Umlauf David, Goto Yuji, Feil Robert
Institute for Molecular Genetics CNRS UMR-5535 and University of Montpellier II, France.
Methods Mol Biol. 2004;287:99-120. doi: 10.1385/1-59259-828-5:099.
Covalent modifications on the nucleosomal histones are essential in chromatin regulation and gene expression. Patterns of histone modifications may be somatically maintained and can thereby maintain locus-specific repression/activity in defined lineages or throughout development. During recent years, histone acetylation and methylation have emerged as key players in the repression or activation of genes and chromosomal domains. Histone methylation and acetylation patterns (and other histone modifications) can be analyzed by chromatin immunoprecipitation (ChIP). This chapter describes how ChIP can be performed on native chromatin prepared from cells and tissues, in order to analyze histone methylation and acetylation at specific sites in the genome. We also present different PCR-based assays that can be applied to analyze loci of interest in immunoprecipitated chromatin fractions.
核小体组蛋白上的共价修饰在染色质调控和基因表达中至关重要。组蛋白修饰模式可能会在体细胞中得以维持,从而在特定谱系或整个发育过程中维持位点特异性的抑制/活性。近年来,组蛋白乙酰化和甲基化已成为基因和染色体结构域抑制或激活的关键因素。组蛋白甲基化和乙酰化模式(以及其他组蛋白修饰)可通过染色质免疫沉淀(ChIP)进行分析。本章描述了如何对从细胞和组织中制备的天然染色质进行ChIP,以便分析基因组中特定位点的组蛋白甲基化和乙酰化。我们还介绍了不同的基于PCR的检测方法,可用于分析免疫沉淀染色质组分中感兴趣的位点。