Fan Lixia, Zhang Bingchun, Ning Mingxiao, Quan Shuangjun, Guo Changying, Cui Kai, Chen Lu, Yan Mengmeng, Ren Xianfeng
Institute of Quality Standard and Testing Technology for Agro-products, Shandong Academy of Agricultural Sciences, Jinan, China.
Shandong Provincial Key Laboratory of Test Technology on Food Quality and Safety, Jinan, China.
Front Plant Sci. 2024 Sep 20;15:1448971. doi: 10.3389/fpls.2024.1448971. eCollection 2024.
The application of agricultural film mulching technology has significantly contributed to increasing crop yield and income, but the pollution caused by residual film has seriously affected agricultural production and the natural environment. Agricultural film is commonly employed to enhance the yield of peanuts; its use may lead to excessive dibutyl phthalate (DBP) residues in peanut kernels. But, limited investigations have been conducted on the regulatory mechanism of peanut leaves in response to DBP exposure throughout the entire growth period.
To bridge this knowledge gap, we investigated the differences in transcriptome and metabolome of peanut leaves under DBP stress.
According to visual observations, the results of morphological response showed that the growth of peanut plants was significantly inhibited from seedling to pod stage under DBP treatment. Transcriptomic analysis results showed that the genes AH19G05510 (LRR receptor-like serine threonine-protein kinase) and AH20G31870 (disease resistance), belonging to the FAR1 family and bZIP family respectively, may be key genes involved in the resistance to DBP stress throughout its growth stages. Metabolomic analysis results showed that during the initial stage of DBP stress, the key metabolites in peanut leaves response to stress were carboxylic acids and derivatives, as well as fatty acyls. As peanut growth progressed, flavonoids gradually became more prominent in the resistance to DBP stress. By integrating metabolomics and transcriptomics analysis, we have identified that purine metabolism during seedling and flowering stages, as well as the flavone and flavonol biosynthesis pathways during pod and maturity stages, played a crucial role in response to DBP stress.
These findings not only provide valuable key gene and metabolic information for studying anti-plasticizer pollution throughout the entire growth period of peanuts, but also offer reference for enhancing crop resistance to plasticizer pollution through genetic modification and metabolic regulation.
农用薄膜覆盖技术的应用对提高作物产量和收入做出了显著贡献,但残留薄膜造成的污染严重影响了农业生产和自然环境。农用薄膜常用于提高花生产量;其使用可能导致花生仁中邻苯二甲酸二丁酯(DBP)残留超标。但是,关于花生叶片在整个生长周期对DBP暴露的调控机制的研究较少。
为填补这一知识空白,我们研究了DBP胁迫下花生叶片的转录组和代谢组差异。
通过肉眼观察,形态学响应结果表明,在DBP处理下,花生植株从幼苗期到结荚期的生长受到显著抑制。转录组分析结果显示,分别属于FAR1家族和bZIP家族的基因AH19G05510(富含亮氨酸重复序列的类受体丝氨酸苏氨酸蛋白激酶)和AH20G31870(抗病性)可能是参与花生整个生长阶段对DBP胁迫抗性的关键基因。代谢组分析结果表明,在DBP胁迫初期,花生叶片响应胁迫的关键代谢产物是羧酸及其衍生物以及脂肪酰基。随着花生生长的推进,黄酮类化合物在对DBP胁迫的抗性中逐渐变得更加突出。通过整合代谢组学和转录组学分析,我们确定了幼苗期和开花期的嘌呤代谢以及结荚期和成熟期的黄酮和黄酮醇生物合成途径在响应DBP胁迫中起关键作用。
这些发现不仅为研究花生整个生长周期的抗增塑剂污染提供了有价值的关键基因和代谢信息,也为通过基因改造和代谢调控提高作物对增塑剂污染的抗性提供了参考。