Back to Search
Start Over
The ZAR1 resistosome is a calcium-permeable channel triggering plant immune signaling
- Source :
- Cell. 184(13)
- Publication Year :
- 2021
-
Abstract
- Nucleotide-binding, leucine-rich repeat receptors (NLRs) are major immune receptors in plants and animals. Upon activation, the Arabidopsis NLR protein ZAR1 forms a pentameric resistosome in vitro and triggers immune responses and cell death in plants. In this study, we employed single-molecule imaging to show that the activated ZAR1 protein can form pentameric complexes in the plasma membrane. The ZAR1 resistosome displayed ion channel activity in Xenopus oocytes in a manner dependent on a conserved acidic residue Glu11 situated in the channel pore. Pre-assembled ZAR1 resistosome was readily incorporated into planar lipid-bilayers and displayed calcium-permeable cation-selective channel activity. Furthermore, we show that activation of ZAR1 in the plant cell led to Glu11-dependent Ca2+ influx, perturbation of subcellular structures, production of reactive oxygen species, and cell death. The results thus support that the ZAR1 resistosome acts as a calcium-permeable cation channel to trigger immunity and cell death.
- Subjects :
- Programmed cell death
Cell Membrane Permeability
Xenopus
Lipid Bilayers
Arabidopsis
chemistry.chemical_element
Glutamic Acid
Calcium
General Biochemistry, Genetics and Molecular Biology
03 medical and health sciences
0302 clinical medicine
Immune system
Plant Cells
Animals
Plant Immunity
Receptor
030304 developmental biology
Disease Resistance
chemistry.chemical_classification
0303 health sciences
Reactive oxygen species
biology
Cell Death
Arabidopsis Proteins
Calcium channel
Protoplasts
Cell Membrane
biology.organism_classification
Single Molecule Imaging
Cell biology
chemistry
Vacuoles
Oocytes
Protein Multimerization
Carrier Proteins
Reactive Oxygen Species
030217 neurology & neurosurgery
Signal Transduction
Subjects
Details
- ISSN :
- 10974172
- Volume :
- 184
- Issue :
- 13
- Database :
- OpenAIRE
- Journal :
- Cell
- Accession number :
- edsair.doi.dedup.....17f684726021968b11d130c88f9964b1