Abstract
BACKGROUND: Oat (Avena sativa), an economically important cereal crop globally, is highly vulnerable to high-temperature stress, challenging its geographic distribution and grain production. However, the mechanisms underlying oat's response to heat stress remain pooly understood. RESULTS: A time-course transcriptome revealed significant enrichment in lipid metabolism pathways during heat stress, which was corroborated by metabolomic findings. Integrated co-expression network analysis and KEGG enrichment further underscored the critical role of lipid metabolism in oat's adaptive response to heat stress. Comprehensive lipidomic profiling of heat-stressed oat seedlings demonstrated a substantial increase in the proportion of neutral lipids, suggesting an evolutionarily conserved protective strategy. Synergistic transcriptional responses indicated that heat-induced triacylglycerol (TAG) accumulation primarily originated from extensive membrane lipid turnover rather than de novo fatty acid (FA) synthesis, with the Kennedy pathway serving as the dominant route for TAG production. Enhanced phospholipid hydrolysis, acyl editing, and endoplasmic reticulum-localized FA desaturation collectively contributed to TAG enrichment in polyunsaturated FAs. Additionally, elevated levels of phosphatidylglycerol (PG) and phosphatidylinositol (PI) in oat may confer adaptive benefits under heat stress. CONCLUSIONS: This study demonstrates that lipid metabolism critically regulates heat stress response in oat. The findings provide valuable target genes for genetic improvement in enhancing oat thermotolerance.