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bacteria:t3e:xopy [2020/06/09 16:04] – [References] jfpothier | bacteria:t3e:xopy [2025/02/13 12:59] (current) – jfpothier | ||
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- | ====== XopY ====== | + | ====== |
- | Author: Irena Mačionienė\\ | + | Author: |
- | Internal reviewer: Lucas Morinière\\ | + | Internal reviewer: |
- | Expert reviewer: FIXME | + | |
Class: XopY\\ | Class: XopY\\ | ||
Family: XopY\\ | Family: XopY\\ | ||
- | Prototype: | + | Prototype: |
- | RefSeq ID: [[https:// | + | GenBank ID: [[https:// |
+ | RefSeq ID: [[https:// | ||
+ | 3D structure: Unknown | ||
===== Biological function ===== | ===== Biological function ===== | ||
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=== How discovered? === | === How discovered? === | ||
- | XopY was discovered by screening the genome of //X. oryzae //pv. // | + | XopY was discovered by screening the genome of //X. oryzae// pv. // |
=== (Experimental) evidence for being a T3E === | === (Experimental) evidence for being a T3E === | ||
- | //X. oryzae //pv. //oryzae // | + | //X. oryzae// pv. //oryzae// transformants containing a plasmidic fusion of XopY (= XOO1488) with the Cya translocation reporter system were inoculated in tomato leaves. An increase of cAMP in the inflitrated areas was observed, thus revealing translocation of the fused protein into plant cells (Furutani //et al.//, 2009). |
=== Regulation === | === Regulation === | ||
- | XopY from //X. oryzae //pv. //oryzae// posseses a PIP and ‐10 box in the promoter region (TTCGB‐N< | + | XopY from //X. oryzae// pv. //oryzae// posseses a PIP and ‐10 box in the promoter region (TTCGB‐N< |
+ | |||
+ | qRT-PCR revealed that transcript levels of 15 out of 18 tested non-TAL effector genes (as well as the regulatory genes //hrpG// and //hrpX//), including //xopY//, were significantly reduced in the // | ||
=== Phenotypes === | === Phenotypes === | ||
- | Transgenic rice plants expressing XOO1488 (Xoo1488-OX) were generated and inoculated with the T3SS-deficient //hrpX// mutant of //Xoo//, which is incapable of type III effector delivery. The //Xoo hrpX// mutant did not cause lesions in wild-type plant, presumably because of strong induction of PTI. In contrast, Xoo1488-OX plants had severe disease symptoms following infection with the //Xoo hrpX// mutant. Bacterial populations of the //Xoo hrpX// mutant in Xoo1488-OX leaves were higher than in wild-type plants. The growth of wild-type isolate Xoo MAFF311018 in Xoo1488-OX plants also increased significantly over its growth in wild-type plants. Thus, it is likely that XopY inhibits PTI induced by infection of //Xoo hrpX// mutant. However, it was noted that XopY knockout strain did not exhibit any defect in virulence (Yamaguchi //et al//., 2013a). XopY was also shown to inhibit chitin-induced expression of defense-related genes (Yamaguchi //et al. //2013b). XopY of //X. oryzae //pv. // | + | Transgenic rice plants expressing XOO1488 (Xoo1488-OX) were generated and inoculated with the T3SS-deficient //hrpX// mutant of //Xoo//, which is incapable of type III effector delivery. The //Xoo hrpX// mutant did not cause lesions in wild-type plant, presumably because of strong induction of PTI. In contrast, Xoo1488-OX plants had severe disease symptoms following infection with the //Xoo hrpX// mutant. Bacterial populations of the //Xoo hrpX// mutant in Xoo1488-OX leaves were higher than in wild-type plants. The growth of wild-type isolate |
=== Localization === | === Localization === | ||
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XopY was demonstrated to target OsRLCK185. Expression of XopY in rice cells compromises OsRLCK185-mediated immune responses, which is consistent with the fact that Xoo1488 inhibits trans-phosphorylation of the activation domain of OsRLCK185 by OsCERK1. Interestingly, | XopY was demonstrated to target OsRLCK185. Expression of XopY in rice cells compromises OsRLCK185-mediated immune responses, which is consistent with the fact that Xoo1488 inhibits trans-phosphorylation of the activation domain of OsRLCK185 by OsCERK1. Interestingly, | ||
- | |||
===== Conservation ===== | ===== Conservation ===== | ||
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===== References ===== | ===== References ===== | ||
- | <font 11pt/ | + | Furutani A, Takaoka M, Sanada H, Noguchi Y, Oku T, Tsuno K, Ochiai H, Tsuge S (2009). Identification of novel type III secretion effectors in // |
+ | |||
+ | Li S, Wang Y, Wang S, Fang A, Wang J, Liu L, Zhang K, Mao Y, Sun W (2015). The type III effector AvrBs2 in // | ||
+ | |||
+ | Liu Y, Long J, Shen D, Song C (2016). // | ||
+ | |||
+ | Song C, Yang B (2010). Mutagenesis of 18 type III effectors reveals virulence function of XopZ< | ||
- | <font 11pt/ | + | Yamaguchi K, Nakamura |
- | <font 11pt/Arial,Helvetica,sans-serif;; | + | Yamaguchi K, Yamada K, Ishikawa K, Yoshimura S, Hayashi N, Uchihashi K, Ishihama N, Kishi-Kaboshi M, Takahashi A, Tsuge S, Ochiai H, Tada Y, Shimamoto K, Yoshioka H, Kawasaki T (2013b). A receptor-like cytoplasmic kinase targeted by a plant pathogen effector is directly phosphorylated by the chitin receptor and mediates rice immunity. Cell Host Microbe 13: 347-357. DOI: [[https:// |
- | <font 11pt/ | + | ===== Acknowledgements ===== |
- | <font 11pt/Arial,Helvetica, | + | This fact sheet is based upon work from COST Action CA16107 EuroXanth, supported by COST (European Cooperation in Science and Technology). |