• ISSN 1008-505X
  • CN 11-3996/S

纳米氧化锌增强红树林“秋茄”抗寒性机制的转录组分析

Transcriptomic analysis of the mechanism underlying ZnO nanoparticle-improved cold tolerance in mangrove kandelia obovata

  • 摘要:
    目的 纳米氧化锌(ZnO NPs)具有提高作物抗寒的作用。我们研究了纳米氧化锌提高抗寒性的代谢路径,并研发了含有ZnO NPs的防冻剂,为我国最北缘红树林安全越冬提供理论和技术支撑。
    方法 以一年生红树林秋茄(Kandelia obovata)幼苗为试验材料进行了盆栽试验。秋茄幼苗首先在常温下分别喷施清水、200 mg/L ZnO NPs,然后,每个处理组分为两份,一份继续在常温(昼夜温度为25℃/20℃)下培养,另一份在昼/夜温度为8℃/-3℃的低温下胁迫处理3天,测定幼苗叶片的叶绿素荧光参数,收获后利用转录组测序技术分析影响秋茄抗寒能力的关键通路,采用DESeq2软件,以∣log2FC∣≥1和P-value < 0.05为阈值筛选差异表达基因(DEGs)。防冻剂效果盆栽试验设置常温下喷施清水对照、常规复合防冻剂(防冻剂)、含ZnO NPs的复合防冻剂(纳米氧化锌防冻剂)三个处理,然后在低温下胁迫处理4天,测定丙二醛含量、光合参数,剩余幼苗移回常温培养7天,记录各处理叶片受冻害情况。
    结果 与喷清水常温相比,低温胁迫显著降低了秋茄幼苗叶片PSII实际光化学量子产量(ΦPSII)、PSII最大光化学效率(Fv/Fm)光化学猝灭系数(qP)光适应状态下PSII最大光化学效率(Fv’/Fm’);喷ZnO_NPs低温胁迫处理下,秋茄幼苗叶片ΦPSIIFv/FmqPFv’/Fm’值分别为喷清水低温胁迫处理的2.26、2.33、2.40和1.71倍。喷清水低温胁迫与喷清水常温相比,共检测到7840个DEGs,其中上调基因4399个,下调基因3441个;喷施ZnO NPs低温胁迫与低温胁迫相比,共检测到7856个DEGs,其中上调基因3462个,下调基因4394个。所有处理间共鉴定到36043个差异表达基因,其主要富集于光合作用、核糖体结构与翻译、MAPK信号及苯丙烷代谢通路。与防冻剂处理相比,纳米氧化锌防冻剂处理显著降低了秋茄叶片相对电导率、丙二醛含量以及幼苗冻害指数,显著提高叶片净光合速率、气孔导度、蒸腾速率、CO2碳饱和点、羧化效率、最大光合能力,降低CO2补偿点,从而提高植株的光合固碳能力,减轻低温胁迫对秋茄幼苗的伤害。防冻剂也显著提高了低温胁迫净光合速率与羧化效率,显著抑制了MDA含量,并显示出一定的抗低温伤害效果。
    结论 ZnO NPs通过调控光合作用、核糖体结构与翻译、MAPK信号及苯丙烷代谢通路相关基因的表达,稳定细胞膜功能,维持光化学效率和固碳能力。含ZnO NPs的复合防冻剂较普通防冻剂可以进一步提高受低温胁迫的秋茄幼苗叶片光合气体交换和CO2固定能力,显著降低秋茄的冻害指数,这种增强效果与转录组分析中ZnO NPs预处理幼苗的抗寒分子机制相吻合。

     

    Abstract:
    Objectives Zinc oxide nanoparticles (ZnO NPs) have been shown to enhance crop cold tolerance. In this study, we investigated the metabolic pathways by which ZnO NPs improve cold tolerance and developed a ZnO NPs-containing antifreeze agent, aiming to provide theoretical and technical support for the safe overwintering of mangrove forests at the northern limit of their distribution in China.
    Methods One-year-old seedlings of the mangrove species Kandelia obovata were planted in pots. The seedlings were first sprayed with water or 200 mg/L ZnO NPs under normal temperature conditions (25oC/20oC day/night). The seedlings in each treatment group were divided into two subgroups: one subgroup was maintained under normal-temperature conditions, whereas the other was subjected to low-temperature stress (8oC /-3oC day/night) for 3 days, after which chlorophyll fluorescence parameters were measured. Leaves were then harvested for transcriptome sequencing to identify key pathways associated with cold tolerance in K. obovata. Differentially expressed genes (DEGs) were identified using DESeq2 with thresholds of |log2FC| ≥ 1 and P-value < 0.05. Subsequently, antifreeze-agent experiments were conducted using potted seedlings. The seedlings were divided into three groups: one sprayed with water, one sprayed with conventional antifreeze agent (Antifreeze agent), and the third sprayed with a ZnO NP-containing antifreeze agent of the same formulation. These seedlings were then subjected to cold stress for 4 days, after which photosynthetic parameters and malondialdehyde (MDA) content were measured in a subset of seedlings. The remaining seedlings were transferred to normal-temperature conditions for 7 days, and cold injury symptoms were evaluated.
    Results Compared with water-sprayed seedlings maintained under normal temperature conditions, seedlings subjected to low-temperature stress exhibited significant reductions in the actual photochemical quantum yield of PSII (ΦPSII), maximum photochemical efficiency of PSII (Fv/Fm), photochemical quenching coefficient (qP), and maximum efficiency of PSII in the light-adapted state (Fv’/Fm’). Under low-temperature stress, the ΦPSII, Fv/Fm, qP, and Fv’/Fm’ values of ZnO NP-treated seedlings were 2.26, 2.33, 2.40, and 1.71 times those of the water-sprayed low-temperature-stressed seedlings, respectively. A total of 7,840 DEGs were identified between the water-sprayed low-temperature-stressed and water-sprayed normal-temperature groups, including 4,399 up-regulated and 3,441 down-regulated genes. Similarly, a total of 7,856 DEGs were identified between the water-sprayed low-temperature-stressed group and the ZnO NP-sprayed low-temperature-stressed group, including 3,462 up-regulated and 4,394 down-regulated genes. Across all treatments, a total of 36,043 DEGs were identified, and these genes were primarily enriched in photosynthesis, ribosomal-related processes, MAPK signaling, and phenylpropanoid metabolism pathways. Compared with the antifreeze agent treatment group, the ZnO NP-containing antifreeze-agent group showed significant reductions in relative electrolyte conductivity, MDA content, and freezing injury index. This group also exhibited significantly increased net photosynthetic rate, stomatal conductance, transpiration rate, CO2 saturation point, carboxylation efficiency, and maximum photosynthetic capacity, while showing a decreased CO2 compensation point, thereby enhancing photosynthetic carbon assimilation and alleviating cold-induced injury. Furthermore, the antifreeze agent alone significantly increased net photosynthetic rate and carboxylation efficiency, reduced MDA content under cold stress, and provided partial protection against cold injury.
    Conclusions ZnO NPs stabilized cell membranes and maintained photochemical efficiency and carbon fixation capacity by regulating the expression of genes involved in photosynthesis, ribosomal-related processes, MAPK signaling, and phenylpropanoid metabolism. The ZnO NP-containing antifreeze agent can further enhance the photosynthetic gas exchange and CO2 fixation capacity of Kandelia obovata seedling leaves under low-temperature stress compared with ordinary antifreeze, and significantly reduce the freezing injury index of Kandelia obovata, consistent with the cold-tolerance mechanisms revealed by transcriptomic analysis of ZnO NP-pretreated seedlings.

     

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