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使用甲基化敏感扩增多态性(MSAP)分析DNA胞嘧啶甲基化模式

Analysis of DNA Cytosine Methylation Patterns Using Methylation-Sensitive Amplification Polymorphism (MSAP).

作者信息

Guevara María Ángeles, de María Nuria, Sáez-Laguna Enrique, Vélez María Dolores, Cervera María Teresa, Cabezas José Antonio

机构信息

Department of Forest Ecology and Genetic, Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria - Centro de InvestigaciónForestal (INIA-CIFOR), Ctra. de La Coruña Km 7,5, Madrid, 28040, Spain.

出版信息

Methods Mol Biol. 2017;1456:99-112. doi: 10.1007/978-1-4899-7708-3_9.

DOI:10.1007/978-1-4899-7708-3_9
PMID:27770361
Abstract

Different molecular techniques have been developed to study either the global level of methylated cytosines or methylation at specific gene sequences. One of them is the methylation-sensitive amplified polymorphism technique (MSAP) which is a modification of amplified fragment length polymorphism (AFLP). It has been used to study methylation of anonymous CCGG sequences in different fungi, plants, and animal species. The main variation of this technique resides on the use of isoschizomers with different methylation sensitivity (such as HpaII and MspI) as a frequent-cutter restriction enzyme. For each sample, MSAP analysis is performed using both EcoRI/HpaII- and EcoRI/MspI-digested samples. A comparative analysis between EcoRI/HpaII and EcoRI/MspI fragment patterns allows the identification of two types of polymorphisms: (1) methylation-insensitive polymorphisms that show common EcoRI/HpaII and EcoRI/MspI patterns but are detected as polymorphic amplified fragments among samples and (2) methylation-sensitive polymorphisms which are associated with the amplified fragments that differ in their presence or absence or in their intensity between EcoRI/HpaII and EcoRI/MspI patterns. This chapter describes a detailed protocol of this technique and discusses the modifications that can be applied to adjust the technology to different species of interest.

摘要

已经开发出不同的分子技术来研究甲基化胞嘧啶的整体水平或特定基因序列的甲基化情况。其中之一是甲基化敏感扩增多态性技术(MSAP),它是扩增片段长度多态性(AFLP)的一种改进。它已被用于研究不同真菌、植物和动物物种中匿名CCGG序列的甲基化。该技术的主要变化在于使用具有不同甲基化敏感性的同裂酶(如HpaII和MspI)作为常用切割限制酶。对于每个样本,使用EcoRI/HpaII和EcoRI/MspI消化的样本进行MSAP分析。EcoRI/HpaII和EcoRI/MspI片段模式之间的比较分析允许识别两种类型的多态性:(1)甲基化不敏感多态性,其显示常见的EcoRI/HpaII和EcoRI/MspI模式,但在样本中被检测为多态性扩增片段;(2)甲基化敏感多态性,其与在EcoRI/HpaII和EcoRI/MspI模式之间存在与否或强度不同的扩增片段相关。本章描述了该技术的详细方案,并讨论了可用于将该技术调整到不同目标物种的修改方法。

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