Metabolic control of arginine and ornithine levels paces the progression of leaf senescence.

Helena Janečková, Olivier Keech, Hongwei Guo, Per Gardeström, Thomas Moritz, Hans Stenlund, Nicolas Delhomme, Pernilla Lindén, Bastiaan Brouwer, Daniela Liebsch, Simon R Law, Xing Wen, Clément Boussardon, Daria Chrobok, Agnieszka Ziolkowska, Hou-Ling Wang, Zhonghai Li, Marta Juvany

Journal: Plant physiology 2022;189(4):1943-1960

PMID: 35604104

Abstract

Leaf senescence can be induced by stress or aging, sometimes in a synergistic manner. It is generally acknowledged that the ability to withstand senescence-inducing conditions can provide plants with stress resilience. Although the signaling and transcriptional networks responsible for a delayed senescence phenotype, often referred to as a functional stay-green trait, have been actively investigated, very little is known about the subsequent metabolic adjustments conferring this aptitude to survival. First, using the individually darkened leaf (IDL) experimental setup, we compared IDLs of wild-type (WT) Arabidopsis (Arabidopsis thaliana) to several stay-green contexts, that is IDLs of two functional stay-green mutant lines, oresara1-2 (ore1-2) and an allele of phytochrome-interacting factor 5 (pif5), as well as to leaves from a WT plant entirely darkened (DP). We provide compelling evidence that arginine and ornithine, which accumulate in all stay-green contexts-likely due to the lack of induction of amino acids (AAs) transport-can delay the progression of senescence by fueling the Krebs cycle or the production of polyamines (PAs). Secondly, we show that the conversion of putrescine to spermidine (SPD) is controlled in an age-dependent manner. Thirdly, we demonstrate that SPD represses senescence via interference with ethylene signaling by stabilizing the ETHYLENE BINDING FACTOR1 and 2 (EBF1/2) complex. Taken together, our results identify arginine and ornithine as central metabolites influencing the stress- and age-dependent progression of leaf senescence. We propose that the regulatory loop between the pace of the AA export and the progression of leaf senescence provides the plant with a mechanism to fine-tune the induction of cell death in leaves, which, if triggered unnecessarily, can impede nutrient remobilization and thus plant growth and survival.

© The Author(s) 2022. Published by Oxford University Press on behalf of American Society of Plant Biologists.

Address: Umeå Plant Science Centre, Department of Plant Physiology, Umeå University, S-90187 Umeå, Sweden.; National Engineering Laboratory for Tree Breeding, College of Biological Sciences and Technology, Beijing Forestry University, Beijing 100083, China.; Department of Biology, Institute of Plant and Food Science, Southern University of Science and Technology (SUSTech), Shenzhen, Guangdong 518055, China.; Centre of the Region Haná for Biotechnological and Agricultural Research, Department of Biophysics, Faculty of Science, Palacký University, 783 71 Olomouc, Czech Republic.; Department of Forest Genetics and Plant Physiology, Umeå Plant Science Centre, Swedish University of Agricultural Sciences, S-901 83 Umeå, Sweden.; Novo Nordisk Centre for Basic Metabolic Research, University of Copenhagen, D-2200 Copenhagen N, Denmark.
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