Embrapa Genetic Resources and Biotechnology, Brasília, DF, Brazil.
Methods Mol Biol. 2024;2827:323-350. doi: 10.1007/978-1-0716-3954-2_22.
This chapter describes a step-by-step protocol for rapid serological quantification of global DNA methylation by enzyme-linked immunosorbent assay (ELISA) in plant tissue culture specimens. As a case study model, we used the coconut palm (Cocos nucifera), from which plumules were subjected to somatic embryogenesis followed by embryogenic calli multiplication. DNA methylation is one of the most common epigenetic markers in the regulation of gene expression. DNA methylation is generally associated with non-expressed genes, that is, gene silencing under certain conditions, and the degree of DNA methylation can be used as a marker of various physiological processes, both in plants and in animal cells. Methylation consists of adding a methyl radical to carbon 5 of the DNA cytosine base. Herein, the global DNA methylation was quantified by ELISA with antibodies against methylated cytosines using a commercial kit (Zymo-Research™). The method allowed the detection of methylation in total DNA extracts from coconut palm embryogenic calli (arising from somatic embryogenesis) cultivated in liquid or solid media by using antibodies against methylated cytosines and enzymatic development with a colorimetric substrate. Control samples of commercially provided Escherichia coli bacterial DNA with previously known methylation percentages were included in the ELISA test to construct an experimental methylation standard curve. The logarithmic regression of this E. coli standard curve allowed methylation quantification in coconut palm samples. The present ELISA methodology, applied to coconut palm tissue culture specimens, is promising for use in other plant species and botanical families. This chapter is presented in a suitable format for use as a step-by-step laboratory procedure manual, with theoretical introduction information, which makes it easy to apply the protocol in samples of any biological nature to evaluate DNA global methylation associated with any physiological process.
这一章描述了一种通过酶联免疫吸附测定(ELISA)快速定量植物组织培养标本中整体 DNA 甲基化的分步协议。作为一个案例研究模型,我们使用椰子(Cocos nucifera),从椰苗进行体细胞胚胎发生,然后进行胚胎性愈伤组织增殖。DNA 甲基化是基因表达调控中最常见的表观遗传标记之一。DNA 甲基化通常与非表达基因相关,即在某些条件下基因沉默,并且 DNA 甲基化的程度可以用作各种生理过程的标志物,无论是在植物还是动物细胞中。甲基化包括在 DNA 胞嘧啶碱基的碳 5 上添加一个甲基自由基。在此,使用针对甲基化胞嘧啶的商业试剂盒(Zymo-Research™)通过 ELISA 定量测定椰子胚胎性愈伤组织(来自体细胞胚胎发生)的整体 DNA 甲基化。该方法允许使用针对甲基化胞嘧啶的抗体,通过酶促显色底物,在液体或固体培养基中培养的椰子胚胎性愈伤组织的总 DNA 提取物中检测甲基化。将具有先前已知甲基化百分比的商业提供的大肠杆菌细菌 DNA 的对照样品纳入 ELISA 测试中,以构建实验甲基化标准曲线。该大肠杆菌标准曲线的对数回归允许对椰子样品进行甲基化定量。应用于椰子组织培养标本的这种 ELISA 方法有望用于其他植物物种和植物科。本章以适合用作分步实验室程序手册的格式呈现,提供了理论介绍信息,使人们可以轻松地将该方案应用于任何生物学性质的样品中,以评估与任何生理过程相关的整体 DNA 甲基化。