Department of Biochemistry and Molecular Biology, College of Life Sciences, Nanjing Agricultural University, Nanjing 210095, China.
Department of Biochemistry and Molecular Biology, College of Life Sciences, Nanjing Agricultural University, Nanjing 210095, China.
Environ Pollut. 2020 Jan;256:113464. doi: 10.1016/j.envpol.2019.113464. Epub 2019 Oct 24.
Cadmium (Cd) is a toxic metal that contributes to human diseases such as pediatric cancer and cardiovascular dysfunction. Epigenetic modification caused by Cd exposure is the major factor in etiology of environmentally-relevant diseases. However, the underlying epigenetic mechanism for Cd uptake and accumulation in food crops, particularly those growing in Cd-contaminated environments, is largely unknown. This study investigated uncharacterized regulatory mechanisms and biological functions of global DNA hypomethylation at CG sites that are associated with gene expression for Cd detoxification and accumulation in the food crop rice. Mutation of the CG maintenance enzyme OsMET1 confers rice tolerance to Cd exposure. Genome-wide analysis of OsMET1 loss of function mutant Osmet1 and its wild type shows numerous loci differentially methylated and upregulated genes for Cd detoxification, transport and accumulation. We functionally identified a new locus for a putative cadmium tolerance factor (here termed as OsCTF) and demonstrated that Cd-induced DNA demethylation is the drive of OsCTF expression. The 3'-UTR of OsCTF is the primary site of DNA and histone (H3K9me2) demethylation, which is associated with higher levels of OsCTF transcripts detected in the Osmet1 and Ossdg714 mutant lines. Mutation of OsCTF in rice led to hypersensitivity to Cd and the Osctf line accumulated more Cd, whereas transfer of OsCTF back to the Osctf mutant completely restored the normal phenotype. Our work unveiled an important epigenetic mechanism and will help develop breeding crops that contribute to food security and better human health.
镉(Cd)是一种有毒金属,会导致儿童癌症和心血管功能障碍等人类疾病。镉暴露引起的表观遗传修饰是与环境相关疾病病因学的主要因素。然而,在食用作物中,尤其是在镉污染环境中生长的食用作物中,镉的摄取和积累的潜在表观遗传机制在很大程度上尚未被了解。本研究调查了与镉解毒和积累相关的 CG 位点全局 DNA 低甲基化的未被表征的调控机制和生物学功能,该基因在食用作物水稻中表达。CG 维持酶 OsMET1 的突变赋予水稻对镉暴露的耐受性。对 OsMET1 功能丧失突变体 Osmet1 及其野生型的全基因组分析显示,许多位点的 CG 甲基化程度不同,并且与镉解毒、转运和积累相关的基因表达上调。我们功能鉴定了一个新的镉耐受因子(称为 OsCTF)的新位点,并证实 Cd 诱导的 DNA 去甲基化是 OsCTF 表达的驱动力。OsCTF 的 3'-UTR 是 DNA 和组蛋白(H3K9me2)去甲基化的主要位点,与 Osmet1 和 Ossdg714 突变体中检测到的更高水平的 OsCTF 转录本相关。水稻中 OsCTF 的突变导致对 Cd 的超敏反应,而 Osctf 系积累更多的 Cd,而将 OsCTF 转移回 Osctf 突变体则完全恢复了正常表型。我们的工作揭示了一个重要的表观遗传机制,并将有助于开发有助于食品安全和人类健康的作物品种。