A receptor-like protein mediates the response to pectin modification by activating brassinosteroid signaling - INRAE - Institut national de recherche pour l’agriculture, l’alimentation et l’environnement Accéder directement au contenu
Article Dans Une Revue Proceedings of the National Academy of Sciences of the United States of America Année : 2014

A receptor-like protein mediates the response to pectin modification by activating brassinosteroid signaling

Résumé

The brassinosteroid (BR) signaling module is a central regulator of plant morphogenesis, as indicated by the large number of BR-responsive cell wall-related genes and the severe growth defects of BR mutants. Despite a detailed knowledge of the signaling components, the logic of this auto-/paracrine signaling module in growth control remains poorly understood. Recently, extensive cross-talk with other signaling pathways has been shown, suggesting that the outputs of BR signaling, such as gene-expression changes, are subject to complex control mechanisms. We previously provided evidence for a role of BR signaling in a feedback loop controlling the integrity of the cell wall. Here, we identify the first dedicated component of this feedback loop: a receptor-like protein (RLP44), which is essential for the compensatory triggering of BR signaling upon inhibition of pectin de-methylesterification in the cell wall. RLP44 is required for normal growth and stress responses and connects with the BR signaling pathway, presumably through a direct interaction with the regulatory receptor-like kinase BAK1. These findings corroborate a role for BR in controlling the sensitivity of a feedback signaling module involved in maintaining the physico-chemical homeostasis of the cell wall during cell expansion.
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Dates et versions

hal-01204121 , version 1 (27-05-2020)

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Sebastian Wolf, Dieuwertje van Der Does, Friederike Ladwig, Carsten Sticht, Andreas Kolbeck, et al.. A receptor-like protein mediates the response to pectin modification by activating brassinosteroid signaling. Proceedings of the National Academy of Sciences of the United States of America, 2014, 111 (42), pp.15261-15266. ⟨10.1073/pnas.1322979111⟩. ⟨hal-01204121⟩
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