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Reactive oxygen species (ROS) and defence response in plants Group leader: Miguel Angel Torres Study of function of the Reactive Oxygen Species (ROS) produced by the NADPH oxidase in response to pathogens and other responses to the environment in Arabidopsis. The goal is to decipher, using functional genomics tools, the functions of the plant NADPH oxidase gene family. Different members of the rboh (respiratory burst oxidase homologues) family, components of the plant NADPH oxidase, control production of ROS during defense and other responses. We are performing this research in Arabidopsis, model organism for studies in plants, where many genomic tools are available. We intend to further the identification of the factors that regulate Atrboh function, as well as putative Production of ROS and cell death in response to different pathogens. targets or mediators of Detection of H2O2 by diaminobenzidine stain (top) and cell death monitored by trypan blue stain (bottom) in Arabidopsis leaves infected ROS-dependent signaling. with different pathogens. Relevant results My research work during 2004-2006 has been carried out at the University of North Carolina, at Jeff Dangl’s laboratory,. There, we pioneered studies in the field of production of reactive oxygen species in plants, particularly in the plant-pathogen interactions, and we made important contribution to dissect the NADPH oxidase function in plants, that I intend to continue now with my own group. Our previous work provided genetic evidence that the plant NADPH oxidase is responsible for the apoplastic ROS produced following pathogen recognition (Torres et al., 2002). This finding solved a mystery set into motion by Doke’s work nearly 20 years ago. Additional studies confirmed and generalized our findings (see Torres and Dangl, 2005). We also attributed clear developmental and cell biological functions to several members of the Atrboh gene family. We have collaborated with experts studying those processes to further dissect the function of ROS in stomata closure and root hair development. (Kwak et al., 2003). (Foreman et al., 2003). Interestingly, both works indicate that NADPH oxidase-derived ROS can control processes by regulating the activation of Ca2+ channels. During this latest period, we furthered these studies and demonstrated that pathogen-induced, NADPH oxidase-derived ROS regulate differentially pathogen induced cell death depending on the interaction. Whereas Rbohderived ROS are positive regulators of the HR induced by an avirulent bacteria, they are negative regulators of the cell death after an The Arabidopsis NAPDH oxidase AtrbohD is avirulent oomycete (Torres et al., 2002). In responsible for the production of most ROS addition Rboh-derived ROS are negative in response to pathogens. DAB stain of 4 regulators of the unrestricted cell death that weeks old leaves from different genotypes. surrounds the initial HR in the lesion mimic mutant lsd1 (Torres et al., 2005). These data demonstrated that ROS derived from Atrboh-containing NADPH oxidases are not cellular killers, but rather function as signaling molecules to protect cells from cell death. Interestingly, whereas NADPH oxidase-derived ROS and SA were proposed to act synergistically driving the HR, both signals antagonize in the regulation of cell death expansion at the margins of the HR lesions in lsd1. This underscores how ROS can mediate different functions in different cellular compartments and spatial context, and in relation to other regulatory signals. Recent Publications Torres, M. A., et al. (2006) Plant Physiol 141, 373-378 Torres, M. A., et al. (2005) Nat Genet 37, 1130-1134 Torres, M. A., and Dangl, J. L. (2005) Curr Opin Plant Biol 8, 397-.