Оптимизация автоматических систем регулирования. Часть 3. by Новиков С.И.

By Новиков С.И.

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F. (1996). Identification and map location of TTR1, a single locus in Arabidopsis thaliana that confers tolerance to tobacco ringspot nepovirus. Mol. Plant-Microbe Interact. 9:729–735. Lee, S. , Han, S. , Bartley, L. , and Ronald, P. C. (2006). From the Academy: Colloquium review. Unique characteristics of Xanthomonas oryzae pv. oryzae AvrXa21 and implications for plant innate immunity. Proc. Natl. Acad. Sci. U. S. A. 103:18395–18400. Leister, R. , and Staskawicz, B. J. (2005). Molecular genetic evidence for the role of SGT1 in the intramolecular complementation of Bs2 protein activity in Nicotiana benthamiana.

Tobacco mosaic virus assembly and disassembly: Determinants in pathogenicity and resistance. Annu. Rev. Phytopathol. 40:287–308. Dangl, J. , and Jones, J. D. (2001). Plant pathogens and integrated defence responses to infection. Nature 411:826–833. Dardick, C. , and Culver, J. N. (1999). Comparison of tobamovirus coat protein structural features that affect elicitor activity in pepper, eggplant, and tobacco. Mol. Plant-Microbe Interact. 12:247–251. Diaz-Pendon, J. -W. (2008). Direct and indirect roles of viral suppressors of RNA silencing in pathogenesis.

2008). Another possibility for antiviral defense occurs at the transcriptional level, and is encountered with DNA viruses. , 2006). 2. Amplification of silencing response The third family of proteins involved in silencing in plants is the RDR family. In plants there are six RDR paralogs: RDR1, RDR2, RDR3a (RDR3), RDR3b (RDR4), RDR3c (RDR5) and RDR6 (SDE1/SGS-2). The putative catalytic domain is the DLDGD motif, which is highly conserved among all RDRs identified (Wassenegger and Krczal, 2006).

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