| Literature DB >> 30823989 |
Mélanie Ormancey1, Patrice Thuleau2, Renier A L van der Hoorn3, Sabine Grat4, Ambroise Testard5, Khaled Y Kamal6, Marie Boudsocq7, Valérie Cotelle8, Christian Mazars9.
Abstract
It is now well established that sphingoid Long Chain Bases (LCBs) are crucial mediators of programmed cell death. In plants, the mycotoxin fumonisin B1 (FB1) produced by the necrotrophic fungus Fusarium moniliforme disrupts the sphingolipid biosynthesis pathway by inhibiting the ceramide synthase leading to an increase in the amount of phytosphingosine (PHS) and dihydrosphingosine (DHS), the two major LCBs in Arabidopsis thaliana. To date, the signaling pathway involved in FB1-induced cell death remains largely uncharacterized. It is also well acknowledged that plant proteases such as papain-like cysteine protease are largely involved in plant immunity. Here, we show that the papain-like cysteine protease RD21 (responsive-to-desiccation-21) is activated in response to PHS and FB1 in Arabidopsis cultured cells and leaves, respectively. Using two allelic null mutants of RD21, and two different PCD bioassays, we demonstrate that the protein acts as a negative regulator of FB1-induced cell death in Arabidopsis.Entities:
Keywords: Activity-based protein profiling; Fumonisin B1; Papain-like cysteine proteases; Programmed cell death; RD21; Sphingolipids
Mesh:
Substances:
Year: 2018 PMID: 30823989 DOI: 10.1016/j.plantsci.2018.10.028
Source DB: PubMed Journal: Plant Sci ISSN: 0168-9452 Impact factor: 4.729