Liu Shuo, Bao Yu, Deng Hui, Liu Guanqing, Han Yangshuo, Wu Yuechao, Zhang Tao, Chen Chen
Jiangsu Key Laboratory of Crop Genomics and Molecular Breeding/Jiangsu Key Laboratory of Crop Genetics and Physiology, Agricultural College of Yangzhou University, Yangzhou, 225009, China.
Jiangsu Co-Innovation Center for Modern Production Technology of Grain Crops, Yangzhou University, Yangzhou, 225009, China.
Rice (N Y). 2022 Jul 2;15(1):35. doi: 10.1186/s12284-022-00580-6.
DNA methylation is a conserved epigenetic modification which is vital for regulating gene expression and maintaining genome stability in both mammals and plants. Homozygous mutation of rice methyltransferase 1 (met1) gene can cause host death in rice, making it difficult to obtain plant material needed for hypomethylation research. To circumvent this challenge, the methylation inhibitor, 5-Aza-2'-deoxycytidine (AzaD), is used as a cytosine nucleoside analogue to reduce genome wide hypomethylation and is widely used in hypomethylation research. However, how AzaD affects plant methylation profiles at the genome scale is largely unknown. Here, we treated rice seedlings with AzaD and compared the AzaD treatment with osmet1-2 mutants, illustrating that there are similar CG hypomethylation and distribution throughout the whole genome. Along with global methylation loss class I transposable elements (TEs) which are farther from genes compared with class II TEs, were more significantly activated, and the RNA-directed DNA Methylation (RdDM) pathway was activated in specific genomic regions to compensate for severe CG loss. Overall, our results suggest that AzaD is an effective DNA methylation inhibitor that can influence genome wide methylation and cause a series of epigenetic variations.
DNA甲基化是一种保守的表观遗传修饰,对调节哺乳动物和植物的基因表达以及维持基因组稳定性至关重要。水稻甲基转移酶1(met1)基因的纯合突变会导致水稻宿主死亡,这使得获取低甲基化研究所需的植物材料变得困难。为了应对这一挑战,甲基化抑制剂5-氮杂-2'-脱氧胞苷(AzaD)被用作胞嘧啶核苷类似物以降低全基因组低甲基化,并广泛应用于低甲基化研究。然而,AzaD如何在基因组规模上影响植物甲基化图谱在很大程度上尚不清楚。在此,我们用AzaD处理水稻幼苗,并将AzaD处理与osmet1-2突变体进行比较,结果表明在整个基因组中存在相似的CG低甲基化及其分布。随着全基因组甲基化的丧失,与II类转座元件相比距离基因更远的I类转座元件(TEs)被更显著地激活,并且RNA指导的DNA甲基化(RdDM)途径在特定基因组区域被激活以补偿严重的CG缺失。总体而言,我们的结果表明AzaD是一种有效的DNA甲基化抑制剂,可影响全基因组甲基化并导致一系列表观遗传变异。