Escherichia coli MazF leads to the simultaneous selective synthesis of both "death proteins" and "survival proteins"
The Escherichia coli mazEF module is one of the most thoroughly studied toxin-antitoxin systems. mazF encodes a stable toxin, MazF, and mazE encodes a labile antitoxin, MazE, which prevents the lethal effect of MazF. MazF is an endoribonuclease that leads to the inhibition of protein synthesis by cl...
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description | The Escherichia coli mazEF module is one of the most thoroughly studied toxin-antitoxin systems. mazF encodes a stable toxin, MazF, and mazE encodes a labile antitoxin, MazE, which prevents the lethal effect of MazF. MazF is an endoribonuclease that leads to the inhibition of protein synthesis by cleaving mRNAs at ACA sequences. Here, using 2D-gels, we show that in E. coli, although MazF induction leads to the inhibition of the synthesis of most proteins, the synthesis of an exclusive group of proteins, mostly smaller than about 20 kDa, is still permitted. We identified some of those small proteins by mass spectrometry. By deleting the genes encoding those proteins from the E. coli chromosome, we showed that they were required for the death of most of the cellular population. Under the same experimental conditions, which induce mazEF-mediated cell death, other such proteins were found to be required for the survival of a small sub-population of cells. Thus, MazF appears to be a regulator that induces downstream pathways leading to death of most of the population and the continued survival of a small sub-population, which will likely become the nucleus of a new population when growth conditions become less stressful. |
doi_str_mv | 10.1371/journal.pgen.1000390 |
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This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited: Amitai S, Kolodkin-Gal I, Hananya-Meltabashi M, Sacher A, Engelberg-Kulka H (2009) Escherichia coli MazF Leads to the Simultaneous Selective Synthesis of Both "Death Proteins" and "Survival Proteins". 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Kolodkin-Gal, Ilana ; Hananya-Meltabashi, Mirit ; Sacher, Ayelet ; Engelberg-Kulka, Hanna</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c765t-f1dc472678217d9c6765b8f8e24710959de5cac343737a5763ab64276267de423</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Apoptosis</topic><topic>DNA-Binding Proteins - physiology</topic><topic>E coli</topic><topic>Electrophoresis, Gel, Two-Dimensional</topic><topic>Endoribonucleases - physiology</topic><topic>Escherichia coli</topic><topic>Escherichia coli - cytology</topic><topic>Escherichia coli - growth & development</topic><topic>Escherichia coli Proteins - analysis</topic><topic>Escherichia coli Proteins - physiology</topic><topic>Genes</topic><topic>Genetic aspects</topic><topic>Genetics and Genomics</topic><topic>Genetics and Genomics/Gene Discovery</topic><topic>Genetics and Genomics/Gene Function</topic><topic>Health aspects</topic><topic>Mass Spectrometry</topic><topic>Messenger RNA</topic><topic>Microbial toxins</topic><topic>Microbiology</topic><topic>Microbiology/Microbial Physiology and Metabolism</topic><topic>Molecular Biology</topic><topic>Molecular Biology/Translational Regulation</topic><topic>Molecular weight</topic><topic>Physiological aspects</topic><topic>Population</topic><topic>Protein Biosynthesis</topic><topic>Protein synthesis</topic><topic>Proteins</topic><topic>Proteomics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Amitai, Shahar</creatorcontrib><creatorcontrib>Kolodkin-Gal, Ilana</creatorcontrib><creatorcontrib>Hananya-Meltabashi, Mirit</creatorcontrib><creatorcontrib>Sacher, Ayelet</creatorcontrib><creatorcontrib>Engelberg-Kulka, Hanna</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale In Context: Opposing Viewpoints</collection><collection>Gale In Context: Canada</collection><collection>Gale In Context: Science</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>PLoS genetics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Amitai, Shahar</au><au>Kolodkin-Gal, Ilana</au><au>Hananya-Meltabashi, Mirit</au><au>Sacher, Ayelet</au><au>Engelberg-Kulka, Hanna</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Escherichia coli MazF leads to the simultaneous selective synthesis of both "death proteins" and "survival proteins"</atitle><jtitle>PLoS genetics</jtitle><addtitle>PLoS Genet</addtitle><date>2009-03-01</date><risdate>2009</risdate><volume>5</volume><issue>3</issue><spage>e1000390</spage><epage>e1000390</epage><pages>e1000390-e1000390</pages><issn>1553-7404</issn><issn>1553-7390</issn><eissn>1553-7404</eissn><abstract>The Escherichia coli mazEF module is one of the most thoroughly studied toxin-antitoxin systems. mazF encodes a stable toxin, MazF, and mazE encodes a labile antitoxin, MazE, which prevents the lethal effect of MazF. MazF is an endoribonuclease that leads to the inhibition of protein synthesis by cleaving mRNAs at ACA sequences. Here, using 2D-gels, we show that in E. coli, although MazF induction leads to the inhibition of the synthesis of most proteins, the synthesis of an exclusive group of proteins, mostly smaller than about 20 kDa, is still permitted. We identified some of those small proteins by mass spectrometry. By deleting the genes encoding those proteins from the E. coli chromosome, we showed that they were required for the death of most of the cellular population. Under the same experimental conditions, which induce mazEF-mediated cell death, other such proteins were found to be required for the survival of a small sub-population of cells. Thus, MazF appears to be a regulator that induces downstream pathways leading to death of most of the population and the continued survival of a small sub-population, which will likely become the nucleus of a new population when growth conditions become less stressful.</abstract><cop>United States</cop><pub>Public Library of Science</pub><pmid>19282968</pmid><doi>10.1371/journal.pgen.1000390</doi><oa>free_for_read</oa></addata></record> |
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subjects | Apoptosis DNA-Binding Proteins - physiology E coli Electrophoresis, Gel, Two-Dimensional Endoribonucleases - physiology Escherichia coli Escherichia coli - cytology Escherichia coli - growth & development Escherichia coli Proteins - analysis Escherichia coli Proteins - physiology Genes Genetic aspects Genetics and Genomics Genetics and Genomics/Gene Discovery Genetics and Genomics/Gene Function Health aspects Mass Spectrometry Messenger RNA Microbial toxins Microbiology Microbiology/Microbial Physiology and Metabolism Molecular Biology Molecular Biology/Translational Regulation Molecular weight Physiological aspects Population Protein Biosynthesis Protein synthesis Proteins Proteomics |
title | Escherichia coli MazF leads to the simultaneous selective synthesis of both "death proteins" and "survival proteins" |
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