The malectin-like receptor-like kinase LETUM1 modulates NLR protein SUMM2 activation via MEKK2 scaffolding
The innate immune system detects pathogen-derived molecules via specialized immune receptors to prevent infections 1 – 3 . Plant immune receptors include cell surface-resident pattern recognition receptors (PRRs, including receptor-like kinases (RLKs)), and intracellular nucleotide-binding domain le...
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Published in | Nature plants Vol. 6; no. 9; pp. 1106 - 1115 |
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Main Authors | , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
01.09.2020
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
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Summary: | The innate immune system detects pathogen-derived molecules via specialized immune receptors to prevent infections
1
–
3
. Plant immune receptors include cell surface-resident pattern recognition receptors (PRRs, including receptor-like kinases (RLKs)), and intracellular nucleotide-binding domain leucine-rich repeat proteins (NLRs). It remains enigmatic how RLK- and NLR-mediated signalling are connected. Disruption of an immune-activated MEKK1–MKK1/2–MPK4 MAPK cascade activates the NLR SUMM2 via the MAPK kinase kinase MEKK2, leading to autoimmunity
4
–
9
. To gain insights into the mechanisms underlying SUMM2 activation, we used an RNA interference-based genetic screen for
mekk1
autoimmune suppressors and identified an uncharacterized malectin-like RLK, named LETUM1 (LET1), as a specific regulator of
mekk1–mkk1/2
–
mpk4
autoimmunity via complexing with both SUMM2 and MEKK2. MEKK2 scaffolds LET1 and SUMM2 for protein stability and association, and counter-regulates the F-box protein CPR1-mediated SUMM2 ubiquitination and degradation, thereby regulating SUMM2 accumulation and activation. Our study indicates that malectin-like RLK LET1 senses the perturbance of cellular homoeostasis caused by the deficiency in immune-activated signalling and activates the NLR SUMM2-mediated autoimmunity via MEKK2 scaffolding.
Plants with loss of function mutations in the MEKK1–MKK1/2–MPK4 MAP kinase pathway show strong autoimmunity phenotypes and dwarfism. Through a suppressor genetic screen, the malectin-like receptor kinase LET1 is identified as a new regulator of immune signalling. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Y.H., J.L., L.S., and P.H. conceived the project, designed experiments and analyzed data. J.L., Y.H., L.K., X.Y., B.F., D.L., B.Z., G.C.M., P.Y., and D.G. performed experiments and analyzed data. W.M.W, E.P.B.F., and P.L. analyzed data and provided critical feedback. L.S., and P.H. wrote the manuscript with inputs from all co-authors. Author Contributions |
ISSN: | 2055-0278 2055-0278 |
DOI: | 10.1038/s41477-020-0748-6 |