A nuclear localization for Avr2 from Fusarium oxysporum is required to activate the tomato resistance protein I-2

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Abstract

Plant pathogens secrete effector proteins to promote host colonization. During infection of tomato xylem vessels, Fusarium oxysporum f. sp. lycopersici (Fol) secretes the Avr2 effector protein. Besides being a virulence factor, Avr2 is recognized intracellularly by the tomato I-2 resistance protein, resulting in the induction of host defenses. Here, we show that AVR2 is highly expressed in root- and xylem-colonizing hyphae three days post inoculation of roots. Co-expression of I-2 with AVR2 deletion constructs using agroinfiltration in Nicotiana benthamiana leaves revealed that, except for the N-terminal 17 amino acids, the entire AVR2 protein is required to trigger I-2-mediated cell death. The truncated Avr2 variants are still able to form homo-dimers, showing that the central region of Avr2 is required for dimerization. Simultaneous production of I-2 and Avr2 chimeras carrying various subcellular localization signals in N. benthamiana leaves revealed that a nuclear localization of Avr2 is required to trigger I-2-dependent cell death. Nuclear exclusion of Avr2 prevented its activation of I-2, suggesting that Avr2 is recognized by I-2 in the nucleus. © 2013 Ma, Cornelissen and Takken.

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Ma, L., Cornelissen, B. J. C., & Takken, F. L. W. (2013). A nuclear localization for Avr2 from Fusarium oxysporum is required to activate the tomato resistance protein I-2. Frontiers in Plant Science, 4(APR). https://doi.org/10.3389/fpls.2013.00094

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