State Key Laboratory of North China Crop Improvement and Regulation, College of Resources and Environmental Sciences, Hebei Agricultural University, Hebei, Baoding 071000, China; Key Laboratory for Farmland Eco-environment of Hebei Province, Hebei, Baoding 071000, China.
Key Laboratory of Vegetable Germplasm Innovation and Utilization of Hebei, Hebei Collaborative Innovation Center for Green and Efficient Vegetable Industry, College of Horticulture, Hebei, Baoding 071000, China.
J Hazard Mater. 2023 Feb 15;444(Pt A):130385. doi: 10.1016/j.jhazmat.2022.130385. Epub 2022 Nov 11.
Atmospheric fine particulate matter (PM) mainly contributes to Pb accumulation in the edible leaves of Chinese cabbage in North China. It was found that a low-Pb-accumulation (LPA) genotype of Chinese cabbage contained less Pb in leaves than high-Pb-accumulation (HPA) genotype exposed to PM-Pb. However, there are no data on the transcriptional regulatory mechanisms of foliar PM-Pb uptake by Chinese cabbage. The present study investigated the retention of PM-Pb in foliar apoplast and symplasm and the underlying molecular mechanisms of reduced Pb in LPA leaves. It appeared more Pb in apoplast and less Pb in symplasm of LPA leaves, whereas the pattern was opposite in HPA. There were 2646 and 3095 differentially expressed genes (DEGs) in LPA and HPA leaves under PM-Pb stress with clearly genotype-specific function, respectively. Furthermore, mRNA levels of XTH16 regulating cell wall thickening, PME2 and PME6 involved in cell wall remodification were significantly expressed in LPA, but not in HPA. Meanwhile, foliar PM-Pb stress downregulated expression of ZIP1, YSL1, and CNGC3 responsible for Pb influx to cell, and upregulated expression of ABCG36 regulated Pb efflux from symplasm in LPA leaves. These results improve our understanding to the mechanisms underlying foliar Pb uptake from PM-Pb at transcriptomic level.
大气细颗粒物(PM)主要导致中国大白菜可食用叶片中 Pb 的积累。研究发现,与暴露于 PM-Pb 的高 Pb 积累(HPA)基因型相比,大白菜的低 Pb 积累(LPA)基因型叶片中 Pb 含量较低。然而,目前还没有关于大白菜叶片对 PM-Pb 吸收的转录调控机制的数据。本研究调查了 PM-Pb 在叶片质外体和共质体中的保留情况,以及 LPA 叶片中 Pb 减少的潜在分子机制。LPA 叶片中 Pb 在外质体中较多,而在共质体中较少,而 HPA 叶片则相反。在 PM-Pb 胁迫下,LPA 和 HPA 叶片中分别有 2646 和 3095 个差异表达基因(DEGs),具有明显的基因型特异性功能。此外,XTH16 基因调节细胞壁增厚,PME2 和 PME6 基因参与细胞壁重塑,在 LPA 叶片中显著表达,但在 HPA 叶片中不表达。同时,叶片 PM-Pb 胁迫下调了负责 Pb 进入细胞的 ZIP1、YSL1 和 CNGC3 的表达,上调了 ABCG36 基因的表达,该基因负责从共质体中排出 Pb。这些结果提高了我们对叶片从 PM-Pb 中吸收 Pb 的转录组水平的理解。