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Arabidopsis lysin-motif proteins LYM1 LYM3 CERK1 mediate bacterial peptidoglycan sensing and immunity to bacterial infection
Arabidopsis lysin-motif proteins LYM1 LYM3 CERK1 mediate bacterial peptidoglycan sensing and immunity to bacterial infection
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Arabidopsis lysin-motif proteins LYM1 LYM3 CERK1 mediate bacterial peptidoglycan sensing and immunity to bacterial infection
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Arabidopsis lysin-motif proteins LYM1 LYM3 CERK1 mediate bacterial peptidoglycan sensing and immunity to bacterial infection
Arabidopsis lysin-motif proteins LYM1 LYM3 CERK1 mediate bacterial peptidoglycan sensing and immunity to bacterial infection

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Arabidopsis lysin-motif proteins LYM1 LYM3 CERK1 mediate bacterial peptidoglycan sensing and immunity to bacterial infection
Arabidopsis lysin-motif proteins LYM1 LYM3 CERK1 mediate bacterial peptidoglycan sensing and immunity to bacterial infection
Journal Article

Arabidopsis lysin-motif proteins LYM1 LYM3 CERK1 mediate bacterial peptidoglycan sensing and immunity to bacterial infection

2011
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Overview
Recognition of microbial patterns by host pattern recognition receptors is a key step in immune activation in multicellular eukaryotes. Peptidoglycans (PGNs) are major components of bacterial cell walls that possess immunity-stimulating activities in metazoans and plants. Here we show that PGN sensing and immunity to bacterial infection in Arabidopsis thaliana requires three lysin-motif (LysM) domain proteins. LYM1 and LYM3 are plasma membrane proteins that physically interact with PGNs and mediate Arabidopsis sensitivity to structurally different PGNs from Gram-negative and Gram-positive bacteria. lym1 and lym3 mutants lack PGN-induced changes in transcriptome activity patterns, but respond to fungus-derived chitin, a pattern structurally related to PGNs, in a wild-type manner. Notably, lym1, lym3, and lym3 lym1 mutant genotypes exhibit supersusceptibility to infection with virulent Pseudomonas syringae pathovar tomato DC3000. Defects in basal immunity in lym3 lym1 double mutants resemble those observed in lym1 and lym3 single mutants, suggesting that both proteins are part of the same recognition system. We further show that deletion of CERK1, a LysM receptor kinase that had previously been implicated in chitin perception and immunity to fungal infection in Arabidopsis, phenocopies defects observed in lym1 and lym3 mutants, such as peptidoglycan insensitivity and enhanced susceptibility to bacterial infection. Altogether, our findings suggest that plants share with metazoans the ability to recognize bacterial PGNs. However, as Arabidopsis LysM domain proteins LYM1, LYM3, and CERK1 form a PGN recognition system that is unrelated to metazoan PGN receptors, we propose that lineage-specific PGN perception systems have arisen through convergent evolution.
Publisher
National Academy of Sciences,National Acad Sciences
Subject

Animalia

/ Arabidopsis

/ Arabidopsis - genetics

/ Arabidopsis - metabolism

/ Arabidopsis - microbiology

/ Arabidopsis Proteins - classification

/ Arabidopsis Proteins - genetics

/ Arabidopsis Proteins - metabolism

/ Arabidopsis thaliana

/ Bacteria

/ Bacteria - growth & development

/ Bacteria - immunology

/ Bacteria - metabolism

/ Bacterial diseases

/ Bacterial infections

/ Biological Sciences

/ Cell membranes

/ cell walls

/ Chitin

/ convergent evolution

/ Disease Resistance - genetics

/ Disease Resistance - immunology

/ Eukaryotes

/ eukaryotic cells

/ Flowers & plants

/ fungi

/ Gene expression

/ Gene Expression Regulation, Plant

/ Genotype & phenotype

/ Genotypes

/ Gram-positive bacteria

/ Green Fluorescent Proteins - genetics

/ Green Fluorescent Proteins - metabolism

/ Host-Pathogen Interactions - immunology

/ Immunity

/ Immunoblotting

/ Innate immunity

/ Life Sciences

/ Ligands

/ Lycopersicon esculentum

/ membrane proteins

/ Metazoa

/ Microscopy, Confocal

/ Mutants

/ Mutation

/ Oligonucleotide Array Sequence Analysis

/ pathovars

/ Pattern recognition

/ Peptidoglycan - immunology

/ Peptidoglycan - metabolism

/ peptidoglycans

/ Phylogeny

/ Plant cells

/ Plant Diseases - genetics

/ Plant Diseases - immunology

/ Plant Diseases - microbiology

/ Plants

/ Plants, Genetically Modified

/ plasma membrane

/ Protein-Serine-Threonine Kinases - genetics

/ Protein-Serine-Threonine Kinases - metabolism

/ Proteins

/ Pseudomonas syringae

/ Pseudomonas syringae - immunology

/ Pseudomonas syringae - metabolism

/ Pseudomonas syringae - physiology

/ Receptors

/ Reverse Transcriptase Polymerase Chain Reaction

/ Staphylococcus aureus - immunology

/ Staphylococcus aureus - metabolism

/ Staphylococcus aureus - physiology

/ Tomatoes

/ Transcriptome

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