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bacteria:t3e:avrbs3 [2020/08/27 11:00] stbacteria:t3e:avrbs3 [2025/02/21 12:08] (current) joana_costa
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-====== AvrBs3 ======+====== The Type III Effector AvrBs3 from //Xanthomonas// ======
  
 Author: [[https://www.researchgate.net/profile/Nay_Dia2|Nay C. Dia]]\\ Author: [[https://www.researchgate.net/profile/Nay_Dia2|Nay C. Dia]]\\
 Internal reviewer: [[https://www.genetik.uni-hannover.de/boch.html|Jens Boch]]\\ Internal reviewer: [[https://www.genetik.uni-hannover.de/boch.html|Jens Boch]]\\
-Expert reviewer: FIXME+Expert reviewer: [[https://www.researchgate.net/profile/Sabine_Thieme3|Sabine Thieme]]
  
 Class: AvrBs3\\ Class: AvrBs3\\
 Family: Transcription Activator-Like (TAL) Effectors, TALEs (previously: AvrBs3/PthA)\\ Family: Transcription Activator-Like (TAL) Effectors, TALEs (previously: AvrBs3/PthA)\\
 Prototype: AvrBs3 (//Xanthomonas euvesicatoria// pv. //euvesicatoria//, ex //Xanthomonas campestris// pv. //vesicatoria//; strain 71-21)\\ Prototype: AvrBs3 (//Xanthomonas euvesicatoria// pv. //euvesicatoria//, ex //Xanthomonas campestris// pv. //vesicatoria//; strain 71-21)\\
-RefSeq ID: [[https://www.ncbi.nlm.nih.gov/protein/P14727.2|P14727.2]] (1164 aa)\\ +GenBank ID: [[https://www.ncbi.nlm.nih.gov/protein/P14727.2|P14727.2]] (1164 aa)\\ 
-3D structure: [[https://www.rcsb.org/structure/2KQ5|2KQ5]] (Murakami //et al.//, 2010); [[https://www.rcsb.org/structure/3V6P|3V6P]], [[https://www.rcsb.org/structure/3V6T| 3V6T ]] (Deng //et al.//, 2012a); [[https://www.rcsb.org/structure/4GJP|4GJP]], [[https://www.rcsb.org/structure/4GJR|4GJR]] (Deng //et al.//, 2012b); [[https://www.rcsb.org/structure/4HPZ|4HPZ]] (Gao //et al.//, 2012) ; [[https://www.rcsb.org/structure/3UGM|3UGM]] (Mak //et al.//, 2012); [[https://www.rcsb.org/structure/4GG4|4GG4]] (Yin //et al.//, 2012); [[https://www.rcsb.org/structure/2YPF|2YPF ]] (Stella //et al//., 2013); [[https://www.rcsb.org/structure/4OSH|4OSH]], [[https://www.rcsb.org/structure/4OSI| 4OSI]], [[https://www.rcsb.org/structure/4OSJ| 4OSJ]], [[https://www.rcsb.org/structure/4OSK| 4OSK]], [[https://www.rcsb.org/structure/4OSL| 4OSL]], [[https://www.rcsb.org/structure/4OSM| 4OSM]], [[https://www.rcsb.org/structure/4OSQ|4OSQ]], [[https://www.rcsb.org/structure/4OSR|4OSR]], [[https://www.rcsb.org/structure/4OSS|4OSS]], [[https://www.rcsb.org/structure/4OST| 4OST]], [[https://www.rcsb.org/structure/4OSV| 4OSV]], [[https://www.rcsb.org/structure/4OSW| 4OSW]], [[https://www.rcsb.org/structure/4OSZ| 4OSZ]], [[https://www.rcsb.org/structure/4OT0| 4OT0]], [[https://www.rcsb.org/structure/4OT3| 4OT3]], [[https://www.rcsb.org/structure/4OTO|4OTO]] (Deng //et al.//, 2014); [[https://www.rcsb.org/structure/6JTQ|6JTQ]], [[https://www.rcsb.org/structure/6JVZ|6JVZ]], [[https://www.rcsb.org/structure/6JW0| 6JW0]], [[https://www.rcsb.org/structure/6JW1|6JW1]], [[https://www.rcsb.org/structure/6JW2|6JW2]], [[https://www.rcsb.org/structure/6JW3|6JW3]], [[https://www.rcsb.org/structure/6JW4|6JW4]], [[https://www.rcsb.org/structure/6JW5|6JW5]] (Liu & Yi, unpublished)+RefSeq ID: [[https://www.ncbi.nlm.nih.gov/protein/WP_011052943.1|WP_011052943.1]] (1126 aa)\\ 
 +3D structure: [[https://www.rcsb.org/structure/2KQ5|2KQ5]] (Murakami //et al.//, 2010); [[https://www.rcsb.org/structure/3V6P|3V6P]], [[https://www.rcsb.org/structure/3V6T| 3V6T ]] (Deng //et al.//, 2012a); [[https://www.rcsb.org/structure/4GJP|4GJP]], [[https://www.rcsb.org/structure/4GJR|4GJR]] (Deng //et al.//, 2012b); [[https://www.rcsb.org/structure/4HPZ|4HPZ]] (Gao //et al.//, 2012); [[https://www.rcsb.org/structure/3UGM|3UGM]] (Mak //et al.//, 2012); [[https://www.rcsb.org/structure/4GG4|4GG4]] (Yin //et al.//, 2012); [[https://www.rcsb.org/structure/2YPF|2YPF ]] (Stella //et al//., 2013); [[https://www.rcsb.org/structure/4OSH|4OSH]], [[https://www.rcsb.org/structure/4OSI| 4OSI]], [[https://www.rcsb.org/structure/4OSJ| 4OSJ]], [[https://www.rcsb.org/structure/4OSK| 4OSK]], [[https://www.rcsb.org/structure/4OSL| 4OSL]], [[https://www.rcsb.org/structure/4OSM| 4OSM]], [[https://www.rcsb.org/structure/4OSQ|4OSQ]], [[https://www.rcsb.org/structure/4OSR|4OSR]], [[https://www.rcsb.org/structure/4OSS|4OSS]], [[https://www.rcsb.org/structure/4OST| 4OST]], [[https://www.rcsb.org/structure/4OSV| 4OSV]], [[https://www.rcsb.org/structure/4OSW| 4OSW]], [[https://www.rcsb.org/structure/4OSZ| 4OSZ]], [[https://www.rcsb.org/structure/4OT0| 4OT0]], [[https://www.rcsb.org/structure/4OT3| 4OT3]], [[https://www.rcsb.org/structure/4OTO|4OTO]] (Deng //et al.//, 2014); [[https://www.rcsb.org/structure/6JTQ|6JTQ]], [[https://www.rcsb.org/structure/6JVZ|6JVZ]], [[https://www.rcsb.org/structure/6JW0| 6JW0]], [[https://www.rcsb.org/structure/6JW1|6JW1]], [[https://www.rcsb.org/structure/6JW2|6JW2]], [[https://www.rcsb.org/structure/6JW3|6JW3]], [[https://www.rcsb.org/structure/6JW4|6JW4]], [[https://www.rcsb.org/structure/6JW5|6JW5]] (Liu //et al.//2020); [[https://www.rcsb.org/structure/6LEW|6LEW]] (unpublished)
  
 ===== Biological function ===== ===== Biological function =====
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 === How discovered? === === How discovered? ===
  
-The gene //avrBs3 //was cloned in 1989 and was the first gene described of the TAL effector (TALE) family (Minsavage //et al//., 1990). Different resistant and susceptible cultivars of peppers were inoculated with //Xcv// strains 71-21 and 82-8 (Bonas //et al//., 1989). The pepper cultivar ECW-30R carries the resistance gene //Bs3 //and inoculation of these //Xcv// strains provoked a hypersensitive response (HR) (Bonas //et al//., 1989). This indicated that both //Xcv// strains contained //avrBs3//.+The gene //avrBs3// was cloned in 1989 and was the first gene described of the TAL effector (TALE) family (Minsavage //et al//., 1990). Different resistant and susceptible cultivars of peppers were inoculated with //Xcv// strains 71-21 and 82-8 (Bonas //et al//., 1989). The pepper cultivar ECW-30R carries the resistance gene //Bs3// and inoculation of these //Xcv// strains provoked a hypersensitive response (HR) (Bonas //et al//., 1989). This indicated that both //Xcv// strains contained //avrBs3//.
 === (Experimental) evidence for being a T3E === === (Experimental) evidence for being a T3E ===
  
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 === Regulation === === Regulation ===
  
-Unlike most other type III effectors, expression of //avrBs3// is not dependend on the hrp regulon and the gene does not contain a PIP box in its promoter region. It is expressed constitutively in cells grown in minimal or complex medium and in planta (Knoop //et al//., 1991).+Unlike most other type III effectors, expression of //avrBs3// is not dependend on the hrp regulon and the gene does not contain a PIP box in its promoter region. It is expressed constitutively in cells grown in minimal or complex medium and //in planta// (Knoop //et al//., 1991).
 === Phenotypes === === Phenotypes ===
  
 AvrBs3, as well as other members of the TALE family, function as specific transcription factors in plant cells. These proteins bind to specific sequences in promoters and induce expression of downstream genes. The DNA-binding specificity is encoded in the order of individual 34-amino acid repeats which each recognize one DNA base. Different TALEs typically contain different repeats and accordingly bind to different DNA sequences and target different host genes. The contributions of individual TALEs to virulence can thus be quite diverse. AvrBs3, as well as other members of the TALE family, function as specific transcription factors in plant cells. These proteins bind to specific sequences in promoters and induce expression of downstream genes. The DNA-binding specificity is encoded in the order of individual 34-amino acid repeats which each recognize one DNA base. Different TALEs typically contain different repeats and accordingly bind to different DNA sequences and target different host genes. The contributions of individual TALEs to virulence can thus be quite diverse.
  
-Expression analysis using gene promoter fusion and western blot analysis demonstrated that //avrBs3// was expressed and resulted in a 122 kDa protein (1164 aa) which was detectable using a specific polyclonal antibody (Bonas //et al//., 1989). The AvrBs3 effector protein elicits two different types of responses in resistant or susceptible plants. In susceptible pepper plants (Early Cal Wonder; ECW), hypertrophy (i.e. enlargement of mesophyll cells) is triggered by AvrBs3 (Bonas //et al//., 1989; Bonas //et al//., 1991; Marois //et al//., 2002). //Agrobacterium// strains carrying a vector with //avrBs3// induced pustules (hypertrophy) 4-5 dpi in various solanaceous plants including //Nicotiana// //clevelandii//, //N.// //benthamiana//, //N.// //tabacum//, //Petunia hybrida//, //Physalis alkekengi//, //Solanum americanum// and potato (//S.// //tuberosum//), whereas //Agrobacterium// strains carrying an empty vector did not cause any changes in inoculated plants (Marois //et al//., 2002; Kay //et al//., 2007). Differential cDNA analysis from susceptible pepper plants infected with //Xcv// with or without AvrBs3 led to the discovery of //upa// (upregulated by AvrBs3) genes whose expression is induced by AvrBs3 (Marois //et al.//, 2002; Kay //et al//., 2007). These //upa// genes all share a conserved promoter element, known as the //UPA// box (Kay //et al.//, 2007). //upa20// acts as a master regulator of cell enlargement causing the hypertrophy symptoms associated with AvrBs3. Silencing of //upa20// decreased cell hypertrophy in infected plants while the expression of //upa20// led to hypertrophy in uninfected plants (Kay //et al//., 2007).+Expression analysis using gene promoter fusion and western blot analysis demonstrated that //avrBs3// was expressed and resulted in a 122 kDa protein (1164 aa) which was detectable using a specific polyclonal antibody (Bonas //et al//., 1989). The AvrBs3 effector protein elicits two different types of responses in resistant or susceptible plants. In susceptible pepper plants (Early Cal Wonder; ECW), hypertrophy (i.e. enlargement of mesophyll cells) is triggered by AvrBs3 (Bonas //et al//., 1989; Bonas //et al//., 1991; Marois //et al//., 2002). //Agrobacterium// strains carrying a vector with //avrBs3// induced pustules (hypertrophy) 4-5 dpi in various solanaceous plants including //Nicotiana// //clevelandii//, //N.// //benthamiana//, //N.// //tabacum//, //Petunia hybrida//, //Physalis alkekengi//, //Solanum americanum// and potato (//S.// //tuberosum//), whereas //Agrobacterium// strains carrying an empty vector did not cause any changes in inoculated plants (Marois //et al//., 2002; Kay //et al//., 2007). Differential cDNA analysis from susceptible pepper plants infected with //Xcv// with or without AvrBs3 led to the discovery of //upa// (upregulated by AvrBs3) genes whose expression is induced by AvrBs3 (Marois //et al.//, 2002; Kay //et al//., 2007). These //UPA// genes all share a conserved promoter element, known as the //UPA// box (Kay //et al.//, 2007). //UPA20// acts as a master regulator of cell enlargement causing the hypertrophy symptoms associated with AvrBs3. Silencing of //UPA20// decreased cell hypertrophy in infected plants while the expression of //UPA20// led to hypertrophy in uninfected plants (Kay //et al//., 2007).
  
 In resistant pepper plants, the promoter of //Bs3// contains a //UPA// box that is bound by AvrBs3 resulting in the transcription of the gene //Bs3//. //Bs3// encodes a protein that is homologous to flavine-dependent mono-oxygenases (Römer //et al//., 2007) and its expression causes rapid cell death thus preventing the spread of the pathogen (Bonas //et al//., 1989; Bonas //et al//., 1991). In resistant pepper plants, the promoter of //Bs3// contains a //UPA// box that is bound by AvrBs3 resulting in the transcription of the gene //Bs3//. //Bs3// encodes a protein that is homologous to flavine-dependent mono-oxygenases (Römer //et al//., 2007) and its expression causes rapid cell death thus preventing the spread of the pathogen (Bonas //et al//., 1989; Bonas //et al//., 1991).
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 === In other plant pathogens/symbionts === === In other plant pathogens/symbionts ===
  
-Yes: Genes homologous to //avrBs3// of //Xanthomonas// were detected in some strains of //Ralstonia solanacearum// biovars 3, 4 and 5 (Heuer //et al//., 2007), in endofungal strains of //Burkholderia rhizoxinica // (Lacker //et al//., 2011), and in unknown marine organisms. All these related proteins can bind DNA (de Lange //et al//., 2013; de Lange //et al.//, 2014; de Lange //et al//., 2015).+Yes: Genes homologous to //avrBs3// of //Xanthomonas// were detected in some strains of //Ralstonia solanacearum// biovars 3, 4 and 5 (Heuer //et al//., 2007), in endofungal strains of //Burkholderia rhizoxinica// (Lacker //et al//., 2011), and in unknown marine organisms. All these related proteins can bind DNA (de Lange //et al//., 2013; de Lange //et al.//, 2014; de Lange //et al//., 2015).
 ===== References ===== ===== References =====
  
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 de Lange O, Schreiber T, Schandry N, Radeck J, Braun KH, Koszinowski J, Heuer H, Strauß A, Lahaye T (2013). Breaking the DNA-binding code of //Ralstonia solanacearum// TAL effectors provides new possibilities to generate plant resistance genes against bacterial wilt disease. New Phytol. 199: 773-786. DOI: [[https://doi.org/10.1111/nph.12324|10.1111/nph.12324]] de Lange O, Schreiber T, Schandry N, Radeck J, Braun KH, Koszinowski J, Heuer H, Strauß A, Lahaye T (2013). Breaking the DNA-binding code of //Ralstonia solanacearum// TAL effectors provides new possibilities to generate plant resistance genes against bacterial wilt disease. New Phytol. 199: 773-786. DOI: [[https://doi.org/10.1111/nph.12324|10.1111/nph.12324]]
  
-de Lange O, Wolf C, Dietze J, Elsaesser J, Morbitzer R, Lahaye T (2014). Programmable DNA-binding proteins from Burkholderia provide a fresh perspective on the TALE-like repeat domain. Nuc. Acids Res. 42: 7436-7449. DOI: [[https://doi.org/10.1093/nar/gku329.|10.1093/nar/gku329.]]+de Lange O, Wolf C, Dietze J, Elsaesser J, Morbitzer R, Lahaye T (2014). Programmable DNA-binding proteins from Burkholderia provide a fresh perspective on the TALE-like repeat domain. Nuc. Acids Res. 42: 7436-7449. DOI: [[https://doi.org/10.1093/nar/gku329|1093/nar/gku329]]
  
 de Lange O, Wolf C, Thiel P, Krüger J, Kleusch C, Kohlbacher O, Lahaye T (2015). DNA-binding proteins from marine bacteria expand the known sequence diversity of TALE-like repeats. Nuc. Acids Res. 43: 10065-10080. DOI: [[https://doi.org/10.1093/nar/gkv1053|10.1093/nar/gkv1053]] de Lange O, Wolf C, Thiel P, Krüger J, Kleusch C, Kohlbacher O, Lahaye T (2015). DNA-binding proteins from marine bacteria expand the known sequence diversity of TALE-like repeats. Nuc. Acids Res. 43: 10065-10080. DOI: [[https://doi.org/10.1093/nar/gkv1053|10.1093/nar/gkv1053]]
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 Lackner G, Moebius N, Partida-Martinez LP, Boland S, Hertweck C (2011). Evolution of an endofungal lifestyle: Deductions from the //Burkholderia rhizoxinica// genome. BMC Genomics 12: 210. DOI: [[https://doi.org/10.1186/1471-2164-12-210|10.1186/1471-2164-12-210]] Lackner G, Moebius N, Partida-Martinez LP, Boland S, Hertweck C (2011). Evolution of an endofungal lifestyle: Deductions from the //Burkholderia rhizoxinica// genome. BMC Genomics 12: 210. DOI: [[https://doi.org/10.1186/1471-2164-12-210|10.1186/1471-2164-12-210]]
 +
 +Liu L, Zhang Y, Liu M, Wei W, Yi C, Peng J (2020). Structural insights into the specific recognition of 5-methylcytosine and 5-hydroxymethylcytosine by TAL effectors. J. Mol. Biol. 432:1035-1047. doi: [[https://doi.org/10.1016/j.jmb.2019.11.023|10.1016/j.jmb.2019.11.023]]
  
 Mak AN, Bradley P, Cernadas RA, Bogdanove AJ, Stoddard BL (2012). The crystal structure of TAL effector PthXo1 bound to its DNA target. Science 335: 716-719. DOI: [[https://doi.org/10.1126/science.1216211|10.1126/science.1216211]] Mak AN, Bradley P, Cernadas RA, Bogdanove AJ, Stoddard BL (2012). The crystal structure of TAL effector PthXo1 bound to its DNA target. Science 335: 716-719. DOI: [[https://doi.org/10.1126/science.1216211|10.1126/science.1216211]]
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 Stella S, Molina R, Yefimenko I, Prieto J, Silva G, Bertonati C, Juillerat A, Duchateau P, Montoya G (2013). Structure of the AvrBs3–DNA complex provides new insights into the initial thymine-recognition mechanism. Acta Cryst. 69: 1707-1716. DOI: [[http://dx.doi.org/10.1107/S0907444913016429|10.1107/S0907444913016429]] Stella S, Molina R, Yefimenko I, Prieto J, Silva G, Bertonati C, Juillerat A, Duchateau P, Montoya G (2013). Structure of the AvrBs3–DNA complex provides new insights into the initial thymine-recognition mechanism. Acta Cryst. 69: 1707-1716. DOI: [[http://dx.doi.org/10.1107/S0907444913016429|10.1107/S0907444913016429]]
  
-Szurek B, Marois E, Bonas U, Van den Ackerveken G (2001). Eukaryotic features of the //Xanthomonas// type III effector AvrBs3: protein domains involved in transcriptional activation and the interaction with nuclear import receptors from pepper. Plant J. 26: 523-534. DOI: [[https://10.1046/j.0960-7412.2001.01046.x|10.1046/j.0960-7412.2001.01046.x]]+Szurek B, Marois E, Bonas U, Van den Ackerveken G (2001). Eukaryotic features of the //Xanthomonas// type III effector AvrBs3: protein domains involved in transcriptional activation and the interaction with nuclear import receptors from pepper. Plant J. 26: 523-534. DOI: [[https://doi.org/10.1046/j.0960-7412.2001.01046.x|https://doi.org/10.1046/j.0960-7412.2001.01046.x]]
  
 Szurek B, Rossier O, Hause G, Bonas U (2002). Type III-dependent translocation of the //Xanthomonas// AvrBs3 protein into the plant cell. Mol. Microbiol. 46: 13-23. DOI: [[https://doi.org/10.1046/j.1365-2958.2002.03139.x|10.1046/j.1365-2958.2002.03139.x]] Szurek B, Rossier O, Hause G, Bonas U (2002). Type III-dependent translocation of the //Xanthomonas// AvrBs3 protein into the plant cell. Mol. Microbiol. 46: 13-23. DOI: [[https://doi.org/10.1046/j.1365-2958.2002.03139.x|10.1046/j.1365-2958.2002.03139.x]]
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 Van den Ackerveken G, Marois E, Bonas U (1996). Recognition of the bacterial avirulence protein AvrBs3 occurs inside the host plant cell. Cell 87: 1307-1316. DOI: [[https://doi.org/10.1016/S0092-8674(00)81825-5|10.1016/S0092-8674(00)81825-5]] Van den Ackerveken G, Marois E, Bonas U (1996). Recognition of the bacterial avirulence protein AvrBs3 occurs inside the host plant cell. Cell 87: 1307-1316. DOI: [[https://doi.org/10.1016/S0092-8674(00)81825-5|10.1016/S0092-8674(00)81825-5]]
  
-Yin P, Deng D, Yan C, Pan X, Xi JJ, Yan N, Shi Y (2012). Specific DNA-RNA hybrid recognition by TAL effectors. Cell Rep. 2: 707-713. DOI: 1[[https://doi.org/0.1016/j.celrep.2012.09.001|0.1016/j.celrep.2012.09.001]]+Yin P, Deng D, Yan C, Pan X, Xi JJ, Yan N, Shi Y (2012). Specific DNA-RNA hybrid recognition by TAL effectors. Cell Rep. 2: 707-713. DOI: [[https://doi.org/10.1016/j.celrep.2012.09.001|https://doi.org/10.1016/j.celrep.2012.09.001]]
  
 ===== Further reading ===== ===== Further reading =====
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 Xue J, Lu Z, Liu W, Wang S, Lu D, Wang X, He X (2020). The genetic arms race between plant and //Xanthomonas//: lessons learned from TALE biology. Sci. China Life Sci. 63. DOI: [[https://doi.org/10.1007/s11427-020-1699-4|10.1007/s11427-020-1699-4]] Xue J, Lu Z, Liu W, Wang S, Lu D, Wang X, He X (2020). The genetic arms race between plant and //Xanthomonas//: lessons learned from TALE biology. Sci. China Life Sci. 63. DOI: [[https://doi.org/10.1007/s11427-020-1699-4|10.1007/s11427-020-1699-4]]
 +
 +Zhang B, Han X, Yuan W, Zhang H (2022). TALEs as double-edged swords in plant-pathogen interactions: Progress, challenges, and perspectives. Plant. Commun. 3: 100318. DOI: [[https://doi.org/10.1016/j.xplc.2022.100318|10.1016/j.xplc.2022.100318]]
  
 Zhang J, Yin Z, White F (2015). TAL effectors and the executor //R// genes. Front. Plant Sci. 6: 641. DOI: [[https://doi.org/10.3389/fpls.2015.00641|10.3389/fpls.2015.00641]] Zhang J, Yin Z, White F (2015). TAL effectors and the executor //R// genes. Front. Plant Sci. 6: 641. DOI: [[https://doi.org/10.3389/fpls.2015.00641|10.3389/fpls.2015.00641]]
 +
 +===== Acknowledgements =====
 +
 +This fact sheet is based upon work from COST Action CA16107 EuroXanth, supported by COST (European Cooperation in Science and Technology).
  
bacteria/t3e/avrbs3.1598522434.txt.gz · Last modified: 2023/01/09 10:20 (external edit)