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The tomato subtilase family includes several cell death-related proteinases with caspase specificity

GND
1130189864
Zugehörigkeit
Institute of Plant Physiology and Biotechnology, University of Hohenheim, 70593, Stuttgart, Germany
Reichardt, Sven;
GND
1163746045
Zugehörigkeit
Institute of Plant Physiology and Biotechnology, University of Hohenheim, 70593, Stuttgart, Germany
Repper, Dagmar;
Zugehörigkeit
Belozersky Institute of Physico-Chemical Biology, Moscow State University, Moscow, 119991, Russia
Tuzhikov, Alexander I.;
Zugehörigkeit
Belozersky Institute of Physico-Chemical Biology, Moscow State University, Moscow, 119991, Russia
Galiullina, Raisa A.;
Zugehörigkeit
Centre for Research in Agricultural Genomics, CSIC-IRTA-UAB-UB, Campus UAB, Bellaterra, Barcelona, 08193, Spain
Planas-Marques, Marc;
Zugehörigkeit
Belozersky Institute of Physico-Chemical Biology, Moscow State University, Moscow, 119991, Russia
Chichkova, Nina V.;
Zugehörigkeit
Belozersky Institute of Physico-Chemical Biology, Moscow State University, Moscow, 119991, Russia
Vartapetian, Andrey B.;
GND
1099923298
Zugehörigkeit
Institute of Plant Physiology and Biotechnology, University of Hohenheim, 70593, Stuttgart, Germany
Stintzi, Annick;
GND
1017623899
Zugehörigkeit
Institute of Plant Physiology and Biotechnology, University of Hohenheim, 70593, Stuttgart, Germany
Schaller, Andreas

Phytaspases are Asp-specific subtilisin-like plant proteases that have been likened to animal caspases with respect to their regulatory function in programmed cell death (PCD). We identified twelve putative phytaspase genes in tomato that differed widely in expression level and tissue-specific expression patterns. Most phytaspase genes are tandemly arranged on tomato chromosomes one, four, and eight, and many belong to taxon-specific clades, e.g. the P69 clade in the nightshade family, suggesting that these genes evolved by gene duplication after speciation. Five tomato phytaspases (SlPhyts) were expressed in N. benthamiana and purified to homogeneity. Substrate specificity was analyzed in a proteomics assay and with a panel of fluorogenic peptide substrates. Similar to animal caspases, SlPhyts recognized an extended sequence motif including Asp at the cleavage site. Clear differences in cleavage site preference were observed implying different substrates in vivo and, consequently, different physiological functions. A caspase-like function in PCD was confirmed for five of the seven tested phytaspases. Cell death was triggered by ectopic expression of SlPhyts 2, 3, 4, 5, 6 in tomato leaves by agro-infiltration, as well as in stably transformed transgenic tomato plants. SlPhyts 3, 4, and 5 were found to contribute to cell death under oxidative stress conditions.

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