2022
DOI: 10.1038/s41477-022-01167-1
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Deconvoluting signals downstream of growth and immune receptor kinases by phosphocodes of the BSU1 family phosphatases

Abstract: Hundreds of leucine-rich repeat receptor kinases (LRR-RKs) have evolved to control diverse processes of growth, development, and immunity in plants; the mechanisms that link LRR-RKs to distinct cellular responses are not understood. Here we show that two LRR-RKs, the brassinosteroid hormone receptor BRI1 (BRASSINOSTEROID INSENSITIVE 1) and the flagellin receptor FLS2 (FLAGELLIN SENSING 2), regulate downstream glycogen synthase kinase 3 (GSK3) and mitogen-activated protein (MAP) kinases, respectively, through p… Show more

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Cited by 14 publications
(8 citation statements)
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“…Recent study reveals that loss of BSU1 family phosphatases activates effector-triggered immunity (ETI) and impairs flagellin-triggered MAP kinase activation and immunity, the mechanism of which is that BIK1 enhances the flagellin-induced MAP kinase activation and immunity through phosphorylating BSU1 at serine-251 (S251), whereas it does not affect immune signaling by phosphorylating at S764, an important phosphorylation site mediating the interaction between BSU1 and BIN2, of which BIN2 is induced by CDG1 in BRs-BRI1 signaling. These results indicate that BSU1 plays an essential role in immunity and transduces BR-BRI1 and flagellin-FLS2 signals by different phosphorylation sites …”
Section: Crosstalk Between Brs Signal and Immune Signalsmentioning
confidence: 81%
See 1 more Smart Citation
“…Recent study reveals that loss of BSU1 family phosphatases activates effector-triggered immunity (ETI) and impairs flagellin-triggered MAP kinase activation and immunity, the mechanism of which is that BIK1 enhances the flagellin-induced MAP kinase activation and immunity through phosphorylating BSU1 at serine-251 (S251), whereas it does not affect immune signaling by phosphorylating at S764, an important phosphorylation site mediating the interaction between BSU1 and BIN2, of which BIN2 is induced by CDG1 in BRs-BRI1 signaling. These results indicate that BSU1 plays an essential role in immunity and transduces BR-BRI1 and flagellin-FLS2 signals by different phosphorylation sites …”
Section: Crosstalk Between Brs Signal and Immune Signalsmentioning
confidence: 81%
“…These results indicate that BSU1 plays an essential role in immunity and transduces BR-BRI1 and flagellin-FLS2 signals by different phosphorylation sites. 99 43 At the signal transduction level, the crosstalk between the BR signal and the PTI signal is mainly based on BIK1/BSK1/BSU1/BIN2. BIK1 mediates inverse functions in the PTI and BR signals via dynamic association with specific receptor complexes and differential phosphorylation events.…”
Section: Functions Of Brs In Pathogen Resistancementioning
confidence: 99%
“…For a concise prediction comparison, we compiled a short list of functionally important phosphosites, validated in A. thaliana , involved in the brassinosteroid (BR), ethylene (ET), and abscisic acid (ABA) pathways. In the BR pathway, we included BRASSINOSTEROID INSENSITIVE 1 (BRI1) Y831 and Y956 (Bojar et al, 2014 ; Oh et al, 2009 ), BRASSINOSTEROID‐INSENSITIVE2 (BIN2) S187, S203, and Y200 (Kim et al, 2009 ; Xiong et al, 2017 ), BRASSINAZOLE RESISTANT1 (BZR1) Thr173 and Thr177 (Ryu et al, 2007 ), and BRI1‐SUPPRESSOR1 (BSU1) Ser251 and Ser764 (Park et al, 2022 ). In the ET pathway, we included ETHYLENE INSENSITIVE3 (EIN3) Thr174 and Thr592 (Zhao & Guo, 2011 ) and ACC SYNTHASE 6 Ser480, Ser483, and Ser488 (Liu & Zhang, 2004 ).…”
Section: Resultsmentioning
confidence: 99%
“…Protein phosphocodes refer to a set of phosphorylated residues of a protein that is “encoded” by a specific kinase(s) and/or “decoded” by specific signaling molecules ( 37 40 ). Both MAPKs and BIN2, a kinase that mediate brassinosteroid signaling and stomatal asymmetric cell division, suppress SPCH proteins, and they appear to “write” a similar code on SPCH, at least within its MPKTD region ( 22 , 26 , 41 ).…”
Section: Discussionmentioning
confidence: 99%