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Toxins  2014 

Toxin-Antitoxin Systems as Multilevel Interaction Systems

DOI: 10.3390/toxins6010304

Keywords: endoribonuclease, repression, trans-activation, proteolysis

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Abstract:

Toxin-antitoxin (TA) systems are small genetic modules usually composed of a toxin and an antitoxin counteracting the activity of the toxic protein. These systems are widely spread in bacterial and archaeal genomes. TA systems have been assigned many functions, ranging from persistence to DNA stabilization or protection against mobile genetic elements. They are classified in five types, depending on the nature and mode of action of the antitoxin. In type I and III, antitoxins are RNAs that either inhibit the synthesis of the toxin or sequester it. In type II, IV and V, antitoxins are proteins that either sequester, counterbalance toxin activity or inhibit toxin synthesis. In addition to these interactions between the antitoxin and toxin components (RNA-RNA, protein-protein, RNA-protein), TA systems interact with a variety of cellular factors, e.g., toxins target essential cellular components, antitoxins are degraded by RNAses or ATP-dependent proteases. Hence, TA systems have the capacity to interact with each other at different levels. In this review, we will discuss the different interactions in which TA systems are involved and their implications in TA system functions and evolution.

References

[1]  Ogura, T.; Hiraga, S. Mini-F plasmid genes that couple host cell division to plasmid proliferation. Proc. Natl. Acad. Sci. USA 1983, 80, 4784–4788, doi:10.1073/pnas.80.15.4784.
[2]  Gotfredsen, M.; Gerdes, K. The Escherichia coli relBE genes belong to a new toxin-antitoxin gene family. Mol. Microbiol. 1998, 29, 1065–1076, doi:10.1046/j.1365-2958.1998.00993.x.
[3]  Tsuchimoto, S.; Ohtsubo, H.; Ohtsubo, E. Two genes, pemK and pemI, responsible for stable maintenance of resistance plasmid R100. J. Bacteriol. 1988, 170, 1461–1466.
[4]  Jaffe, A.; Ogura, T.; Hiraga, S. Effects of the ccd function of the F plasmid on bacterial growth. J. Bacteriol. 1985, 163, 841–849.
[5]  Bravo, A.; de Torrontegui, G.; Diaz, R. Identification of components of a new stability system of plasmid R1, ParD, that is close to the origin of replication of this plasmid. Mol. Gen. Genet. 1987, 210, 101–110, doi:10.1007/BF00337764.
[6]  Masuda, Y.; Miyakawa, K.; Nishimura, Y.; Ohtsubo, E. chpA and chpB, Escherichia coli chromosomal homologs of the pem locus responsible for stable maintenance of plasmid R100. J. Bacteriol. 1993, 175, 6850–6856.
[7]  Leplae, R.; Geeraerts, D.; Hallez, R.; Guglielmini, J.; Drèze, P.; van Melderen, L. Diversity of bacterial type II toxin-antitoxin systems: A comprehensive search and functional analysis of novel families. Nucleic Acids Res. 2011, 39, 5513–5525, doi:10.1093/nar/gkr131.
[8]  Ramage, H.R.; Connolly, L.E.; Cox, J.S. Comprehensive functional analysis of Mycobacterium tuberculosis toxin-antitoxin systems: Implications for pathogenesis, stress responses, and evolution. PLoS Genet. 2009, 5, doi:10.1371/journal.pgen.1000767.
[9]  Peris-Bondia, F.; Van Melderen, L.; Université Libre de Bruxelles, Brussels, Belgium.. Unpublished data2013.
[10]  Hayes, F.; van Melderen, L. Toxins-antitoxins: Diversity, evolution and function. Crit. Rev. Biochem. Mol. Biol. 2011, 46, 386–408, doi:10.3109/10409238.2011.600437.
[11]  Brzozowska, I.; Zielenkiewicz, U. Regulation of toxin-antitoxin systems by proteolysis. Plasmid 2013, 70, 33–41, doi:10.1016/j.plasmid.2013.01.007.
[12]  Blower, T.R.; Salmond, G.P.; Luisi, B.F. Balancing at survival’s edge: The structure and adaptive benefits of prokaryotic toxin-antitoxin partners. Curr. Opin. Struct. Biol. 2011, 21, 109–118, doi:10.1016/j.sbi.2010.10.009.
[13]  Yamaguchi, Y.; Park, J.H.; Inouye, M. Toxin-antitoxin systems in Bacteria and Archaea. Annu. Rev. Genet. 2011, 45, 61–79, doi:10.1146/annurev-genet-110410-132412.
[14]  Van Melderen, L.; de Bast, M.S. Bacterial toxin-antitoxin systems: More than selfish entities? PLoS Genet. 2009, 5, doi:10.1371/journal.pgen.1000437.
[15]  Fineran, P.C.; Blower, T.R.; Foulds, I.J.; Humphreys, D.P.; Lilley, K.S.; Salmond, G.P. The phage abortive infection system, ToxIN, functions as a protein-RNA toxin-antitoxin pair. Proc. Natl. Acad. Sci. USA 2009, 106, 894–899.
[16]  Unterholzner, S.J.; Poppenberger, B.; Rozhon, W. Toxin-antitoxin systems: Biology, identification, and application. Mob Genet Elem. 2013, 3, doi:10.4161/mge.26219.
[17]  Fineran, P.C.; Blower, T.R.; Foulds, I.J.; Humphreys, D.P.; Lilley, K.S.; Salmond, G.P. The phage abortive infection system, ToxIN, functions as a protein-RNA toxin-antitoxin pair. Proc. Natl. Acad. Sci. USA 2009, 106, 894–899, doi:10.1073/pnas.0808832106.
[18]  Wang, X.; Lord, D.M.; Cheng, H.Y.; Osbourne, D.O.; Hong, S.H.; Sanchez-Torres, V.; Quiroga, C.; Zheng, K.; Herrmann, T.; Peti, W.; et al. A new type V toxin-antitoxin system where mRNA for toxin GhoT is cleaved by antitoxin GhoS. Nat. Chem. Biol. 2012, 8, 855–861, doi:10.1038/nchembio.1062.
[19]  Masuda, H.; Tan, Q.; Awano, N.; Wu, K.P.; Inouye, M. YeeU enhances the bundling of cytoskeletal polymers of MreB and FtsZ, antagonizing the CbtA (YeeV) toxicity in Escherichia coli. Mol. Microbiol. 2012, 84, 979–989, doi:10.1111/j.1365-2958.2012.08068.x.
[20]  Fozo, E.M.; Makarova, K.S.; Shabalina, S.A.; Yutin, N.; Koonin, E.V.; Storz, G. Abundance of type I toxin-antitoxin systems in bacteria: Searches for new candidates and discovery of novel families. Nucleic Acids Res. 2010, 38, 3743–3759, doi:10.1093/nar/gkq054.
[21]  Blower, T.R.; Pei, X.Y.; Short, F.L.; Fineran, P.C.; Humphreys, D.P.; Luisi, B.F.; Salmond, G.P. A processed noncoding RNA regulates an altruistic bacterial antiviral system. Nat. Struct. Mol. Biol. 2011, 18, 185–190, doi:10.1038/nsmb.1981.
[22]  Santos-Sierra, S.; Pardo-Abarrio, C.; Giraldo, R.; Díaz-Orejas, R. Genetic identification of two functional regions in the antitoxin of the parD killer system of plasmid R1. FEMS Microbiol. Lett. 2002, 206, 115–119, doi:10.1111/j.1574-6968.2002.tb10995.x.
[23]  Smith, J.A.; Magnuson, R.D. Modular organization of the Phd repressor/antitoxin protein. J. Bacteriol. 2004, 186, 2692–2698, doi:10.1128/JB.186.9.2692-2698.2004.
[24]  Bernard, P.; Couturier, M. The 41 carboxy-terminal residues of the miniF plasmid CcdA protein are sufficient to antagonize the killer activity of the CcdB protein. Mol. Gen. Genet. 1991, 226, 297–304, doi:10.1007/BF00273616.
[25]  Brown, B.L.; Grigoriu, S.; Kim, Y.; Arruda, J.M.; Davenport, A.; Wood, T.K.; Peti, W.; Page, R. Three dimensional structure of the MqsR:MqsA complex: A novel TA pair comprised of a toxin homologous to RelE and an antitoxin with unique properties. PLoS Pathog. 2009, 5, e1000706, doi:10.1371/journal.ppat.1000706.
[26]  Overgaard, M.; Borch, J.; J?rgensen, M.G.; Gerdes, K. Messenger RNA interferase RelE controls relBE transcription by conditional cooperativity. Mol. Microbiol. 2008, 69, 841–857, doi:10.1111/j.1365-2958.2008.06313.x.
[27]  Afif, H.; Allali, N.; Couturier, M.; van Melderen, L. The ratio between CcdA and CcdB modulates the transcriptional repression of the ccd poison-antidote system. Mol. Microbiol. 2001, 41, 73–82, doi:10.1046/j.1365-2958.2001.02492.x.
[28]  Tan, Q.; Awano, N.; Inouye, M. YeeV is an Escherichia coli toxin that inhibits cell division by targeting the cytoskeleton proteins, FtsZ and MreB. Mol. Microbiol. 2011, 79, 109–118, doi:10.1111/j.1365-2958.2010.07433.x.
[29]  Blower, T.R.; Short, F.L.; Rao, F.; Mizuguchi, K.; Pei, X.Y.; Fineran, P.C.; Luisi, B.F.; Salmond, G.P. Identification and classification of bacterial Type III toxin-antitoxin systems encoded in chromosomal and plasmid genomes. Nucleic Acids Res. 2012, 40, 6158–6173, doi:10.1093/nar/gks231.
[30]  Anantharaman, V.; Aravind, L. New connections in the prokaryotic toxin-antitoxin network: Relationship with the eukaryotic nonsense-mediated RNA decay system. Genome Biol. 2003, 4, R81, doi:10.1186/gb-2003-4-12-r81.
[31]  Goeders, N.; Dreze, P.L.; van Melderen, L. Relaxed cleavage specificity within the RelE toxin family. J. Bacteriol. 2013, 195, 2541–2549, doi:10.1128/JB.02266-12.
[32]  Schmidt, O.; Schuenemann, V.J.; Hand, N.J.; Silhavy, T.J.; Martin, J.; Lupas, A.N.; Djuranovic, S. prlF and yhaV encode a new toxin-antitoxin system in Escherichia coli. J. Mol. Biol. 2007, 372, 894–905, doi:10.1016/j.jmb.2007.07.016.
[33]  Fico, S.; Mahillon, J. TasA-tasB, a new putative toxin-antitoxin (TA) system from Bacillus thuringiensis pGI1 plasmid is a widely distributed composite mazE-doc TA system. BMC Genomics 2006, 7, 259, doi:10.1186/1471-2164-7-259.
[34]  Hallez, R.; Geeraerts, D.; Sterckx, Y.; Mine, N.; Loris, R.; van Melderen, L. New toxins homologous to ParE belonging to three-component toxin-antitoxin systems in Escherichia coli O157:H7. Mol. Microbiol. 2010, 76, 719–732, doi:10.1111/j.1365-2958.2010.07129.x.
[35]  Unoson, C.; Wagner, E.G. A small SOS-induced toxin is targeted against the inner membrane in Escherichia coli. Mol. Microbiol. 2008, 70, 258–270, doi:10.1111/j.1365-2958.2008.06416.x.
[36]  Weel-Sneve, R.; Kristiansen, K.I.; Odsbu, I.; Dalhus, B.; Booth, J.; Rognes, T.; Skarstad, K.; Bj?r?s, M. Single transmembrane peptide DinQ modulates membrane-dependent activities. PLoS Genet. 2013, 9, doi:10.1371/journal.pgen.1003260.
[37]  Silvaggi, J.M.; Perkins, J.B.; Losick, R. Small untranslated RNA antitoxin in Bacillus subtilis. J. Bacteriol. 2005, 187, 6641–6650, doi:10.1128/JB.187.19.6641-6650.2005.
[38]  Kawano, M.; Aravind, L.; Storz, G. An. antisense RNA controls synthesis of an SOS-induced toxin evolved from an antitoxin. Mol. Microbiol. 2007, 64, 738–754, doi:10.1111/j.1365-2958.2007.05688.x.
[39]  Arbing, M.A.; Handelman, S.K.; Kuzin, A.P.; Verdon, G.; Wang, C.; Su, M.; Rothenbacher, F.P.; Abashidze, M.; Liu, M.; Hurley, J.M.; et al. Crystal structures of Phd-Doc, HigA, and YeeU establish multiple evolutionary links between microbial growth-regulating toxin-antitoxin systems. Structure 2010, 18, 996–1010, doi:10.1016/j.str.2010.04.018.
[40]  Makarova, K.S.; Wolf, Y.I.; Koonin, E.V. Comprehensive comparative-genomic analysis of type 2 toxin-antitoxin systems and related mobile stress response systems in prokaryotes. Biol. Direct 2009, 4, 19, doi:10.1186/1745-6150-4-19.
[41]  Nolle, N.; Schuster, C.F.; Bertram, R. Two paralogous yefM-yoeB loci from Staphylococcus equorum encode functional toxin-antitoxin systems. Microbiology 2013, 159, 1575–1585, doi:10.1099/mic.0.068049-0.
[42]  Fiebig, A.; Castro Rojas, C.M.; Siegal-Gaskins, D.; Crosson, S. Interaction specificity, toxicity and regulation of a paralogous set of ParE/RelE-family toxin-antitoxin systems. Mol. Microbiol. 2010, 77, 236–251, doi:10.1111/j.1365-2958.2010.07207.x.
[43]  Ahidjo, B.A.; McKenzie, J.L.; Machowski, E.E.; Gordhan, B.G.; Arcus, V.; Abrahams, G.L.; Mizrahi, V. VapC toxins from Mycobacterium tuberculosis are ribonucleases that differentially inhibit growth and are neutralized by cognate VapB antitoxins. PLoS One 2011, 6, doi:10.1371/journal.pone.0021738.
[44]  Gupta, A. Killing activity and rescue function of genome-wide toxin-antitoxin loci of Mycobacterium tuberculosis. FEMS Microbiol. Lett. 2009, 290, 45–53, doi:10.1111/j.1574-6968.2008.01400.x.
[45]  Park, J.H.; Yoshizumi, S.; Yamaguchi, Y.; Wu, K.P.; Inouye, M. ACA-specific RNA sequence recognition is acquired via the loop 2 region of MazF mRNA interferase. Proteins 2013, 81, 874–883, doi:10.1002/prot.24246.
[46]  Tripathi, A.; Dewan, P.C.; Barua, B.; Varadarajan, R. Additional role for the ccd operon of F-plasmid as a transmissible persistence factor. Proc. Natl. Acad. Sci. USA 2012, 109, 12497–12502, doi:10.1073/pnas.1121217109.
[47]  Maisonneuve, E.; Shakespeare, L.J.; J?rgensen, M.G.; Gerdes, K. Bacterial persistence by RNA endonucleases. Proc. Natl. Acad. Sci. USA 2011, 108, 13206–13211.
[48]  Goeders, N.; Van Melderen, L. Université Libre de Bruxelles, Brussels, Belgium. Unpublished data, 2013.
[49]  Yang, M.; Gao, C.; Wang, Y.; Zhang, H.; He, Z.G. Characterization of the interaction and cross-regulation of three Mycobacterium tuberculosis RelBE modules. PLoS One 2010, 5, e10672.
[50]  Zhu, L.; Sharp, J.D.; Kobayashi, H.; Woychik, N.A.; Inouye, M. Noncognate Mycobacterium tuberculosis toxin-antitoxins can physically and functionally interact. J. Biol. Chem. 2010, 285, 39732–39738.
[51]  Korch, S.B.; Contreras, H.; Clark-Curtiss, J.E. Three Mycobacterium tuberculosis Rel toxin-antitoxin modules inhibit mycobacterial growth and are expressed in infected human macrophages. J. Bacteriol. 2009, 191, 1618–1630, doi:10.1128/JB.01318-08.
[52]  Singh, R.; Barry, C.E., 3rd; Boshoff, H.I. The three RelE homologs of Mycobacterium tuberculosis have individual, drug-specific effects on bacterial antibiotic tolerance. J. Bacteriol. 2010, 192, 1279–1291, doi:10.1128/JB.01285-09.
[53]  Kasari, V.; Mets, T.; Tenson, T.; Kaldalu, N. Transcriptional cross-activation between toxin-antitoxin systems of Escherichia coli. BMC Microbiol. 2013, 13, 45, doi:10.1186/1471-2180-13-45.
[54]  Bukowski, M.; Lyzen, R.; Helbin, W.M.; Bonar, E.; Szalewska-Palasz, A.; Wegrzyn, G.; Dubin, G.; Dubin, A.; Wladyka, B. A regulatory role for Staphylococcus aureus toxin-antitoxin system PemIKSa. Nat. Commun. 2013, 4, 2012, doi:10.1038/ncomms3012.
[55]  Wang, X.; Lord, D.M.; Hong, S.H.; Peti, W.; Benedik, M.J.; Page, R.; Wood, T.K. Type II toxin/antitoxin MqsR/MqsA controls type V toxin/antitoxin GhoT/GhoS. Environ. Microbiol. 2013, 15, 1734–1744, doi:10.1111/1462-2920.12063.
[56]  Garcia-Pino, A.; Christensen-Dalsgaard, M.; Wyns, L.; Yarmolinsky, M.; Magnuson, R.D.; Gerdes, K.; Loris, R. Doc of prophage P1 is inhibited by its antitoxin partner Phd through fold complementation. J. Biol. Chem. 2008, 283, 30821–30827, doi:10.1074/jbc.M805654200.
[57]  Winther, K.S.; Gerdes, K. Ectopic production of VapCs from Enterobacteria inhibits translation and trans-activates YoeB mRNA interferase. Mol. Microbiol. 2009, 72, 918–930, doi:10.1111/j.1365-2958.2009.06694.x.
[58]  Garcia-Pino, A.; Balasubramanian, S.; Wyns, L.; Gazit, E.; de Greve, H.; Magnuson, R.D.; Charlier, D.; van Nuland, N.A.; Loris, R. Allostery and intrinsic disorder mediate transcription regulation by conditional cooperativity. Cell 2010, 142, 101–111, doi:10.1016/j.cell.2010.05.039.
[59]  Guerout, A.M.; Iqbal, N.; Mine, N.; Ducos-Galand, M.; van Melderen, L.; Mazel, D. Characterization of the phd-doc and ccd toxin-antitoxin cassettes from Vibrio superintegrons. J. Bacteriol. 2013, 195, 2270–2283, doi:10.1128/JB.01389-12.
[60]  De Bast, M.S.; Mine, N.; van Melderen, L. Chromosomal toxin-antitoxin systems may act as antiaddiction modules. J. Bacteriol. 2008, 190, 4603–4609, doi:10.1128/JB.00357-08.
[61]  Polom, D.; Boss, L.; W?grzyn, G.; Hayes, F.; K?dzierska, B. Amino acid residues crucial for specificity of toxin-antitoxin interactions in the homologous Axe-Txe and YefM-YoeB complexes. FEBS J. 2013, 280, 5906–5918, doi:10.1111/febs.12517.
[62]  Wilbaux, M.; Mine, N.; Guérout, A.M.; Mazel, D.; van Melderen, L. Functional interactions between coexisting toxin-antitoxin systems of the ccd family in Escherichia coli O157:H7. J. Bacteriol. 2007, 189, 2712–2719, doi:10.1128/JB.01679-06.
[63]  Santos Sierra, S.; Giraldo, R.; Diaz Orejas, R. Functional interactions between chpB and parD, two homologous conditional killer systems found in the Escherichia coli chromosome and in plasmid R1. FEMS Microbiol. Lett. 1998, 168, 51–58, doi:10.1111/j.1574-6968.1998.tb13254.x.
[64]  Santos-Sierra, S.; Giraldo, R.; Diaz-Orejas, R. Functional interactions between homologous conditional killer systems of plasmid and chromosomal origin. FEMS Microbiol. Lett. 1997, 152, 51–56, doi:10.1111/j.1574-6968.1997.tb10408.x.
[65]  Mine, N.; Guglielmini, J.; Wilbaux, M.; van Melderen, L. The decay of the chromosomally encoded ccdO157 toxin-antitoxin system in the Escherichia coli species. Genetics 2009, 181, 1557–1566, doi:10.1534/genetics.108.095190.
[66]  Makarova, K.S.; Wolf, Y.I.; Koonin, E.V. Comparative genomics of defense systems in archaea and bacteria. Nucleic Acids Res. 2013, 41, 4360–1377, doi:10.1093/nar/gkt157.
[67]  Mruk, I.; Kobayashi, I. To be or not to be: Regulation of restriction-modification systems and other toxin-antitoxin systems. Nucleic. Acids Res. 2013, 13, 70–86.
[68]  Pecota, D.C.; Wood, T.K. Exclusion of T4 phage by the hok/sok killer locus from plasmid R1. J. Bacteriol. 1996, 178, 2044–2050.
[69]  Koga, M.; Otsuka, Y.; Lemire, S.; Yonesaki, T. Escherichia coli rnlA and rnlB compose a novel toxin-antitoxin system. Genetics 2011, 187, 123–130, doi:10.1534/genetics.110.121798.
[70]  Otsuka, Y.; Koga, M.; Iwamoto, A.; Yonesaki, T. A role of RnlA in the RNase LS activity from Escherichia coli. Genes Genet. Syst. 2007, 82, 291–299, doi:10.1266/ggs.82.291.
[71]  Otsuka, Y.; Yonesaki, T. Dmd of bacteriophage T4 functions as an antitoxin against Escherichia coli LsoA and RnlA toxins. Mol. Microbiol. 2012, 83, 669–681, doi:10.1111/j.1365-2958.2012.07975.x.
[72]  Blower, T.R.; Evans, T.J.; Przybilski, R.; Fineran, P.C.; Salmond, G.P. Viral evasion of a bacterial suicide system by RNA-based molecular mimicry enables infectious altruism. PLoS Genet. 2012, 8, doi:10.1371/journal.pgen.1003023.
[73]  Sberro, H.; Leavitt, A.; Kiro, R.; Koh, E.; Peleg, Y.; Qimron, U.; Sorek, R. Discovery of functional toxin/antitoxin systems in bacteria by shotgun cloning. Mol. Cell 2013, 50, 136–148, doi:10.1016/j.molcel.2013.02.002.
[74]  Christensen-Dalsgaard, M.; Jorgensen, M.G.; Gerdes, K. Three new RelE-homologous mRNA interferases of Escherichia coli differentially induced by environmental stresses. Mol. Microbiol. 2010, 75, 333–348, doi:10.1111/j.1365-2958.2009.06969.x.
[75]  Zhu, L.; Inoue, K.; Yoshizumi, S.; Kobayashi, H.; Zhang, Y.; Ouyang, M.; Kato, F.; Sugai, M.; Inouye, M. Staphylococcus aureus MazF specifically cleaves a pentad sequence, UACAU, which is unusually abundant in the mRNA for pathogenic adhesive factor SraP. J. Bacteriol. 2009, 191, 3248–3255, doi:10.1128/JB.01815-08.
[76]  Fu, Z.; Donegan, N.P.; Memmi, G.; Cheung, A.L. Characterization of MazFSa, an endoribonuclease from Staphylococcus aureus. J. Bacteriol. 2007, 189, 8871–8879, doi:10.1128/JB.01272-07.
[77]  Zhu, L.; Phadtare, S.; Nariya, H.; Ouyang, M.; Husson, R.N.; Inouye, M. The mRNA interferases, MazF-mt3 and MazF-mt7 from Mycobacterium tuberculosis target unique pentad sequences in single-stranded RNA. Mol. Microbiol. 2008, 69, 559–569, doi:10.1111/j.1365-2958.2008.06284.x.
[78]  Schifano, J.M.; Edifor, R.; Sharp, J.D.; Ouyang, M.; Konkimalla, A.; Husson, R.N.; Woychik, N.A. Mycobacterial toxin MazF-mt6 inhibits translation through cleavage of 23S rRNA at the ribosomal A site. Proc. Natl. Acad. Sci. USA 2013, 110, 8501–8506.
[79]  Jurenaite, M.; Markuckas, A.; Suziedeliene, E. Identification and characterization of type II toxin-antitoxin systems in the opportunistic pathogen Acinetobacter baumannii. J. Bacteriol. 2013, 195, 3165–3172, doi:10.1128/JB.00237-13.
[80]  Hurley, J.M.; Cruz, J.W.; Ouyang, M.; Woychik, N.A. Bacterial toxin RelE mediates frequent codon-independent mRNA cleavage from the 5' end of coding regions in vivo. J. Biol. Chem. 2011, 286, 14770–14778.
[81]  Armalyte, J.; Jurenaite, M.; Beinoraviciūte, G.; Teiserskas, J.; Suziedeliene, E. Characterization of Escherichia coli dinJ-yafQ toxin-antitoxin system using insights from mutagenesis data. J. Bacteriol. 2012, 194, 1523–1532, doi:10.1128/JB.06104-11.
[82]  Prysak, M.H.; Mozdzierz, C.J.; Cook, A.M.; Zhu, L.; Zhang, Y.; Inouye, M.; Woychik, N.A. Bacterial toxin YafQ is an endoribonuclease that associates with the ribosome and blocks translation elongation through sequence-specific and frame-dependent mRNA cleavage. Mol. Microbiol. 2009, 71, 1071–1087, doi:10.1111/j.1365-2958.2008.06572.x.
[83]  Zhang, Y.; Inouye, M. The inhibitory mechanism of protein synthesis by YoeB, an Escherichia coli toxin. J. Biol. Chem. 2009, 284, 6627–6638, doi:10.1074/jbc.M808779200.
[84]  Hurley, J.M.; Woychik, N.A. Bacterial toxin HigB associates with ribosomes and mediates translation-dependent mRNA cleavage at A-rich sites. J. Biol. Chem. 2009, 284, 18605–18613, doi:10.1074/jbc.M109.008763.
[85]  Zhang, Y.; Inouye, M. RatA (YfjG), an Escherichia coli toxin, inhibits 70S ribosome association to block translation initiation. Mol. Microbiol. 2011, 79, 1418–1429, doi:10.1111/j.1365-2958.2010.07506.x.
[86]  Yamaguchi, Y.; Park, J.H.; Inouye, M. MqsR, a crucial regulator for quorum sensing and biofilm formation, is a GCU-specific mRNA interferase in Escherichia coli. J. Biol. Chem. 2009, 284, 28746–28753, doi:10.1074/jbc.M109.032904.
[87]  Heaton, B.E.; Herrou, J.; Blackwell, A.E.; Wysocki, V.H.; Crosson, S. Molecular structure and function of the novel BrnT/BrnA toxin-antitoxin system of Brucella abortus. J. Biol. Chem. 2012, 287, 12098–12110.
[88]  Han, K.D.; Matsuura, A.; Ahn, H.C.; Kwon, A.R.; Min, Y.H.; Park, H.J.; Won, H.S.; Park, S.J.; Kim, D.Y.; Lee, B.J. Functional identification of toxin-antitoxin molecules from Helicobacter pylori 26695 and structural elucidation of the molecular interactions. J. Biol. Chem. 2011, 286, 4842–4853, doi:10.1074/jbc.M109.097840.
[89]  Zhang, Y.; Zhang, J.; Hoeflich, K.P.; Ikura, M.; Qing, G.; Inouye, M. MazF cleaves cellular mRNAs specifically at ACA to block protein synthesis in Escherichia coli. Mol. Cell 2003, 12, 913–923, doi:10.1016/S1097-2765(03)00402-7.
[90]  Yamaguchi, Y.; Nariya, H.; Park, J.H.; Inouye, M. Inhibition of specific gene expressions by protein-mediated mRNA interference. Nat. Commun. 2012, 3, 607, doi:10.1038/ncomms1621.
[91]  Pimentel, B.; Madine, M.A.; de la Cueva-Mendez, G. Kid cleaves specific mRNAs at UUACU sites to rescue the copy number of plasmid R1. EMBO J. 2005, 24, 3459–3469, doi:10.1038/sj.emboj.7600815.
[92]  Wei, Y.; Gao, Z.Q.; Otsuka, Y.; Naka, K.; Yonesaki, T.; Zhang, H.; Dong, Y.H. Structure-function studies of Escherichia coli RnlA reveal a novel toxin structure involved in bacteriophage resistance. Mol. Microbiol. 2013, 90, 956–965, doi:10.1111/mmi.12409.
[93]  Winther, K.S.; Gerdes, K. Enteric virulence associated protein VapC inhibits translation by cleavage of initiator tRNA. Proc. Natl. Acad. Sci. USA 2011, 108, 7403–7407, doi:10.1073/pnas.1019587108.
[94]  Castro-Roa, D.; Garcia-Pino, A.; de Gieter, S.; van Nuland, N.A.; Loris, R.; Zenkin, N. The Fic protein Doc uses an inverted substrate to phosphorylate and inactivate EF-Tu. Nat. Chem. Biol. 2013, 9, 811–817, doi:10.1038/nchembio.1364.
[95]  Schumacher, M.A.; Piro, K.M.; Xu, W.; Hansen, S.; Lewis, K.; Brennan, R.G. Molecular mechanisms of HipA-mediated multidrug tolerance and its neutralization by HipB. Science 2009, 323, 396–401, doi:10.1126/science.1163806.
[96]  Germain, E.; Castro-Roa, D.; Zenkin, N.; Gerdes, K. Molecular mechanism of bacterial persistence by HipA. Mol. Cell 2013, 52, 248–254, doi:10.1016/j.molcel.2013.08.045.
[97]  Maki, S.; Takiguchi, S.; Miki, T.; Horiuchi, T. Modulation of DNA supercoiling activity of Escherichia coli DNA gyrase by F plasmid proteins. Antagonistic actions of LetA (CcdA) and LetD (CcdB) proteins. J. Biol. Chem. 1992, 267, 12244–12251.
[98]  Dao-Thi, M.H.; van Melderen, L.; de Genst, E.; Afif, H.; Buts, L.; Wyns, L.; Loris, R. Molecular basis of gyrase poisoning by the addiction toxin CcdB. J. Mol. Biol. 2005, 348, 1091–1102, doi:10.1016/j.jmb.2005.03.049.
[99]  Jiang, Y.; Pogliano, J.; Helinski, D.R.; Konieczny, I. ParE toxin encoded by the broad-host-range plasmid RK2 is an inhibitor of Escherichia coli gyrase. Mol. Microbiol. 2002, 44, 971–979, doi:10.1046/j.1365-2958.2002.02921.x.
[100]  Yuan, J.; Sterckx, Y.; Mitchenall, L.A.; Maxwell, A.; Loris, R.; Waldor, M.K. Vibrio cholerae ParE2 poisons DNA gyrase via a mechanism distinct from other gyrase inhibitors. J. Biol. Chem. 2010, 285, 40397–40408, doi:10.1074/jbc.M110.138776.
[101]  Bernard, P.; Couturier, M. Cell killing by the F plasmid CcdB protein involves poisoning of DNA-topoisomerase II complexes. J. Mol. Biol. 1992, 226, 735–745, doi:10.1016/0022-2836(92)90629-X.
[102]  Miki, T.; Orita, T.; Furuno, M.; Horiuchi, T. Control. of cell division by sex factor F in Escherichia coli. III. Participation of the groES (mopB) gene of the host bacteria. J. Mol. Biol. 1988, 201, 327–338, doi:10.1016/0022-2836(88)90141-6.
[103]  Mutschler, H.; Gebhardt, M.; Shoeman, R.L.; Meinhart, A. A novel mechanism of programmed cell death in bacteria by toxin-antitoxin systems corrupts peptidoglycan synthesis. PLoS Biol. 2011, 9, doi:10.1371/journal.pbio.1001033.
[104]  Fozo, E.M.; Hemm, M.R.; Storz, G. Small toxic proteins and the antisense RNAs that repress them. Microbiol. Mol. Biol. Rev. 2008, 72, 579–589, doi:10.1128/MMBR.00025-08.
[105]  Zielenkiewicz, U.; Ceglowski, P. The toxin-antitoxin system of the streptococcal plasmid pSM19035. J. Bacteriol. 2005, 187, 6094–6105, doi:10.1128/JB.187.17.6094-6105.2005.
[106]  Meinhart, A.; Alonso, J.C.; Str?ter, N.; Saenger, W. Crystal structure of the plasmid maintenance system epsilon/zeta: Functional mechanism of toxin zeta and inactivation by epsilon 2 zeta 2 complex formation. Proc. Natl. Acad. Sci. USA 2003, 100, 1661–1666, doi:10.1073/pnas.0434325100.
[107]  Cataudella, I.; Sneppen, K.; Gerdes, K.; Mitarai, N. Conditional cooperativity of toxin—Antitoxin regulation can mediate bistability between growth and dormancy. PLoS Comput. Biol. 2013, 9, doi:10.1371/journal.pcbi.1003174.
[108]  Gelens, L.; Hill, L.; Vandervelde, A.; Danckaert, J.; Loris, R. A general model for toxin-antitoxin module dynamics can explain persister cell formation in E. coli. PLoS Comput. Biol. 2013, 9, doi:10.1371/journal.pcbi.1003190.
[109]  Boss, L.; Labudda, ?.; W?grzyn, G.; Hayes, F.; K?dzierska, B. The axe-txe complex of Enterococcus faecium presents a multilayered mode of toxin-antitoxin gene expression regulation. PLoS One 2013, 8, doi:10.1371/journal.pone.0073569.
[110]  Brown, B.L.; Lord, D.M.; Grigoriu, S.; Peti, W.; Page, R. The Escherichia coli toxin MqsR destabilizes the transcriptional repression complex formed between the antitoxin MqsA and the mqsRA operon promoter. J. Biol. Chem. 2013, 288, 1286–1294, doi:10.1074/jbc.M112.421008.
[111]  Madl, T.; van Melderen, L.; Mine, N.; Respondek, M.; Oberer, M.; Keller, W.; Khatai, L.; Zangger, K. Structural basis for nucleic acid and toxin recognition of the bacterial antitoxin CcdA. J. Mol. Biol. 2006, 364, 170–185, doi:10.1016/j.jmb.2006.08.082.
[112]  Kamada, K.; Hanaoka, F.; Burley, S.K. Crystal structure of the MazE/MazF complex: Molecular bases of antidote-toxin recognition. Mol. Cell 2003, 11, 875–884, doi:10.1016/S1097-2765(03)00097-2.
[113]  Oberer, M.; Zangger, K.; Gruber, K.; Keller, W. The solution structure of ParD, the antidote of the ParDE toxin antitoxin module, provides the structural basis for DNA and toxin binding. Protein Sci. 2007, 16, 1676–1688, doi:10.1110/ps.062680707.
[114]  Li, G.Y.; Zhang, Y.; Inouye, M.; Ikura, M. Structural mechanism of transcriptional autorepression of the Escherichia coli RelB/RelE antitoxin/toxin module. J. Mol. Biol. 2008, 380, 107–119, doi:10.1016/j.jmb.2008.04.039.
[115]  Dienemann, C.; B?ggild, A.; Winther, K.S.; Gerdes, K.; Brodersen, D.E. Crystal structure of the VapBC toxin-antitoxin complex from Shigella flexneri reveals a hetero-octameric DNA-binding assembly. J. Mol. Biol. 2011, 414, 713–722, doi:10.1016/j.jmb.2011.10.024.
[116]  Marianovsky, I.; Aizenman, E.; Engelberg-Kulka, H.; Glaser, G. The regulation of the Escherichia coli mazEF promoter involves an unusual alternating palindrome. J. Biol. Chem. 2001, 276, 5975–5984.
[117]  Lin, C.-Y.; Awano, N.; Masuda, H.; Park, J.-H.; Inouye, M. Transcriptional repressor HipB regulates the multiple promoters in Escherichia coli. J. Mol. Microbiol. Biotechnol. 2013, 23, 440–447, doi:10.1159/000354311.
[118]  Wang, X.; Kim, Y.; Hong, S.H.; Ma, Q.; Brown, B.L.; Pu, M.; Tarone, A.M.; Benedik, M.J.; Peti, W.; Page, R.; et al. Antitoxin MqsA helps mediate the bacterial general stress response. Nat. Chem. Biol. 2011, 7, 359–366, doi:10.1038/nchembio.560.
[119]  Soo, V.W.; Wood, T.K. Antitoxin MqsA represses curli formation through the master biofilm regulator CsgD. Sci. Rep. 2013, 3, 3186.
[120]  Kim, Y.; Wang, X.; Zhang, X.S.; Grigoriu, S.; Page, R.; Peti, W.; Wood, T.K. Escherichia coli toxin/antitoxin pair MqsR/MqsA regulate toxin CspD. Environ. Microbiol. 2010, 12, 1105–1121.
[121]  Hu, Y.; Benedik, M.J.; Wood, T.K. Antitoxin DinJ influences the general stress response through transcript stabilizer CspE. Environ. Microbiol. 2012, 14, 669–679.
[122]  Korch, S.B.; Henderson, T.A.; Hill, T.M. Characterization of the hipA7 allele of Escherichia coli and evidence that high persistence is governed by (p)ppGpp synthesis. Mol. Microbiol. 2003, 50, 1199–1213, doi:10.1046/j.1365-2958.2003.03779.x.
[123]  Van Melderen, L.; Thi, M.H.; Lecchi, P.; Gottesman, S.; Couturier, M.; Maurizi, M.R. ATP-dependent degradation of CcdA by Lon protease. Effects of secondary structure and heterologous subunit interactions. J. Biol. Chem. 1996, 271, 27730–27738.
[124]  Maisonneuve, E.; Castro-Camargo, M.; Gerdes, K. (p)ppGpp controls bacterial persistence by stochastic induction of toxin-antitoxin activity. Cell 2013, 154, 1140–1150, doi:10.1016/j.cell.2013.07.048.
[125]  Bordes, P.; Cirinesi, A.M.; Ummels, R.; Sala, A.; Sakr, S.; Bitter, W.; Genevaux, P. SecB-like chaperone controls a toxin-antitoxin stress-responsive system in Mycobacterium tuberculosis. Proc. Natl. Acad. Sci. USA 2011, 108, 8438–8443, doi:10.1073/pnas.1101189108.
[126]  Jahn, N.; Preis, H.; Wiedemann, C.; Brantl, S. BsrG/SR4 from Bacillus subtilis—The first temperature-dependent type I toxin-antitoxin system. Mol. Microbiol. 2012, 83, 579–598, doi:10.1111/j.1365-2958.2011.07952.x.
[127]  Gerdes, K.; Nielsen, A.; Thorsted, P.; Wagner, E.G. Mechanism of killer gene activation. Antisense RNA-dependent RNase III cleavage ensures rapid turn-over of the stable hok, srnB and pndA effector messenger RNAs. J. Mol. Biol. 1992, 226, 637–649, doi:10.1016/0022-2836(92)90621-P.
[128]  Dam Mikkelsen, N.; Gerdes, K. Sok antisense RNA from plasmid R1 is functionally inactivated by RNase E and polyadenylated by poly(A) polymerase I. Mol. Microbiol. 1997, 26, 311–320, doi:10.1046/j.1365-2958.1997.5751936.x.
[129]  Durand, S.; Gilet, L.; Condon, C. The essential function of B. subtilis RNase III is to silence foreign toxin genes. PLoS Genet. 2012, 8, doi:10.1371/journal.pgen.1003181.

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