Abstract

Abscisic acid (ABA) regulates diverse aspects of plant growth and secondary metabolism, yet its concentration-dependent effects on rhizomatous spice crops remain poorly understood at the systems level. Here, we investigated the phenotypic, physiological, hormonal, and multi-omics responses of ginger (Zingiber officinale) to foliar-applied ABA across a concentration gradient. Exogenous ABA modulated ginger growth in a distinctly non-linear manner. Low-to-moderate concentrations (5–15 mg/L) significantly enhanced aboveground branching and belowground rhizome yield, whereas high concentration (35 mg/L) inhibited branching while promoting structural carbohydrate accumulation, revealing a concentration-dependent trade-off between growth and secondary wall deposition. Hormone profiling uncovered global reprogramming of the endogenous hormonal network, with optimal ABA (15 mg/L) coordinately elevating growth-promoting hormones and defense-related signals, while high concentrations suppressed multiple hormone pathways and triggered negative feedback inhibition of endogenous ABA biosynthesis. Integrated metabolomic and transcriptomic analyses identified convergent enrichment on phenylpropanoid biosynthesis, gingerol biosynthesis, and plant hormone signal transduction. Co-expression network analysis revealed a highly interconnected module of 583 genes linking hormone signaling to secondary metabolism, with coordinated up-regulation of key enzymes from phenylalanine ammonia-lyase (PAL) to polyketide synthase under 15 mg/L ABA explaining the 64% increase in 6-gingerol content. This study establishes a mechanistic chain from ABA perception to improved ginger yield and quality, mediated by hormonal crosstalk and transcriptional activation of the phenylpropanoid-gingerol network. We propose an “ABA optimization window” of 5–15 mg/L for precision cultivation of high-quality ginger, providing a systems-level framework for understanding hormone-mediated regulation of secondary metab