Salvia miltiorrhiza-derived carbon dots enhance heat and cold stress tolerance through BrSPL11.1-mediated ascorbic acid biosynthesis and recycling pathways in flowering Chinese cabbage

丹参 抗坏血酸 活性氧 生物合成 抗氧化剂 氧化应激 植物 基因沉默 代谢途径 抑制因子 化学 转录因子 甲戊酸途径 细胞生物学 发起人 基因表达 光合作用 生物化学 生物途径 信号转导 基因
作者
Jiajing Zeng,Juan Li,Pengli Wang,Di Lu,Min Zhong,Yunyan Kang,Juxian Guo,Xian Yang
出处
期刊:Horticultural Plant Journal [KeAi]
标识
DOI:10.1016/j.hpj.2025.08.008
摘要

Salvia miltiorrhiza -derived carbon dots ( Sm CDs) have a potent antioxidant capacity. Squamosa promoter-binding protein-like (SPL) transcription factors respond to both heat and cold stress. However, the molecular mechanisms underlying the regulation of both high temperature (HT) and low temperature (LT) stress by Sm CDs through SPL-mediated ascorbate (AsA) biosynthesis and recycling pathways remain unexplored. Therefore, we systematically identified 29 BrSPLs and 16 genes related to AsA biosynthesis and recycling pathways in flowering Chinese cabbage. BrSPL11.1 and three genes ( BrGalDH , BrAPX , and BrDHAR1 ) involved in AsA biosynthesis and recycling pathways were induced by both HT and LT, and their expression patterns were modulated by Sm CDs. Functional analyses revealed that the expression of BrGalDH , BrAPX , and BrDHAR1 was suppressed in BrSPL11.1 overexpressing ( BrSPL11.1- OE) plants, leading to reduced AsA content and reactive oxygen species (ROS) accumulation, as well as enhanced sensitivity to thermal extremes. Conversely, atspl11.1 showed inverse phenotypic and biochemical trends. BrSPL11.1 directly bound to the promoters of BrGalDH , BrAPX , or BrDHAR1 and suppressed their transcription. Silencing BrGalDH , BrAPX , or BrDHAR1 decreased the AsA content and increased ROS accumulation, decreasing HT and LT resistance. Sm CD application effectively elevated the AsA content and attenuated ROS accumulation, alleviating oxidative damage under both stress conditions. Our results established that BrSPL11.1 acts as a dual-temperature stress repressor and that Sm CDs enhance HT and LT resistance by regulating BrSPL11.1-mediated AsA biosynthesis and recycling pathways.
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