FtsH2-Dependent Proteolysis of EXECUTER1 Is Essential in Mediating Singlet Oxygen-Triggered Retrograde Signaling in Arabidopsis thaliana

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Photosystem II reaction center (PSII RC) and light-harvesting complex inevitably generate highly reactive singlet oxygen (¹O₂) that can impose photo-oxidative damage, especially when the rate of generation exceeds the rate of detoxification. Besides being toxic, ¹O₂ has also been ascribed to trigger retrograde signaling, which leads to nuclear gene expression changes. Two distinctive molecular components appear to regulate ¹O₂ signaling: a volatile signaling molecule β-cyclocitral (β-CC) generated upon oxidation of β-carotene by ¹O₂ in PSII RC assembled in grana core, and a thylakoid membrane-bound FtsH2 metalloprotease that promotes ¹O₂-triggered signaling through the proteolysis of EXECUTER1 (EX1) proteins associated with PSII in grana margin. The role of FtsH2 protease in ¹O₂ signaling was established recently in the conditional fluorescent (flu) mutant of Arabidopsis thaliana that generates ¹O₂ upon dark-to-light shift. The flu mutant lacking functional FtsH2 significantly impairs ¹O₂-triggered and EX1-mediated cell death. In the present study, the role of FtsH2 in the induction of ¹O₂ signaling was further clarified by analyzing the FtsH2-dependent nuclear gene expression changes in the flu mutant. Genome-wide transcriptome analysis showed that the inactivation of FtsH2 repressed the majority (85%) of the EX1-dependent ¹O₂-responsive genes (SORGs), providing direct connection between FtsH2-mediated EX1 degradation and ¹O₂-triggered gene expression changes. Furthermore, the overlap between β-CC-induced genes and EX1-FtsH2-dependent genes was very limited, further supporting the coexistence of two distinctive ¹O₂ signaling pathways.