Acknowledgement
Supported by : Ministry of Education, Science and Technology of Korea, Korea Science and Engineering Foundation, Rural Development Administration
References
- Agrawal, G.K., Jwa, N.S., and Rakwal, R. (2000a). A novel rice (Oryza sativa L.) acidic PR1 gene highly responsive to cut, phytohormones, and protein phosphatase inhibitors. Biochem. Biophys. Res. Commun. 274, 157-165 https://doi.org/10.1006/bbrc.2000.3114
- Agrawal, G.K., Rakwal, R., and Jwa, N.S. (2000b). Rice (Oryza sativa L.) OsPR1b gene is phytohormonally regulated in close interaction with light signals. Biochem. Biophys. Res. Commun.278, 290-298 https://doi.org/10.1006/bbrc.2000.3781
- Ali, G.S., Reddy, V.S., Lindgren, P.B., Jakobek, J.L., and Reddy, A.S. (2003). Differential expression of genes encoding calmodulin-binding proteins in response to bacterial pathogens and inducers of defense responses. Plant Mol. Biol. 51, 803-815 https://doi.org/10.1023/A:1023001403794
- Belenghi, B., Acconcia, F., Trovato, M., Perazzolli, M., Bocedi, A., Polticelli, F., Ascenzi, P., and Delledonne, M. (2003). AtCYS1, a cystatin from Arabidopsis thaliana, suppresses hypersensitive cell death. Eur. J. Biochem. 270, 2593-2604 https://doi.org/10.1046/j.1432-1033.2003.03630.x
- Bouche, N., Scharlat, A., Snedden, W., Bouchez, D., and Fromm, H. (2002). A novel family of calmodulin-binding transcription activators in multicellular organisms. J. Biol. Chem. 277, 21851-21861 https://doi.org/10.1074/jbc.M200268200
- Bouche, N., Yellin, A., Snedden, W.A., and Fromm, H. (2005). Plant-specific calmodulin-binding proteins. Annu. Rev. Plant Biol. 56, 435-466 https://doi.org/10.1146/annurev.arplant.56.032604.144224
- Buschges, R., Hollricher, K., Panstruga, R., Simons, G., Wolter, M., Frijters, A., van Daelen, R., van der Lee, T., Diergaarde, P., Groenendijk, J., et al. (1997). The barley Mlo gene: a novel control element of plant pathogen resistance. Cell 88, 695-705 https://doi.org/10.1016/S0092-8674(00)81912-1
- Cheong, Y.H., Moon, B.C., Kim, J.K., Kim, C.Y., Kim, M.C., Kim, I.H., Park, C.Y., Kim, J.C., Park, B.O., Koo, S.C., et al. (2003). BWMK1, a rice mitogen-activated protein kinase, locates in the nucleus and mediates pathogenesis-related gene expression by activation of a transcription factor. Plant Physiol. 132, 1961-1972 https://doi.org/10.1104/pp.103.023176
- Chisholm, S.T., Coaker, G., Day, B., and Staskawicz, B.J. (2006). Host-microbe interactions: shaping the evolution of the plant immune response. Cell 124, 803-814 https://doi.org/10.1016/j.cell.2006.02.008
- Choi, M.S., Kim, M.C., Yoo, J.H., Moon, B.C., Koo, S.C., Park, B.O., Lee, J.H., Koo, Y.D., Han, H.J., Lee, S.Y., et al. (2005). Isolation of a calmodulin-binding transcription factor from rice (Oryza sativa L.). J. Biol. Chem. 280, 40820-40831 https://doi.org/10.1074/jbc.M504616200
- da Costa e Silva, O. (1994). CG-1, a parsley light-induced DNAbinding protein. Plant Mol. Biol. 25, 921-924 https://doi.org/10.1007/BF00028887
- Dangl, J.L., and Jones, J.D. (2001). Plant pathogens and integrated defence responses to infection. Nature 411, 826-833 https://doi.org/10.1038/35081161
- Dietrich, R.A., Richberg, M.H., Schmidt, R., Dean, C., and Dangl, J.L. (1997). A novel zinc finger protein is encoded by the Arabidopsis ipaN gene and functions as a negative regulator of plant cell death. Cell 88, 685-694 https://doi.org/10.1016/S0092-8674(00)81911-X
- Diez-Navajas, A.M., Greif, C., Poutaraud, A., and Merdinoglu, D. (2007). Two simplified fluorescent staining techniques to observe infection structures of the oomycete Plasmopara viticola in grapevine leaf tissues. Micron 38, 680-683 https://doi.org/10.1016/j.micron.2006.09.009
- Eulgem, T. (2005). Regulation of the Arabidopsis defense transcriptome. Trends Plant Sci. 10, 71-78 https://doi.org/10.1016/j.tplants.2004.12.006
- Finkler, A., Ashery-Padan, R., and Fromm, H. (2007). CAMTAs: calmodulin-binding transcription activators from plants to human. FEBS Lett. 581, 3893-3898 https://doi.org/10.1016/j.febslet.2007.07.051
- Galon, Y., Nave, R., Boyce, J.M., Nachmias, D., Knight, M.R., and Fromm, H. (2008). Calmodulin-binding transcription activator (CAMTA) 3 mediates biotic defense responses in Arabidopsis. FEBS Lett. 582, 943-948 https://doi.org/10.1016/j.febslet.2008.02.037
- Greenberg, J.T., and Yao, N. (2004). The role and regulation of programmed cell death in plant-pathogen interactions. Cell Microbiol. 6, 201-211 https://doi.org/10.1111/j.1462-5822.2004.00361.x
- Guimil, S., Chang, H.S., Zhu, T., Sesma, A., Osbourn, A., Roux, C., Ioannidis, V., Oakeley, E.J., Docquier, M., Descombes, P., et al. (2005). Comparative transcriptomics of rice reveals an ancient pattern of response to microbial colonization. Proc. Natl. Acad. Sci. USA 102, 8066-8070 https://doi.org/10.1073/pnas.0502999102
- Heil, M. (2002). Ecological costs of induced resistance. Curr. Opin. Plant Biol. 5, 345-350 https://doi.org/10.1016/S1369-5266(02)00267-4
- Heo, W.D., Lee, S.H., Kim, M.C., Kim, J.C., Chung, W.S., Chun, H.J., Lee, K.J., Park, C.Y., Park, H.C., Choi, J.Y., et al. (1999). Involvement of specific calmodulin isoforms in salicylic acidindependent activation of plant disease resistance responses. Proc. Natl. Acad. Sci. USA 96, 766-771 https://doi.org/10.1073/pnas.96.2.766
- Jeong, D.H., An, S., Kang, H.G., Moon, S., Han, J.J., Park, S., Lee, H.S., An, K., and An, G. (2002). T-DNA insertional mutagenesis for activation tagging in rice. Plant Physiol. 130, 1636-1644 https://doi.org/10.1104/pp.014357
- Jones, J.D., and Dangl, J.L. (2006). The plant immune system. Nature 444, 323-329 https://doi.org/10.1038/nature05286
- Jung, Y.H., Lee, J.H., Agrawal, G.K., Rakwal, R., Kim, J.A., Shim, J.K., Lee, S.K., Jeon, J.S., Koh, H.J., Lee, Y.H., et al. (2005). The rice (Oryza sativa) blast lesion mimic mutant, blm, may confer resistance to blast pathogens by triggering multiple defense-associated signaling pathways. Plant Physiol. Biochem. 43, 397-406 https://doi.org/10.1016/j.plaphy.2005.03.002
- Kim, M.C., Panstruga, R., Elliott, C., Muller, J., Devoto, A., Yoon, H.W., Park, H.C., Cho, M.J., and Schulze-Lefert, P. (2002a). Calmodulin interacts with MLO protein to regulate defence against mildew in barley. Nature 416, 447-451 https://doi.org/10.1038/416447a
- Kim, M.C., Lee, S.H., Kim, J.K., Chun, H.J., Choi, M.S., Chung, W.S., Moon, B.C., Kang, C.H., Park, C.Y., Yoo, J.H., et al. (2002b). Mlo, a modulator of plant defense and cell death, is a novel calmodulin-binding protein. Isolation and characterization of a rice Mlo homologue. J. Biol. Chem. 277, 19304-19314 https://doi.org/10.1074/jbc.M108478200
- Kim, C.Y., Koo, Y.D., Jin, J.B., Moon, B.C., Kang, C.H., Kim, S.T., Park, B.O., Lee, S.Y., Kim, M.L., Hwang, I., et al. (2003). Rice C2-domain proteins are induced and translocated to the plasma membrane in response to a fungal elicitor. Biochemistry 42, 11625-11633 https://doi.org/10.1021/bi034576n
- Kim, S.T., Kim, S.G., Hwang, D.H., Kang, S.Y., Kim, H.J., Lee, B.H., Lee, J.J., and Kang, K.Y. (2004). Proteomic analysis of pathogen-responsive proteins from rice leaves induced by rice blast fungus, Magnaporthe grisea. Proteomics 4, 3569-3578 https://doi.org/10.1002/pmic.200400999
- Kottapalli, K.R., Rakwal, R., Satoh, K., Shibato, J., Kottapalli, P., Iwahashi, H., and Kikuchi, S. (2007). Transcriptional profiling of indica rice cultivar IET8585 (Ajaya) infected with bacterial leaf blight pathogen Xanthomonas oryzae pv oryzae. Plant Physiol. Biochem. 45, 834-850 https://doi.org/10.1016/j.plaphy.2007.07.013
- Lee, S., Kim, J., Son, J.S., Nam, J., Jeong, D.H., Lee, K., Jang, S., Yoo, J., Lee, J., Lee, D.Y., et al. (2003). Systematic reverse genetic screening of T-DNA tagged genes in rice for functional genomic analyses: MADS-box genes as a test case. Plant Cell Physiol. 44, 1403-1411 https://doi.org/10.1093/pcp/pcg156
- Lorrain, S., Vailleau, F., Balague, C., and Roby, D. (2003). Lesion mimic mutants: keys for deciphering cell death and defense pathways in plants? Trends Plant Sci. 8, 263-271 https://doi.org/10.1016/S1360-1385(03)00108-0
- Ma, W., and Berkowitz, G.A. (2007). The grateful dead: calcium and cell death in plant innate immunity. Cell Microbiol. 9, 2571-2585 https://doi.org/10.1111/j.1462-5822.2007.01031.x
- Maleck, K., Levine, A., Eulgem, T., Morgan, A., Schmid, J., Lawton, K.A., Dangl, J.L., and Dietrich, R.A. (2000). The transcriptome of Arabidopsis thaliana during systemic acquired resistance. Nat. Genet. 26, 403-410 https://doi.org/10.1038/82521
- McGee, J.D., Hamer, J.E., and Hodges, T.K. (2001). Characterization of a PR-10 pathogenesis-related gene family induced in rice during infection with Magnaporthe grisea. Mol. Plant Microbe. Interact. 14, 877-886 https://doi.org/10.1094/MPMI.2001.14.7.877
- Park, C.Y., Lee, J.H., Yoo, J.H., Moon, B.C., Choi, M.S., Kang, Y.H., Lee, S.M., Kim, H.S., Kang, K.Y., Chung, W.S., et al. (2005). WRKY group IId transcription factors interact with calmodulin. FEBS Lett. 579, 1545-1550 https://doi.org/10.1016/j.febslet.2005.01.057
- Reddy, A.S., Reddy, V.S., and Golovkin, M. (2000). A calmodulin binding protein from Arabidopsis is induced by ethylene and contains a DNA-binding motif. Biochem. Biophys. Res. Commun. 279, 762-769 https://doi.org/10.1006/bbrc.2000.4032
- Snedden, W.A., and Fromm, H. (1998) Calmodulin, calmodulinrelated proteins and plant responses to the environment. Trends Plant Sci. 5, 154-159 https://doi.org/10.1016/S1360-1385(98)01284-9
- Szymanski, D.B., Liao, B., and Zielinski, R.E. (1996). Calmodulin isoforms differentially enhance the binding of cauliflower nuclear proteins and recombinant TGA3 to a region derived from the Arabidopsis Cam-3 promoter. Plant Cell 8, 1069-1077 https://doi.org/10.1105/tpc.8.6.1069
- Takabatake, R., Karita, E., Seo, S., Mitsuhara, I., Kuchitsu, K., and Ohashi, Y. (2007). Pathogen-induced calmodulin isoforms in basal resistance against bacterial and fungal pathogens in tobacco. Plant Cell Physiol. 48, 414-423 https://doi.org/10.1093/pcp/pcm011
- Tao, Y., Xie, Z., Chen, W., Glazebrook, J., Chang, H.S., Han, B., Zhu, T., Zou, G., and Katagiri, F. (2003). Quantitative nature of Arabidopsis responses during compatible and incompatible interactions with the bacterial pathogen Pseudomonas syringae. Plant Cell 15, 317-330 https://doi.org/10.1105/tpc.007591
- Veronese, P., Ruiz, M.T., Coca, M.A., Hernandez-Lopez, A., Lee, H., Ibeas, J.I., Damsz, B., Pardo, J.M., Hasegawa, P.M., Bressan, R.A., et al. (2003). In defense against pathogens. Both plant sentinels and foot soldiers need to know the enemy. Plant Physiol. 131, 1580-1590 https://doi.org/10.1104/pp.102.013417
- White, P.J., and Broadley, M.R. (2003). Calcium in plants. Ann. Bot. (Lond). 92, 487-511 https://doi.org/10.1093/aob/mcg164
- Yang, T., and Poovaiah, B.W. (2000). An early ethylene upregulated gene encoding a calmodulin-binding protein involved in plant senescence and death. J. Biol. Chem. 275, 38467-38473 https://doi.org/10.1074/jbc.M003566200
- Yang, T., and Poovaiah, B.W. (2002). A calmodulin-binding/CGCG box DNA-binding protein family involved in multiple signaling pathways in plants. J. Biol. Chem. 277, 45049-45058 https://doi.org/10.1074/jbc.M207941200
- Yang, T., and Poovaiah, B.W. (2003). Calcium/calmodulin-mediated signal network in plants. Trends Plant Sci. 8, 505-512 https://doi.org/10.1016/j.tplants.2003.09.004
- Yin, Z., Chen, J., Zeng, L., Goh, M., Leung, H., Khush, G.S., and Wang, G.L. (2000). Characterizing rice lesion mimic mutants and identifying a mutant with broad-spectrum resistance to rice blast and bacterial blight. Mol. Plant Microbe. Interact. 13, 869-876 https://doi.org/10.1094/MPMI.2000.13.8.869
- Yoo, J.H., Park, C.Y., Kim, J.C., Heo, W.D., Cheong, M.S., Park, H.C., Kim, M.C., Moon, B.C., Choi, M.S., Kang, Y.H., et al. (2005). Direct interaction of a divergent CaM isoform and the transcription factor, MYB2, enhances salt tolerance in Arabidopsis. J. Biol. Chem. 280, 3697-3706 https://doi.org/10.1074/jbc.M408237200
- Yu, I.C., Parker, J., and Bent, A.F. (1998). Gene-for-gene disease resistance without the hypersensitive response in Arabidopsis dnd1 mutant. Proc. Natl. Acad. Sci. USA 95, 7819-7824 https://doi.org/10.1073/pnas.95.13.7819
- Zegzouti, H., Jones, B., Frasse, P., Marty, C., Maitre, B., Latch, A., Pech, J.C., and Bouzayen, M. (1999). Ethylene-regulated gene expression in tomato fruit: characterization of novel ethyleneresponsive and ripening-related genes isolated by differential display. Plant J. 18, 589-600 https://doi.org/10.1046/j.1365-313x.1999.00483.x
Cited by
- Breaking the code: Ca2+ sensors in plant signalling vol.425, pp.1, 2009, https://doi.org/10.1042/bj20091147
- T-DNA 돌연변이를 이용한 벼 기능 유전체 연구 vol.37, pp.2, 2010, https://doi.org/10.5010/jpb.2010.37.2.133
- Characterization of novel calmodulin binding domains within IQ motifs of IQGAP1 vol.32, pp.6, 2009, https://doi.org/10.1007/s10059-011-0109-4
- Sequence analysis and expression of the calmodulin gene, MCaM-3, in mulberry (Morus L.) vol.33, pp.2, 2009, https://doi.org/10.1007/s13258-010-0124-4
- Suppression of DS1 Phosphatidic Acid Phosphatase Confirms Resistance to Ralstonia solanacearum in Nicotiana benthamiana vol.8, pp.9, 2009, https://doi.org/10.1371/journal.pone.0075124
- Structural Analysis of a Calmodulin Variant from Rice : THE C-TERMINAL EXTENSION OF OsCaM61 REGULATES ITS CALCIUM BINDING AND ENZYME ACTIVATION PROPERTIES vol.288, pp.44, 2009, https://doi.org/10.1074/jbc.m113.491076
- Tomato SR/CAMTA transcription factors SlSR1 and SlSR3L negatively regulate disease resistance response and SlSR1L positively modulates drought stress tolerance vol.14, pp.None, 2009, https://doi.org/10.1186/s12870-014-0286-3
- Regulatory interplay between soybean root and soybean cyst nematode during a resistant and susceptible reaction vol.14, pp.None, 2014, https://doi.org/10.1186/s12870-014-0300-9
- Calmodulin-binding transcription activators and perspectives for applications in biotechnology vol.99, pp.24, 2009, https://doi.org/10.1007/s00253-015-6966-6
- Genome-wide identification of CAMTA gene family members in Medicago truncatula and their expression during root nodule symbiosis and hormone treatments vol.6, pp.None, 2009, https://doi.org/10.3389/fpls.2015.00459
- Identification and expression profiling analysis of calmodulin-binding transcription activator genes in maize ( Zea mays L.) under abiotic and biotic stresses vol.6, pp.None, 2009, https://doi.org/10.3389/fpls.2015.00576
- Phylogeny of Plant CAMTAs and Role of AtCAMTAs in Nonhost Resistance to Xanthomonas oryzae pv. oryzae vol.7, pp.None, 2009, https://doi.org/10.3389/fpls.2016.00177
- Brassica napus Genome Possesses Extraordinary High Number of CAMTA Genes and CAMTA3 Contributes to PAMP Triggered Immunity and Resistance to Sclerotinia sclerotiorum vol.7, pp.None, 2009, https://doi.org/10.3389/fpls.2016.00581
- Genome-Wide Identification of Dicer-Like, Argonaute, and RNA-Dependent RNA Polymerase Gene Families in Brassica Species and Functional Analyses of Their Arabidopsis Homologs in Resistance to Sclero vol.7, pp.None, 2009, https://doi.org/10.3389/fpls.2016.01614
- Global gene expression analysis using RNA-seq uncovered a new role for SR1/CAMTA3 transcription factor in salt stress vol.6, pp.None, 2016, https://doi.org/10.1038/srep27021
- Cloning and Stress-Induced Expression Analysis of Calmodulin in the Antarctic Alga Chlamydomonas sp. ICE-L vol.74, pp.8, 2009, https://doi.org/10.1007/s00284-017-1263-5
- Positive interactions of major-effect QTLs with genetic background that enhances rice yield under drought vol.8, pp.None, 2009, https://doi.org/10.1038/s41598-018-20116-7
- Genetic Dissection of Grain Nutritional Traits and Leaf Blight Resistance in Rice vol.10, pp.1, 2019, https://doi.org/10.3390/genes10010030
- Phaseolus vulgaris genome possesses CAMTA genes, and phavuCAMTA1 contributes to the drought tolerance vol.98, pp.1, 2019, https://doi.org/10.1007/s12041-019-1069-2
- Ca 2+ /Calmodulin Complex Triggers CAMTA Transcriptional Machinery Under Stress in Plants: Signaling Cascade and Molecular Regulation vol.11, pp.None, 2009, https://doi.org/10.3389/fpls.2020.598327
- Rice CaM-binding transcription factor (OsCBT) mediates defense signaling via transcriptional reprogramming vol.14, pp.3, 2009, https://doi.org/10.1007/s11816-020-00603-y