Amort Thomas, Sun Xueguang, Khokhlova-Cubberley Daria, Lusser Alexandra
Division of Molecular Biology, Biocenter, Medical University of Innsbruck, Innrain 80-82, Innsbruck, 6020, Austria.
Zymo Research Corp, Irvine, CA, USA.
Methods Mol Biol. 2017;1562:123-142. doi: 10.1007/978-1-4939-6807-7_9.
While low-throughput RNA bisulfite sequencing is the method of choice to assess the methylation status of specific cytosines in candidate RNAs, the combination of bisulfite treatment of RNA with today's high-throughput sequencing techniques opens the door to methylation studies at nucleotide resolution on a transcriptome-wide scale. Below we describe a protocol for the transcriptome-wide analysis of total or fractionated poly(A)RNA in cells and tissues. Although the nature of the bisulfite sequencing protocol makes it comparably easy to translate from a low to a high-throughput approach, several critical points require attention before starting such a project. We describe a step-by-step protocol for planning and performing the experiment and analyzing the data.
虽然低通量RNA亚硫酸氢盐测序是评估候选RNA中特定胞嘧啶甲基化状态的首选方法,但将RNA亚硫酸氢盐处理与当今的高通量测序技术相结合,为在全转录组范围内以核苷酸分辨率进行甲基化研究打开了大门。下面我们描述一种用于细胞和组织中总poly(A)RNA或分级分离的poly(A)RNA全转录组分析的方案。尽管亚硫酸氢盐测序方案的性质使其相对容易从低通量方法转换为高通量方法,但在启动此类项目之前,有几个关键点需要注意。我们描述了一个用于规划、进行实验和分析数据的分步方案。