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bacteria:t3e:xopj5

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bacteria:t3e:xopj5 [2020/07/03 17:24]
rkoebnik
bacteria:t3e:xopj5 [2020/08/09 18:11] (current)
rkoebnik [Biological function]
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 Expert reviewer: FIXME Expert reviewer: FIXME
  
-Class: yopJ\\ +Class: XopJ\\ 
-Family: yopJ\\ +Family: XopJ5\\ 
-Prototype: avrXccB (//Xanthomonas campestris// pv. //campestris// strain ATCC 33913)\\+Prototype: AvrXccB (//Xanthomonas campestris// pv. //campestris//strain ATCC 33913)\\
 RefSeq ID: [[https://www.ncbi.nlm.nih.gov/protein/NP_639077|NP_639077]] (235 aa)\\ RefSeq ID: [[https://www.ncbi.nlm.nih.gov/protein/NP_639077|NP_639077]] (235 aa)\\
 +Synonym: AvrXccB\\
 3D structure: Unknown 3D structure: Unknown
  
 ===== Biological function ===== ===== Biological function =====
  
-In //Arabidopsis//, AvrXccB (AKA XopJ5) targets putative S- adenosyl-L-methionine-dependent methyltransferase (SAM-MT) (Liu //et al//., 2017).+In //Arabidopsis//, AvrXccB (aka XopJ5) targets putative S- adenosyl-L-methionine-dependent methyltransferase (SAM-MT) (Liu //et al//., 2017).
 === How discovered? === === How discovered? ===
  
-Original discovery was through bioinformatic predictions and comparative genomics of //Xanthomonas axonopodis// pv. //citri// (//Xac//) and //Xanthomonas campestris// pv. //campestris// (//Xcc//) (da Silva //et al//., 2002). XopJ5 (AvrXccB) was also identified in //X. campestris// pv. //campestris// (//Xcc//strain 8004 as a candidate T3E due to the presence of a plant-inducible promoter (PIP) box in its gene, XC_3802 (Jiang //et al.//, 2009).+Original discovery was through bioinformatic predictions and comparative genomics of //Xanthomonas axonopodis// pv. //citri// (//Xac//) and //Xanthomonas campestris// pv. //campestris// (//Xcc//) (da Silva //et al//., 2002). XopJ5 (AvrXccB) was also identified in //Xcc// strain 8004 as a candidate T3E due to the presence of a plant-inducible promoter (PIP) box in its gene, XC_3802 (Jiang //et al.//, 2009).
 === (Experimental) evidence for being a T3E === === (Experimental) evidence for being a T3E ===
  
-T3E-defective mutant was not capable of secreting the effector protein when carrying the plasmid-borne gene encoding for AvrXccB. +AvrXccB, fused to a HA tag, was shown to be secreted into culture supernatants by Western blot analysis using an anti‐haemagglutinin (HA) antibody. In contrast, a T3E-defective mutant was not capable of secreting this effector (Liu //et al//., 2017).
 === Regulation === === Regulation ===
  
-HrpG and HrpX (Jiang //et al//., 2009; Rongqi //et al//., 2006).+The //xopE1// <sub>Xcc8004</sub> gene (//avrXccB//) contains a PIP box and was shown to be controlled by //hrpG// and //hrpX// (Rongqi //et al//., 2006; Jiang et al., 2009).
 === Phenotypes === === Phenotypes ===
  
-AvrXccB is not essential for full virulence of //Xcc// in host Chinese radish. Experimental evidence using heterologous expression of //avrXccB// suggests that this protein is involved in the suppression of plant immunity. Immunity suppression in //Arabidopsis// involved multiple mechanisms: ectopic expression of //avrXccB// reduced flg22-induced callose deposition and ROS production, while //avrXccB// expression in //Arabidopsis// protoplasts inhibited the promoter activity of resistance gene //NHO1//. Heterologous expression of //avrXccB// led to an increase in the in-planta population of //Xcc// B186 and //Pst// DC300 in //Arabidopsis//. Conversely, //avrXccB// mutants were compromised in their ability to inhibit MAMP-induced immunity (callose deposition, ROS production and defence-related genes in //Arabidopsis// protoplasts) (Liu //et al//., 2017).+  * AvrXccB (XopJ5<sub>Xcc8004</sub>is not required for full virulence and growth of //Xcc//  in the host plant Chinese radish (Jiang //et al.//, 2009). 
 +  * XopJ5 was found to be associated with variations in disease symptoms when testing a set of 45 //X. campestris //pv. //campestris //strains on two //Arabidopsis//  natural accessions (Guy //et al.//, 2013). 
 +  * Experimental evidence using heterologous expression of //avrXccB//  suggests that this protein is involved in the suppression of plant immunity. Immunity suppression in //Arabidopsis//  involved multiple mechanisms: ectopic expression of //avrXccB//  reduced flg22-induced callose deposition and ROS production, while //avrXccB//  expression in //Arabidopsis//  protoplasts inhibited the promoter activity of resistance gene //NHO1//. Heterologous expression of //avrXccB//  led to an increase in the in-planta population of //Xcc//  B186 and //Pst//  DC300 in //Arabidopsis//. Conversely, //avrXccB//  mutants were compromised in their ability to inhibit MAMP-induced immunity (callose deposition, ROS production and defence-related genes in //Arabidopsis//  protoplasts) (Liu //et al//., 2017). 
 === Localization === === Localization ===
  
-Membrane, confirmed experimentally through GFP-tagged AvrXccB expression in transgenic //Arabidopsis// (Liu //et al//., 2017Thieme //et al//., 2007)+Plant plasma membrane, confirmed experimentally through GFP-tagged AvrXccB expression in transgenic //Arabidopsis//. The putative //N//  ‐myristoylation motif is essential for its localization (Thieme //et al//., 2007Liu //et al//., 2017)
 === Enzymatic function === === Enzymatic function ===
  
-Cysteine protease/acetyltransferase (putative) (Liu //et al//., 2017). Point mutations in the catalytic triad (conserved with other YopJ-like proteins which also function as protease/acetyltransferases) compromised //NOH1// promoter activity and were deprived of their abilities to suppress flg22-induced callose deposition and ROS production (Liu //et al//., 2017).+Cysteine protease/acetyltransferase (putative) (Liu //et al//., 2017). Point mutations in the catalytic triad (conserved with other YopJ-like proteins which also function as protease/acetyltransferases) compromised //NOH1//  promoter activity and were deprived of their abilities to suppress flg22-induced callose deposition and ROS production (Liu //et al//., 2017). 
 === Interaction partners === === Interaction partners ===
  
-AvrXccB interacts with SAM-MT1 in //Arabidopsis//through SAM-MT1's C-terminal domain. AvrXccB-SAM-MT1 interaction was determined experimentally using in-vitro pull-down assays and Co-IP assays (Liu //et al//., 2017).+AvrXccB interacts with //S//  ‐adenosyl‐L‐methionine‐dependent methyltransferases SAM‐MT1 and SAM‐MT2 in //Arabidopsis//. Interaction with SAM-MT1 in //Arabidopsis//  occurs through SAM-MT1's C-terminal domain. AvrXccB-SAM-MT1 interaction was determined experimentally using in-vitro pull-down assays and Co-IP assays (Liu //et al//., 2017). 
 ===== Conservation ===== ===== Conservation =====
  
 === In xanthomonads === === In xanthomonads ===
  
-Yes. YopJ-like effectors such as AvrBsT in //Xcv// or //Xcc//, XopJ in //Xcv//.+Yes. YopJ-like effectors such as AvrBsT in //Xcv//  or //Xcc//, XopJ in //Xcv//. 
 === In other plant pathogens/symbionts === === In other plant pathogens/symbionts ===
  
-Yes. YopJ-like effectors HopZ1a in //P. syringae// and Pop2 in //R. solanacearum//.+Yes. YopJ-like effectors HopZ1a in //P. syringae//  and Pop2 in //R. solanacearum//. 
 ===== References ===== ===== References =====
  
-da Silva AC, Ferro JA, Reinach FC, Farah CS, Furlan LR, Quaggio RB, Monteiro-Vitorello CB, Van Sluys MA, Almeida NF, Alves LM, do Amaral AM, Bertolini MC, Camargo LE, Camarotte G, Cannavan F, Cardozo J, Chambergo F, Ciapina LP, Cicarelli RM, Coutinho LL, Cursino-Santos JR, El-Dorry H, Faria JB, Ferreira AJ, Ferreira RC, Ferro MI, Formighieri EF, Franco MC, Greggio CC, Gruber A, Katsuyama AM, Kishi LT, Leite RP, Lemos EG, Lemos MV, Locali EC, Machado MA, Madeira AM, Martinez-Rossi NM, Martins EC, Meidanis J, Menck CF, Miyaki CY, Moon DH, Moreira LM, Novo MT, Okura VK, Oliveira MC, Oliveira VR, Pereira HA, Rossi A, Sena JA, Silva C, de Souza RF, Spinola LA, Takita MA, Tamura RE, Teixeira EC, Tezza RI, Trindade dos Santos M, Truffi D, Tsai SM, White FF, Setubal JC, Kitajima JP (2002). Comparison of the genomes of two //Xanthomonas// pathogens with differing host specificities. Nature 417: 459-463. DOI: [[https://doi.org/10.1038/417459a|10.1038/417459a]]+da Silva AC, Ferro JA, Reinach FC, Farah CS, Furlan LR, Quaggio RB, Monteiro-Vitorello CB, Van Sluys MA, Almeida NF, Alves LM, do Amaral AM, Bertolini MC, Camargo LE, Camarotte G, Cannavan F, Cardozo J, Chambergo F, Ciapina LP, Cicarelli RM, Coutinho LL, Cursino-Santos JR, El-Dorry H, Faria JB, Ferreira AJ, Ferreira RC, Ferro MI, Formighieri EF, Franco MC, Greggio CC, Gruber A, Katsuyama AM, Kishi LT, Leite RP, Lemos EG, Lemos MV, Locali EC, Machado MA, Madeira AM, Martinez-Rossi NM, Martins EC, Meidanis J, Menck CF, Miyaki CY, Moon DH, Moreira LM, Novo MT, Okura VK, Oliveira MC, Oliveira VR, Pereira HA, Rossi A, Sena JA, Silva C, de Souza RF, Spinola LA, Takita MA, Tamura RE, Teixeira EC, Tezza RI, Trindade dos Santos M, Truffi D, Tsai SM, White FF, Setubal JC, Kitajima JP (2002). Comparison of the genomes of two //Xanthomonas//  pathogens with differing host specificities. Nature 417: 459-463. DOI: [[https://doi.org/10.1038/417459a|10.1038/417459a]] 
 + 
 +Guy E, Genissel A, Hajri A, Chabannes M, David P, Carrere S, Lautier M, Roux B, Boureau T, Arlat M, Poussier S, Noël LD (2013). Natural genetic variation of //Xanthomonas campestris//  pv. //campestris//  pathogenicity on //Arabidopsis//  revealed by association and reverse genetics. mBio 4: e00538-12. DOI: [[https://doi.org/10.1128/mBio.00538-12|10.1128/mBio.00538-12]]. Erratum in: MBio (2013) 4: e00978-13.
  
-Jiang W, Jiang BL, Xu RQ, Huang JD, Wei HY, Jiang GF, Cen WJ, Liu J, Ge YY, Li GH, Su LL, Hang XH, Tang DJ, Lu GT, Feng JX, He YQ, Tang JL (2009). Identification of six type III effector genes with the PIP box in //Xanthomonas campestris// pv. //campestris// and five of them contribute individually to full pathogenicity. Mol. Plant Microbe Interact. 22: 1401-1411. DOI: [[https://doi.org/10.1094/mpmi-22-11-1401|10.1094/mpmi-22-11-1401]]+Jiang W, Jiang BL, Xu RQ, Huang JD, Wei HY, Jiang GF, Cen WJ, Liu J, Ge YY, Li GH, Su LL, Hang XH, Tang DJ, Lu GT, Feng JX, He YQ, Tang JL (2009). Identification of six type III effector genes with the PIP box in //Xanthomonas campestris//  pv. //campestris//  and five of them contribute individually to full pathogenicity. Mol. Plant Microbe Interact. 22: 1401-1411. DOI: [[https://doi.org/10.1094/mpmi-22-11-1401|10.1094/mpmi-22-11-1401]]
  
-Liu L, Wang Y, Cui F, Fang A, Wang S, Wang J, Wei C, Li S, Sun W (2017). The type III effector AvrXccB in //Xanthomonas campestris// pv. //campestris// targets putative methyltransferases and suppresses innate immunity in //Arabidopsis//. Mol. Plant Pathol. 18: 768-782. DOI: [[https://doi.org/10.1111/mpp.12435|10.1111/mpp.12435]]+Liu L, Wang Y, Cui F, Fang A, Wang S, Wang J, Wei C, Li S, Sun W (2017). The type III effector AvrXccB in //Xanthomonas campestris//  pv. //campestris//  targets putative methyltransferases and suppresses innate immunity in //Arabidopsis//. Mol. Plant Pathol. 18: 768-782. DOI: [[https://doi.org/10.1111/mpp.12435|10.1111/mpp.12435]]
  
-Rongqi X, Xianzhen L, Hongyu W, Bole J, Kai L, Yongqiang H, Jiaxuan F, Jiliang T (2006). Regulation of eight avr by hrpG and hrpX in //Xanthomonas campestris// pv. //campestris// and their role in pathogenicity. Prog. Nat. Sci. 16: 1288-1294. DOI: [[https://doi.org/10.1080/10020070612330143|10.1080/10020070612330143]]+Rongqi X, Xianzhen L, Hongyu W, Bole J, Kai L, Yongqiang H, Jiaxuan F, Jiliang T (2006). Regulation of eight //avr//  by //hrpG//  and //hrpX//  in //Xanthomonas campestris//  pv. //campestris//  and their role in pathogenicity. Prog. Nat. Sci. 16: 1288-1294. DOI: [[https://doi.org/10.1080/10020070612330143|10.1080/10020070612330143]]
  
-Thieme F, Szczesny R, Urban A, Kirchner O, Hause G, Bonas U (2007). New type III effectors from //Xanthomonas campestris// pv. //vesicatoria// trigger plant reactions dependent on a conserved N-myristoylation motif. Mol Plant Microbe Interact. 20: 1250-1261. DOI: [[https://doi.org/10.1094/MPMI-20-10-1250|10.1094/MPMI-20-10-1250]]+Thieme F, Szczesny R, Urban A, Kirchner O, Hause G, Bonas U (2007). New type III effectors from //Xanthomonas campestris//  pv. //vesicatoria//  trigger plant reactions dependent on a conserved N-myristoylation motif. MolPlant Microbe Interact. 20: 1250-1261. DOI: [[https://doi.org/10.1094/MPMI-20-10-1250|10.1094/MPMI-20-10-1250]]
  
bacteria/t3e/xopj5.1593789857.txt.gz · Last modified: 2020/07/03 17:24 by rkoebnik