The State Key Laboratory of Plant Cell and Chromosome Engineering, National Center for Plant Gene Research, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China.
Plant Physiol. 2012 Feb;158(2):790-800. doi: 10.1104/pp.111.190983. Epub 2011 Dec 19.
Cadmium (Cd) is toxic to plant cells. Under Cd exposure, the plant displayed leaf chlorosis, which is a typical symptom of iron (Fe) deficiency. Interactions of Cd with Fe have been reported. However, the molecular mechanisms of Cd-Fe interactions are not well understood. Here, we showed that FER-like Deficiency Induced Transcripition Factor (FIT), AtbHLH38, and AtbHLH39, three basic helix-loop-helix transcription factors involved in Fe homeostasis in plants, also play important roles in Cd tolerance. The gene expression analysis showed that the expression of FIT, AtbHLH38, and AtbHLH39 was up-regulated in the roots of plants treated with Cd. The plants overexpressing AtbHLH39 and double-overexpressing FIT/AtbHLH38 and FIT/AtbHLH39 exhibited more tolerance to Cd exposure than wild type, whereas no Cd tolerance was observed in plants overexpressing either AtbHLH38 or FIT. Further analysis revealed that co-overexpression of FIT with AtbHLH38 or AtbHLH39 constitutively activated the expression of Heavy Metal Associated3 (HMA3), Metal Tolerance Protein3 (MTP3), Iron Regulated Transporter2 (IRT2), and Iron Regulated Gene2 (IREG2), which are involved in the heavy metal detoxification in Arabidopsis (Arabidopis thaliana). Moreover, co-overexpression of FIT with AtbHLH38 or AtbHLH39 also enhanced the expression of NICOTIANAMINE SYNTHETASE1 (NAS1) and NAS2, resulting in the accumulation of nicotiananamine, a crucial chelator for Fe transportation and homeostasis. Finally, we showed that maintaining high Fe content in shoots under Cd exposure could alleviate the Cd toxicity. Our results provide new insight to understand the molecular mechanisms of Cd tolerance in plants.
镉(Cd)对植物细胞有毒。在 Cd 暴露下,植物表现出叶片黄化,这是铁(Fe)缺乏的典型症状。已经报道了 Cd 与 Fe 的相互作用。然而,Cd-Fe 相互作用的分子机制尚不清楚。在这里,我们表明,FER-样缺乏诱导转录因子(FIT)、AtbHLH38 和 AtbHLH39,这三个参与植物铁稳态的基本螺旋-环-螺旋转录因子,在 Cd 耐受中也发挥重要作用。基因表达分析表明,Cd 处理的植物根部 FIT、AtbHLH38 和 AtbHLH39 的表达上调。过表达 AtbHLH39 以及双过表达 FIT/AtbHLH38 和 FIT/AtbHLH39 的植物对 Cd 暴露的耐受性高于野生型,而过表达 AtbHLH38 或 FIT 的植物则没有 Cd 耐受性。进一步分析表明,FIT 与 AtbHLH38 或 AtbHLH39 的共过表达组成型激活 Heavy Metal Associated3(HMA3)、Metal Tolerance Protein3(MTP3)、Iron Regulated Transporter2(IRT2)和 Iron Regulated Gene2(IREG2)的表达,这些基因参与 Arabidopsis thaliana 中的重金属解毒。此外,FIT 与 AtbHLH38 或 AtbHLH39 的共过表达还增强了 NICOTIANAMINE SYNTHETASE1(NAS1)和 NAS2 的表达,导致尼克酰胺的积累,这是 Fe 运输和稳态的关键螯合剂。最后,我们表明在 Cd 暴露下维持地上部的高 Fe 含量可以减轻 Cd 毒性。我们的结果为理解植物 Cd 耐受的分子机制提供了新的见解。