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Oilseed rape (Brassica napus L.) is a crop plant characterized by a poor nitrogen (N) use efficiency that is mainly due to low N remobilization efficiency during the sequential leaf senescence of the vegetative stage. As a high leaf N remobilization efficiency was strongly linked to a high remobilization of proteins during leaf senescence of rapeseed, our objective was to identify senescence-associated protease activities implicated in the protein degradation. To reach this goal, leaf senescence processes and protease activities were investigated in a mature leaf becoming senescent in plants subjected to ample or low nitrate supply. The characterization of protease activities was performed by using in vitro analysis of RuBisCO degradation with or without inhibitors of specific protease classes followed by a protease activity profiling using activity-dependent probes. As expected, the mature leaf became senescent regardless of the nitrate treatment, and nitrate limitation enhanced the senescence processes associated with an enhanced degradation of soluble proteins. The characterization of protease activities revealed that: (i) aspartic proteases and the proteasome were active during senescence regardless of nitrate supply, and (ii) the activities of serine proteases and particularly cysteine proteases (Papain-like Cys proteases and vacuolar processing enzymes) increased when protein remobilization associated with senescence was accelerated by nitrate limitation. Short statement: Serine and particularly cysteine proteases (both PLCPs and VPEs) seem to play a crucial role in the efficient protein remobilization when leaf senescence of oilseed rape was accelerated by nitrate limitation.

Original publication

DOI

10.1016/j.plantsci.2016.02.011

Type

Journal article

Journal

Plant Sci

Publication Date

05/2016

Volume

246

Pages

139 - 153

Keywords

Brassica napus, Cysteine proteases, Nitrogen remobilization efficiency, Protease activity, Senescence-associated proteases, Soluble proteins, Brassica napus, Chromatography, Liquid, Hydrogen-Ion Concentration, Peptide Hydrolases, Plant Leaves, Plant Proteins, Proteasome Endopeptidase Complex, Proteolysis, Ribulose-Bisphosphate Carboxylase, Seasons, Seeds, Solubility, Tandem Mass Spectrometry, Up-Regulation, Vacuoles