1 Division of Biochemistry, ICAR-Indian Agricultural Research Institute, New Delhi, India.
2 ICAR-National Research Centre on Plant Biotechnology, New Delhi, India.
DNA Cell Biol. 2019 Jun;38(6):510-520. doi: 10.1089/dna.2018.4584. Epub 2019 Apr 24.
Plants, being sessile organisms, have evolved several dynamic mechanisms of gene regulation. Epigenetic modification especially cytosine methylation and demethylation actively regulates the expression of genes. To understand the role of cytosine methylation during isoflavonoid biosynthesis and accumulation, we performed cytosine methylation analysis in the coding region of two isoforms and gene, in two contrasting soybean genotypes differing in total isoflavone content (NRC37: high isoflavone; and NRC7: low isoflavone). The results indicated increased 5-mC in both the isoforms in NRC37 (∼20.51% in and ∼85% in ) compared with NRC7 (∼7.8% in and ∼2.5% in ) genotype, which signifies the positive role of 5-mC in the coding region of the gene leading to enhanced expression. In addition, temporal expression profiling [35 days after flowering (DAF), 45, 55, and 65 DAF] of both the isoforms showed increasing trend of accumulation in both the genotypes with maximum in NRC37 at 65 DAF. To further establish a correlation between methylation and expression of transcripts, we quantified the different isoforms of isoflavone in both the genotypes across all the stages. Therefore, the finding of this study would certainly increase our understanding of epigenetic regulation of isoflavone biosynthetic pathway mediated by the cytosine methylation that would assist molecular breeders to get high-performing soybean genotypes with better isoflavone yield.
植物作为固着生物,已经进化出几种动态的基因调控机制。表观遗传修饰,特别是胞嘧啶甲基化和去甲基化,积极调节基因的表达。为了了解胞嘧啶甲基化在异黄酮生物合成和积累过程中的作用,我们对两个异黄酮基因的编码区 和 进行了胞嘧啶甲基化分析,这两个基因在总异黄酮含量上存在差异(NRC37:高异黄酮;NRC7:低异黄酮)。结果表明,与 NRC7 ( 和 分别为 7.8%和 2.5%)相比,NRC37 中两个异构体的 5-mC 均增加( 和 分别为 20.51%和 85%),这表明 5-mC 在基因编码区的积极作用导致了基因表达的增强。此外,两个异构体的时间表达谱(开花后 35 天(DAF)、45、55 和 65 DAF)显示,在两个基因型中,积累呈增加趋势,在 NRC37 中最大,在 65 DAF 时达到最大值。为了进一步建立甲基化与转录物表达之间的相关性,我们在所有阶段都对两个基因型中的不同异黄酮异构体进行了定量分析。因此,本研究的发现必将提高我们对异黄酮生物合成途径的表观遗传调控的理解,这将有助于分子育种家获得具有更高异黄酮产量的高性能大豆基因型。