トウモロコシ根の塩ストレス応答におけるN⁶-メチルアデノシン(m⁶A)メチル化を介した転写調節

Salt stress represents a significant abiotic factor that constrains maize growth. Epigenetic modifications play a crucial role in enabling plants to respond effectively to such stresses. Among these alterations, m⁶A methylation, which is the most common post-transcriptional modification of eukaryotic mRNA, shows dynamic variations that are closely linked to stress responses. In this study, we conducted a transcriptome-wide m⁶A methylation analysis on maize roots from the inbred line PH4CV, following treatment with 180 mM NaCl. The results identified 1309 differentially m⁶A methylated peaks (DMPs) and 2761 differentially expressed genes (DEGs) under salt stress conditions. Association analysis revealed that 179 DEGs contain DMPs. Key pathways involved in stress responses, including Ca²⁺ signaling transduction and ABA signaling, as well as ion homeostasis regulation (involving AKT, HKT, and other families) and the reactive oxygen species scavenging system (including POD, SOD, and CAT), play crucial roles in coping with salt stress. Furthermore, we identified a total of 26 m⁶A-related genes, comprising 7 eraser genes, 10 reader genes, and 9 writer genes. Notably, several key salt-responsive genes, such as RBOHB, AKT1, HKT1, and POD12, are correlated with m⁶A modification. This study provides a comprehensive map of m⁶A methylation dynamics in maize roots under salt stress, laying a foundational resource for future investigations into the epigenetic regulation of salt tolerance in maize.