Its Genome? , 2007, Journal of bacteriology.

[20]  Nicolas E. Buchler,et al.  Molecular titration and ultrasensitivity in regulatory networks. , 2008, Journal of molecular biology.

[21]  Martin Overgaard,et al.  Messenger RNA interferase RelE controls relBE transcription by conditional cooperativity , 2008, Molecular microbiology.

[22]  E. Groisman,et al.  Positive feedback in cellular control systems , 2008, BioEssays : news and reviews in molecular, cellular and developmental biology.

[23]  T. Hwa,et al.  Growth Rate-Dependent Global Effects on Gene Expression in Bacteria , 2009, Cell.

[24]  H. Engelberg-Kulka,et al.  Escherichia coli MazF Leads to the Simultaneous Selective Synthesis of Both “Death Proteins” and “Survival Proteins” , 2009, PLoS genetics.

[25]  T. Tenson,et al.  The Escherichia coli mqsR and ygiT Genes Encode a New Toxin-Antitoxin Pair , 2010, Journal of bacteriology.

[26]  Andrew Wright,et al.  Robust Growth of Escherichia coli , 2010, Current Biology.

[27]  T. Hwa,et al.  Interdependence of Cell Growth and Gene Expression: Origins and Consequences , 2010, Science.

[28]  Paul J. Choi,et al.  Quantifying E. coli Proteome and Transcriptome with Single-Molecule Sensitivity in Single Cells , 2010, Science.

[29]  M. Elowitz,et al.  A synthetic three-color scaffold for monitoring genetic regulation and noise , 2010, Journal of biological engineering.

[30]  M. Inouye,et al.  Regulation of growth and death in Escherichia coli by toxin–antitoxin systems , 2011, Nature Reviews Microbiology.

[31]  N. Majdalani,et al.  The RpoS-mediated general stress response in Escherichia coli. , 2011, Annual review of microbiology.

[32]  K. Gerdes,et al.  Bacterial persistence by RNA endonucleases , 2011, Proceedings of the National Academy of Sciences.

[33]  T. Wood,et al.  Toxin-Antitoxin Systems Influence Biofilm and Persister Cell Formation and the General Stress Response , 2011, Applied and Environmental Microbiology.

[34]  L. Aravind,et al.  Interplay between gene expression noise and regulatory network architecture. , 2012, Trends in genetics : TIG.

[35]  U. Alon,et al.  A Genome-Wide Analysis of Promoter-Mediated Phenotypic Noise in Escherichia coli , 2012, PLoS genetics.

[36]  Eric Mjolsness,et al.  Measuring single-cell gene expression dynamics in bacteria using fluorescence time-lapse microscopy , 2011, Nature Protocols.

[37]  Kim Sneppen,et al.  Conditional cooperativity in toxin–antitoxin regulation prevents random toxin activation and promotes fast translational recovery , 2012, Nucleic acids research.

[38]  K. Gerdes,et al.  Bacterial persistence and toxin-antitoxin loci. , 2012, Annual review of microbiology.

[39]  T. Tenson,et al.  Transcriptional cross-activation between toxin-antitoxin systems of Escherichia coli , 2013, BMC Microbiology.

[40]  J. Geiselmann,et al.  Shared control of gene expression in bacteria by transcription factors and global physiology of the cell , 2013, Molecular systems biology.

[41]  Jan Danckaert,et al.  A General Model for Toxin-Antitoxin Module Dynamics Can Explain Persister Cell Formation in E. coli , 2013, PLoS Comput. Biol..

[42]  R. Varadarajan,et al.  MazF-induced Growth Inhibition and Persister Generation in Escherichia coli * , 2013, The Journal of Biological Chemistry.

[43]  Kim Sneppen,et al.  Conditional Cooperativity of Toxin - Antitoxin Regulation Can Mediate Bistability between Growth and Dormancy , 2013, PLoS Comput. Biol..

[44]  M. Inouye,et al.  Type II toxin-antitoxin loci: The mazEF family , 2013 .

[45]  Terence Hwa,et al.  Bacterial growth: global effects on gene expression, growth feedback and proteome partition. , 2014, Current opinion in biotechnology.

[46]  N. Woychik,et al.  An RNA-seq method for defining endoribonuclease cleavage specificity identifies dual rRNA substrates for toxin MazF-mt3 , 2014, Nature Communications.

[47]  L. Buts,et al.  Escherichia coli antitoxin MazE as transcription factor: insights into MazE-DNA binding , 2015, Nucleic acids research.

[48]  Kenneth C. Keiler,et al.  Mechanisms of ribosome rescue in bacteria , 2015, Nature Reviews Microbiology.

[49]  J. Rabinowitz,et al.  RNA Futile Cycling in Model Persisters Derived from MazF Accumulation , 2015, mBio.

[50]  L. Van Melderen,et al.  Regulatory crosstalk between type I and type II toxin-antitoxin systems in the human pathogen Enterococcus faecalis , 2015, RNA biology.

[51]  M. Muthuramalingam,et al.  Toxin-Antitoxin Modules Are Pliable Switches Activated by Multiple Protease Pathways , 2016, Toxins.

[52]  Tanel Tenson,et al.  Growth resumption from stationary phase reveals memory in Escherichia coli cultures , 2016, Scientific Reports.

[53]  Michael T. Wolfinger,et al.  The MazF-regulon: a toolbox for the post-transcriptional stress response in Escherichia coli , 2016, Nucleic acids research.

[54]  I. Moll,et al.  A Stress-Induced Bias in the Reading of the Genetic Code in Escherichia coli , 2016, mBio.

[55]  Rebecca Page,et al.  Toxin-antitoxin systems in bacterial growth arrest and persistence. , 2016, Nature chemical biology.

[56]  David W. Schryer,et al.  Toxins MazF and MqsR cleave Escherichia coli rRNA precursors at multiple sites , 2017, RNA biology.

[57]  Christopher J Petzold,et al.  Programming mRNA decay to modulate synthetic circuit resource allocation , 2016, Nature Communications.

[58]  I. Moll,et al.  MazF activation promotes translational heterogeneity of the grcA mRNA in Escherichia coli populations , 2017, PeerJ.

[59]  K. Gerdes,et al.  Retraction Notice to: (p)ppGpp Controls Bacterial Persistence by Stochastic Induction of Toxin-Antitoxin Activity , 2018, Cell.