XA27 Depends on an Amino-Terminal Signal-Anchor-Like Sequence to Localize to the Apoplast for Resistance to Xanthomonas oryzae pv oryzae

被引:42
作者
Wu, Lifang [1 ]
Goh, Mei Ling [1 ]
Sreekala, Chellamma [1 ]
Yin, Zhongchao [1 ]
机构
[1] Natl Univ Singapore, Temasek Life Sci Lab, Singapore 117604, Singapore
关键词
D O I
10.1104/pp.108.123356
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The rice (Oryza sativa) gene Xa27 confers resistance to Xanthomonas oryzae pv oryzae, the causal agent of bacterial blight disease in rice. Sequence analysis of the deduced XA27 protein provides little or no clue to its mode of action, except that a signal-anchor-like sequence is predicted at the amino (N)-terminal region of XA27. As part of an effort to characterize the biochemical function of XA27, we decided to determine its subcellular localization. Initial studies showed that a functional XA27-green fluorescent protein fusion protein accumulated in vascular elements, the host sites where the bacterial blight pathogens multiply. The localization of XA27-green fluorescent protein to the apoplast was verified by detection of the protein on cell walls of leaf sheath and root cells after plasmolysis. Similarly, XA27-FLAG localizes to xylem vessels and cell walls of xylem parenchyma cells, revealed by immunogold electron microscopy. XA27-FLAG could be secreted from electron-dense vesicles in cytoplasm to the apoplast via exocytosis. The signal-anchor-like sequence has an N-terminal positively charged region including a triple arginine motif followed by a hydrophobic region. Deletion of the hydrophobic region or substitution of the triple arginine motif with glycine or lysine residues abolished the localization of the mutated proteins to the cell wall and impaired the plant's resistance to X. oryzae pv oryzae. These results indicate that XA27 depends on the N-terminal signal-anchor-like sequence to localize to the apoplast and that this localization is important for resistance to X. oryzae pv oryzae.
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页码:1497 / 1509
页数:13
相关论文
共 39 条
[1]   Initiation of RPS2-specified disease resistance in Arabidopsis is coupled to the AvrRpt2-directed elimination of RIN4 [J].
Axtell, MJ ;
Staskawicz, BJ .
CELL, 2003, 112 (03) :369-377
[2]   The Rieske protein from Paracoccus denitrificans is inserted into the cytoplasmic membrane by the twin-arginine translocase [J].
Bachmann, Julie ;
Bauer, Brigitte ;
Zwicker, Klaus ;
Ludwig, Bernd ;
Anderka, Oliver .
FEBS JOURNAL, 2006, 273 (21) :4817-4830
[3]   The Arabidopsis thaliana RPM1 disease resistance gene product is a peripheral plasma membrane protein that is degraded coincident with the hypersensitive response [J].
Boyes, DC ;
Nam, J ;
Dangl, JL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (26) :15849-15854
[4]   A novel role for the TIR domain in association with pathogen-derived elicitors [J].
Burch-Smith, Tessa M. ;
Schiff, Michael ;
Caplan, Jeffrey L. ;
Tsao, Jeffrey ;
Czymmek, Kirk ;
Dinesh-Kumar, Savithramma P. .
PLOS BIOLOGY, 2007, 5 (03) :501-514
[5]   Isolation of a gene encoding Arabidopsis membrane-associated acyl-CoA binding protein and immunolocalization of its gene product [J].
Chye, ML ;
Huang, BQ ;
Zee, SY .
PLANT JOURNAL, 1999, 18 (02) :205-214
[6]   Plant pathogens and integrated defence responses to infection [J].
Dangl, JL ;
Jones, JDG .
NATURE, 2001, 411 (6839) :826-833
[7]   Physical interaction between RRS1-R, a protein conferring resistance to bacterial wilt, and PopP2, a type III effector targeted to the plant nucleus [J].
Deslandes, L ;
Olivier, J ;
Peeters, N ;
Feng, DX ;
Khounlotham, M ;
Boucher, C ;
Somssich, I ;
Genin, S ;
Marco, Y .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (13) :8024-8029
[8]  
Dietz KJ, 1997, PROGR BOT, V58, P221, DOI DOI 10.1007/978-3-642-60458-4_9
[9]  
Edreva A., 2005, General and Applied Plant Physiology, V31, P105
[10]   Locating proteins in the cell using TargetP, SignalP and related tools [J].
Emanuelsson, Olof ;
Brunak, Soren ;
von Heijne, Gunnar ;
Nielsen, Henrik .
NATURE PROTOCOLS, 2007, 2 (04) :953-971