Ethylene signaling promotes seed-derived somatic embryogenesis by directly activating LEAFY COTYLEDON 1 in...

As an important tool for plant regeneration, somatic embryogenesis (SE) exemplifies the remarkable plasticity and totipotency of plant cells. Auxin is a well-known initiator that drives the reprogramming of somatic cells into a pluripotent or totipotent state during somatic embryo formation. Accordingly, the auxin analog 2,4-dichlorophenoxyacetic acid (2,4-D) is the most widely applied hormone in SE induction media. Auxin and ethylene interact in many developmental processes, and ethylene signaling has been known for decades to be rapidly activated by auxin. However, the role of ethylene in SE remains elusive. In this study, we demonstrate that a series of Arabidopsis mutants with either enhanced or compromised ethylene signaling exhibit correspondingly higher or lower seed-derived SE induction rates under continuous 2,4-D treatment, respectively. Ethylene precursors, including 1-aminocyclopropane-1-carboxylic acid (ACC) and ethephon (ETH), promoted SE induction, whereas the ethylene perception inhibitor 1-methylcyclopropene (1-MCP) suppressed it. These results indicate that ethylene response is essential for auxin-mediated SE. Molecular and histological analyses revealed that auxin rapidly activates the transcription of key ethylene biosynthesis genes, such as ACC SYNTHASE (ACS) and ACC OXIDASE 2 (ACO2), leading to enhanced ethylene responses during early SE. Furthermore, we found that the core ethylene transcription factors ETHYLENE-INSENSITIVE3 (EIN3) and EIN3-LIKE 1 (EIL1) directly bind to the promoters of the embryonic identity genes LEAFY COTYLEDON 1 (LEC1) and LEC2, and that ethylene signaling positively regulates LEC1 transcription. Taken together, our results demonstrate that ethylene signaling promotes auxin-mediated SE through direct upregulation of LEC1 expression.