Dahl John Arne, Collas Philippe
Institute of Basic Medical Sciences, Department of Biochemistry, Faculty of Medicine, University of Oslo, 0317 Oslo, Norway.
Nucleic Acids Res. 2008 Feb;36(3):e15. doi: 10.1093/nar/gkm1158. Epub 2008 Jan 17.
Chromatin immunoprecipitation (ChIP) is a powerful technique for studying protein-DNA interactions. Drawbacks of current ChIP assays however are a requirement for large cell numbers, which limits applicability of ChIP to rare cell samples, and/or lengthy procedures with limited applications. There are to date no protocols for fast and parallel ChIPs of post-translationally modified histones from small cell numbers or biopsies, and importantly, no protocol allowing for investigations of transcription factor binding in small cell numbers. We report here the development of a micro (micro) ChIP assay suitable for up to nine parallel quantitative ChIPs of modified histones or RNA polymerase II from a single batch of 1000 cells. MicroChIP can also be downscaled to monitor the association of one protein with multiple genomic sites in as few as 100 cells. MicroChIP is applicable to small fresh tissue biopsies, and a cross-link-while-thawing procedure makes the assay suitable for frozen biopsies. Using MicroChIP, we characterize transcriptionally permissive and repressive histone H3 modifications on developmentally regulated promoters in human embryonal carcinoma cells and in osteosarcoma biopsies. muChIP creates possibilities for multiple parallel and rapid transcription factor binding and epigenetic analyses of rare cell and tissue samples.
染色质免疫沉淀(ChIP)是研究蛋白质与DNA相互作用的一项强大技术。然而,当前ChIP检测方法的缺点是需要大量细胞,这限制了ChIP在稀有细胞样本中的应用,和/或程序冗长且应用有限。迄今为止,尚无从小细胞数量或活检样本中对翻译后修饰组蛋白进行快速并行ChIP的方案,重要的是,没有允许对小细胞数量中的转录因子结合进行研究的方案。我们在此报告了一种微量(micro)ChIP检测方法的开发,该方法适用于从一批1000个细胞中对修饰组蛋白或RNA聚合酶II进行多达九次并行定量ChIP。微量ChIP还可以缩小规模,以监测一种蛋白质与少至100个细胞中的多个基因组位点的关联。微量ChIP适用于小的新鲜组织活检样本,并且解冻时交联程序使该检测方法适用于冷冻活检样本。使用微量ChIP,我们对人胚胎癌细胞和骨肉瘤活检样本中发育调控启动子上的转录允许和抑制性组蛋白H3修饰进行了表征。微量ChIP为稀有细胞和组织样本的多重并行和快速转录因子结合及表观遗传分析创造了可能性。