BAK1 and BKK1 in Arabidopsis thaliana confer reduced susceptibility to turnip crinkle virus

European Journal of Plant Pathology

Volumn 127, Issue 1, 2010, Pages 149-156

  Yang, Hui ^a,b   Gou, Xiaoping ^b,c   He, Kai ^b   Xi, Dehui ^a   Du, Junbo ^a   Lin, Honghui ^a   Li, Jia ^b,c  

^a SICHUAN UNIVERSITY   (China)

^b UNIVERSITY OF OKLAHOMA   (United States)

^c LANZHOU UNIVERSITY   (China)

Author keywords

BAK1; BKK1; Cell death; Susceptible; Turnip crinkle virus (TCV)

Indexed keywords

BACTERIUM; BIOLOGICAL CONTROL; DICOTYLEDON; FUNGUS; GENE EXPRESSION; INFECTIOUS DISEASE; VIRUS;

ARABIDOPSIS; ARABIDOPSIS THALIANA; BACTERIA (MICROORGANISMS); BRASSICA RAPA SUBSP. RAPA; FUNGI; TURNIP CRINKLE VIRUS;

EID: 77950020800     PISSN: 09291873     EISSN: None     Source Type: Journal    
DOI: 10.1007/s10658-010-9581-5     Document Type: Article

References (29)

1. Carrington, J. C., Heaton, L. A., Zuidema, D., Hillman, B. I., & Morris, T. J. (1989). The genome structure of Turnip crinkle virus. Virology, 170, 219-226.
2. Chinchilla, D., Zipfel, C., Robatzek, S., Kemmerling, B., Nurnberger, T., Jones, J. D., et al. (2007). A flagellin-induced complex of the receptor FLS2 and BAK1 initiates plant defence. Nature, 448, 497-500. doi: 10. 1038/nature05999.
3. Chisholm, S. T., Coaker, G., Day, B., & Staskawicz, B. J. (2006). Host-microbe interactions: shaping the evolution of the plant immune response. Cell, 124, 803-814. doi: 10. 1016/j. cell. 2006. 02. 008.
4. Cooley, M. B., Pathirana, S., Wu, H. J., Kachroo, P., & Klessig, D. F. (2000). Members of the Arabidopsis HRT/RPP8 family of resistance genes confer resistance to both viral and oomycete pathogens. Plant Cell, 12, 663-676. doi: 10. 1105/tpc. 12. 5. 663.
5. Feys, B. J., & Parker, J. E. (2000). Interplay of signalling pathways in plant disease resistance. Trends in Genetics, 16, 449-455. doi: 10. 1016/S0168-9525(00)02107-7.
6. Greenberg, J. T., & Yao, N. (2004). The role and regulation of programmed cell death in plant-pathogen interactions. Cellular Microbiology, 6, 201-211. doi: 10. 1111/j. 1462-5822. 2004. 00361. x.
7. Greenberg, J. T., Silverman, F. P., & Liang, H. (2000). Uncoupling salicylic acid-dependent cell death and defense-related responses from disease resistance in the Arabidopsis mutant acd5. Genetics, 156, 341-350.
8. He, K., Gou, X., Yuan, T., Lin, H., Asami, T., Yoshida, S., et al. (2007). BAK1 and BKK1 regulate brassinosteroid-dependent growth and brassinosteroid-independent cell-death pathways. Current Biology, 17, 1109-1115. doi: 10. 1016/j. cub. 2007. 05. 036.
9. Heath, M. C. (1998). Apoptosis, programmed cell death and the hypersensitive response. European Journal of Plant Pathology, 104, 117-124. doi: 10. 1023/A: 1008645520976.
10. Heath, M. C. (2000). Hypersensitive response-related death. Plant Molecular Biology, 44, 321-334. doi: 10. 1023/A: 1026592509060.
11. Hecht, V., Vielle-Calzada, J. P., Hartog, M. V., Schmidt, E. D., Boutilier, K., Grossniklaus, U., et al. (2001). The Arabidopsis SOMATIC EMBRYOGENESIS RECEPTOR KINASE 1 gene is expressed in developing ovules and embryos and enhances embryogenic competence in culture. Plant Physiology, 127, 803-816. doi: 10. 1104/pp. 010324.
12. Heese, A., Hann, D. R., Gimenez-Ibanez, S., Jones, A. M., He, K., Li, J., et al. (2007). The receptor-like kinase SERK3/BAK1 is a central regulator of innate immunity in plants. Proceedings of the National Academy of Sciences of the United States of America, 104, 12217-12222. doi: 10. 1073/pnas. 0705306104.
13. Kachroo, P., Yoshioka, K., Shah, J., Dooner, H. K., & Klessig, D. F. (2000). Resistance to Turnip crinkle virus in Arabidopsis is regulated by two host genes and is salicylic acid dependent but NPR1, ethylene, and jasmonate independent. Plant Cell, 12, 677-690. doi: 10. 1105/tpc. 12. 5. 677.
14. Kemmerling, B., Schwedt, A., Rodriguez, P., Mazzotta, S., Frank, M., Qamar, S. A., et al. (2007). The BRI1-associated kinase 1, BAK1, has a brassinolide-independent role in plant cell-death control. Current Biology, 17, 1116-1122. doi: 10. 1016/j. cub. 2007. 05. 046.
15. Lam, E. (2004). Controlled cell death, plant survival and development. Nature Reviews. Molecular Cell Biology, 5, 305-315. doi: 10. 1038/nrm1358.
16. Li, J., Wen, J., Lease, K. A., Doke, J. T., Tax, F. E., & Walker, J. C. (2002). BAK1, an Arabidopsis LRR receptor-like protein kinase, interacts with BRI1 and modulates brassinosteroid signaling. Cell, 110, 213-222. doi: 10. 1016/S0092-8674(02)00812-7.
17. Lucas, W. J. (1995). Plasmodesmata: Intercellular channels for macromolecular transport in plants. Current Opinion in Cell Biology, 7, 673-680. doi: 10. 1016/0955-0674(95)80109-X.
18. Nakashita, H., Yasuda, M., Nitta, T., Asami, T., Fujioka, S., Arai, Y., et al. (2003). Brassinosteroid functions in a broad range of disease resistance in tobacco and rice. Plant Journal, 33, 887-898. doi: 10. 1046/j. 1365-313X. 2003. 01675. x.
19. Nam, K. H., & Li, J. (2002). BRI1/BAK1, a receptor kinase pair mediating brassinosteroid signaling. Cell, 110, 203-212. doi: 10. 1016/S0092-8674(02)00814-0.
20. Opalka, N., Brugidou, C., Bonneau, C., Nicole, M., Beachy, R. N., Yeager, M., et al. (1998). Movement of rice yellow mottle virus between xylem cells through pit membranes. Proceedings of the National Academy of Sciences of the United States of America, 95, 3323-3328.
21. Penninckx, I. A., Eggermont, K., Terras, F. R., Thomma, B. P., Samblanx, G. W., Buchala, A., et al. (1996). Pathogen-induced systemic activation of a plant defensin gene in Arabidopsis follows a salicylic acid-independent pathway. Plant Cell, 8, 2309-2323.
22. Pilloff, R. K., Devadas, S. K., Enyedi, A., & Raina, R. (2002). The Arabidopsis gain-of-function mutant dll1 spontaneously develops lesions mimicking cell death associated with disease. Plant Journal, 30, 61-70. doi: 10. 1046/j. 1365-313X. 2002. 01265. x.
23. Shan, L., He, P., Li, J., Heese, A., Peck, S. C., Nurnberger, T., et al. (2008). Bacterial effectors target the common signaling partner BAK1 to disrupt multiple MAMP receptor-signaling complexes and impede plant immunity. Cell Host & Microbe, 4, 17-27. doi: 10. 1016/j. chom. 2008. 05. 017.
24. Uknes, S., Mauch-Mani, B., Moyer, M., Potter, S., Williams, S., Dincher, S., et al. (1992). Acquired resistance in Arabidopsis. Plant Cell, 4, 645-656.
25. Wang, Y., Gaba, V., Yang, J., Palukaitis, P., & Gal-On, A. (2002). Characterization of Synergy Between Cucumber mosaic virus and Potyviruses in Cucurbit Hosts. Phytopathology, 92, 51-58. doi: 10. 1094/PHYTO. 2002. 92. 1. 51.
26. Whitham, S., Dinesh-Kumar, S. P., Choi, D., Hehl, R., Corr, C., & Baker, B. (1994). The product of the tobacco mosaic virus resistance gene N: similarity to toll and the interleukin-1 receptor. Cell, 78, 1101-1115. doi: 10. 1016/0092-8674(94)90283-6.
27. Xi, D., Feng, H., Lan, L., Du, J., Wang, J., Zhang, Z., et al. (2007). Characterization of Synergy between Cucumber mosaic virus and Tobacco necrosis virus in Nicotiana benthamiana. Journal of Phytopathology, 155, 570-573. doi: 10. 1111/j. 1439-0434. 2007. 01279. x.
28. Yao, N., Imai, S., Tada, Y., Nakayashiki, H., Tosa, Y., Park, P., et al. (2002). Apoptotic Cell Death is a Common Response to pathogen Attack in Oats. Molecular Plant-Microbe Interactions, 15, 1000-1007. doi: 10. 1094/MPMI. 2002. 15. 10. 1000.
29. Zipfel, C., Kunze, G., Chinchilla, D., Caniard, A., Jones, J. D., Boller, T., et al. (2006). Perception of the bacterial PAMP EF-Tu by the receptor EFR restricts Agrobacterium-mediated transformation. Cell, 125, 749-760. doi: 10. 1016/j. cell. 2006. 03. 037.