Journal Article

Indirect activation of a plant nucleotide binding site-leucine-rich repeat protein by a bacterial protease

Golstein, Catherine, Innes, Roger W, Ade, Jules, DeYoung, Brody J

2007

Overview

Nucleotide binding site-leucine-rich repeat (NBS-LRR) proteins mediate pathogen recognition in both mammals and plants. The molecular mechanisms by which pathogen molecules activate NBS-LRR proteins are poorly understood. Here we show that RPS5, a NBS-LRR protein from Arabidopsis, is activated by AvrPphB, a bacterial protease, via an indirect mechanism. When transiently expressed in Nicotiana benthamiana leaves, full-length RPS5 protein triggered programmed cell death, but only when coexpressed with AvrPphB and a second Arabidopsis protein, PBS1, which is a specific substrate of AvrPphB. Using coimmunoprecipitation analysis, we found that PBS1 is in a complex with the N-terminal coiled coil (CC) domain of RPS5 before exposure to AvrPphB. Deletion of the RPS5 LRR domain caused RPS5 to constitutively activate programmed cell death, even in the absence of AvrPphB and PBS1, and this activation depended on both the CC and NBS domains. The LRR and CC domains both coimmunoprecipitate with the NBS domain but not with each other. Thus, the LRR domain appears to function in part to inhibit RPS5 signaling, and cleavage of PBS1 by AvrPphB appears to release RPS5 from this inhibition. An amino acid substitution in the NBS site of RPS5 that is known to inhibit ATP binding in other NBS-LRR proteins blocked activation of RPS5, whereas a substitution thought to inhibit ATP hydrolysis constitutively activated RPS5. Combined, these data suggest that ATP versus ADP binding functions as a molecular switch that is flipped by cleavage of PBS1.

• Publisher: National Academy of Sciences,National Acad Sciences
• Subject: Adenosine diphosphate / Adenosine Diphosphate - metabolism / adenosine triphosphate / Adenosine Triphosphate - metabolism / Amino acids / Apoptosis / Arabidopsis / Arabidopsis Proteins - genetics / Arabidopsis Proteins - metabolism / Arabidopsis thaliana / ATP / Bacteria / bacterial diseases of plants / Bacterial Proteins - genetics / Bacterial Proteins - metabolism / binding capacity / Binding Sites / Biological Sciences / Cell death / Cells / disease resistance / Flowers & plants / Gels / host-pathogen relationships / Leucine-Rich Repeat Proteins / Mathematical functions / Molecules / Nicotiana - genetics / Nicotiana benthamiana / nucleotide binding site-leucine-rich repeat proteins / Nucleotides / Pathogens / Peptide Hydrolases - metabolism / Plant cells / plant proteins / Plasmids / Proteases / Protein Serine-Threonine Kinases - metabolism / protein-protein interactions / proteinases / Proteins / Proteins - metabolism / proteolysis / Pseudomonas syringae / Transfection