The low oxygen, oxidative and osmotic stress responses synergistically act through the ethylene response factor VII genes RAP2.12, RAP2.2 and RAP2.3

• Published in: The Plant journal : for cell and molecular biology 2015-06, Vol.82 (5), p.772-784
• Main Authors: Papdi, Csaba, Pérez‐Salamó, Imma, Joseph, Mary Prathiba, Giuntoli, Beatrice, Bögre, László, Koncz, Csaba, Szabados, László
• Format: Article
• Language: English
• Subjects: Abscisic acid; Abscisic Acid - metabolism; Abscisic Acid - pharmacology; Acclimatization; anoxia; Arabidopsis - drug effects; Arabidopsis - physiology; Arabidopsis Proteins - genetics; Arabidopsis Proteins - metabolism; Arabidopsis thaliana; Botany; Carrier Proteins - genetics; Carrier Proteins - metabolism; DNA-Binding Proteins; Ethylene; ethylene response factor; Ethylenes - metabolism; Gene Expression Regulation, Plant; Genes; luciferase reporter; Mutation; osmotic and oxidative stress; Osmotic Pressure; Oxidative Stress; Oxygen; Oxygen - metabolism; Plants, Genetically Modified; Protein Structure, Tertiary; Proteins; RAP2; SINAT; Transcription factors; Transcription Factors - genetics; Transcription Factors - metabolism; Ubiquitin-Protein Ligases - metabolism
• ISSN: 0960-7412; 1365-313X
• DOI: 10.1111/tpj.12848

Summary The ethylene response factor VII (ERF‐VII) transcription factor RELATED TO APETALA2.12 (RAP2.12) was previously identified as an activator of the ALCOHOL DEHYDROGENASE1 promoter::luciferase (ADH1‐LUC) reporter gene. Here we show that overexpression of RAP2.12 and its homologues RAP2.2 and RAP2.3 sustains ABA‐mediated activation of ADH1 and activates hypoxia marker genes under both anoxic and normoxic conditions. Inducible expression of all three RAP2s conferred tolerance to anoxia, oxidative and osmotic stresses, and enhanced the sensitivity to abscisic acid (ABA). Consistently, the rap2.12‐2 rap2.3‐1 double mutant showed hypersensitivity to both submergence and osmotic stress. These findings suggest that the three ERF‐VII‐type transcription factors play roles in tolerance to multiple stresses that sequentially occur during and after submergence in Arabidopsis. Oxygen‐dependent degradation of RAP2.12 was previously shown to be mediated by the N‐end rule pathway. During submergence the RAP2.12, RAP2.2 and RAP2.3 are stabilized and accumulates in the nucleus affecting the transcription of stress response genes. We conclude that the stabilized RAP2 transcription factors can prolong the ABA‐mediated activation of a subset of osmotic responsive genes (e.g. ADH1). We also show that RAP2.12 protein level is affected by the REALLY INTERESTING GENE (RING) domain containing SEVEN IN ABSENTIA of Arabidopsis thaliana 2 (SINAT2). Silencing of SINAT1/2 genes leads to enhanced RAP2.12 abundance independently of the presence or absence of its N‐terminal degron. Taken together, our results suggest that RAP2.12 and its homologues RAP2.2 and RAP2.3 act redundantly in multiple stress responses. Alternative protein degradation pathways may provide inputs to the RAP2 transcription factors for the distinct stresses. Significance Statement The paper provides evidence that RAP2.12 and its homologs RAP2.2 and RAP2.3 act redundantly in multiple stress responses. Alternative protein degradation pathways may provide inputs to the RAP2 transcription factors for the distinct stresses.