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简化代表性亚硫酸氢盐测序(RRBS)。

Reduced Representation Bisulfite Sequencing (RRBS).

机构信息

Department of Maternal-Fetal Biology, Research Institute, National Center for Child Health and Development, Setagaya, Tokyo, Japan.

Department of Obstetrics and Gynecology, The Jikei University School of Medicine, Minato, Tokyo, Japan.

出版信息

Methods Mol Biol. 2023;2577:39-51. doi: 10.1007/978-1-0716-2724-2_3.

Abstract

Reduced representation bisulfite sequencing (RRBS) enriches CpG-rich genomic regions using the MspI restriction enzyme-which cuts DNA at all CCGG sites, regardless of their DNA methylation status at the CG site-and enables the measurement of DNA methylation levels at 5% ~ 10% of all CpG sites in the mammalian genome. RRBS has been utilized in a large number of studies as a cost-effective method to investigate DNA methylation patterns, mainly at gene promoters and CpG islands. Here, we describe protocols for gel-free preparation of RRBS libraries, quality control, sequencing, and data analysis. Our protocols typically require nine cycles of polymerase chain reaction (PCR) amplification to obtain a sufficient amount of library for sequencing when 100 ng of genomic DNA is used as a starting material; moreover, it takes 3 days to complete library preparation and quality control procedures for up to eight samples.

摘要

简化代表性亚硫酸氢盐测序(RRBS)使用 MspI 限制性内切酶富集富含 CpG 的基因组区域 - 该酶在 CG 位点的 DNA 甲基化状态无关的情况下切割所有 CCGG 位点 - 并能够测量哺乳动物基因组中所有 CpG 位点的 5%~10%的 DNA 甲基化水平。RRBS 已被广泛应用于大量研究中,作为一种经济有效的方法来研究 DNA 甲基化模式,主要是在基因启动子和 CpG 岛。在这里,我们描述了无胶制备 RRBS 文库、质量控制、测序和数据分析的方案。当使用 100ng 基因组 DNA 作为起始材料时,我们的方案通常需要九轮聚合酶链反应(PCR)扩增来获得足够量的文库进行测序;此外,完成文库制备和质量控制程序最多需要 3 天,最多可处理 8 个样本。

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