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焦磷酸测序法分析DNA甲基化

Analysis of DNA Methylation by Pyrosequencing.

作者信息

Delaney Colin, Garg Sanjay K, Yung Raymond

机构信息

Department of Internal Medicine, University of Michigan Medical School, 109 Zina Pitcher Place, Ann Arbor, MI, 48109, USA.

出版信息

Methods Mol Biol. 2015;1343:249-64. doi: 10.1007/978-1-4939-2963-4_19.

Abstract

Pyrosequencing is a technique that uses a sequencing-by-synthesis system which is designed to quantify single-nucleotide polymorphisms (SNPs). Artificial C/T SNP creation via bisulfite modification permits measurement of DNA methylation locally and globally in real time. Alteration in DNA methylation has been implicated in aging, as well as aging-related conditions such as cancer, as well as cardiovascular, neurodegenerative, and autoimmune diseases. Considering its ubiquitous presence in divergent clinical pathologies, quantitative analysis of DNA CpG methylation both globally and at individual genes helps to elucidate the regulation of genes involved in pathophysiological conditions. The ability to detect and quantify the methylation pattern of DNA has the potential to serve as an early detection marker and potential drug target for several diseases. Here, we provide a detailed technical protocol for pyrosequencing supplemented by critical information about assay design and nuances of the system that provides a strong foundation for beginners in the field.

摘要

焦磷酸测序是一种利用合成测序系统的技术,该系统旨在对单核苷酸多态性(SNP)进行定量分析。通过亚硫酸氢盐修饰人工创建C/T SNP,能够实时在局部和整体水平上测量DNA甲基化。DNA甲基化的改变与衰老以及与衰老相关的病症(如癌症)以及心血管疾病、神经退行性疾病和自身免疫性疾病有关。鉴于其在不同临床病理中的普遍存在,对DNA CpG甲基化进行整体和单个基因水平的定量分析有助于阐明参与病理生理状况的基因的调控机制。检测和定量DNA甲基化模式的能力有可能作为多种疾病的早期检测标志物和潜在的药物靶点。在此,我们提供了一份详细的焦磷酸测序技术方案,并辅以有关实验设计和系统细微之处的关键信息,为该领域的初学者提供了坚实的基础。

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Analysis of DNA Methylation by Pyrosequencing.焦磷酸测序法分析DNA甲基化
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