Lelandais Gaëlle, Blugeon Corinne, Merhej Jawad
Institut Jacques Monod, CNRS UMR 7592, University of Paris Diderot, Paris, France.
Plateforme Génomique, Ecole Normale Supérieure, Institut de Biologie de l'ENS, IBENS, Paris, 75005, France.
Methods Mol Biol. 2016;1361:185-202. doi: 10.1007/978-1-4939-3079-1_11.
Chromatin immunoprecipitation (ChIP) followed by high-throughput sequencing (ChIPseq) is a powerful technique for the genome-wide location of protein DNA-binding sites. The ChIP experiment consists in treating living cells with a cross-linking agent to bind proteins to their DNA substrates. After fragmentation of DNA, specific fractions associated with a particular protein of interest are purified by immunoaffinity. They are next sequenced and identified on the reference genome using dedicated bioinformatics programs. Several technical aspects are important to obtain high-quality ChIPseq results. This includes the quality of antibodies, the sequencing protocols, the use of accurate controls and the careful choice of bioinformatics tools. We present here a general protocol to perform ChIPseq analyses in yeast species. This protocol has been optimized to identify target genes of specific transcription factors but can be used for any other DNA binding proteins.
染色质免疫沉淀(ChIP)结合高通量测序(ChIPseq)是一种用于全基因组定位蛋白质DNA结合位点的强大技术。ChIP实验包括用交联剂处理活细胞,使蛋白质与其DNA底物结合。DNA片段化后,通过免疫亲和纯化与特定目标蛋白质相关的特定部分。接下来对它们进行测序,并使用专门的生物信息学程序在参考基因组上进行识别。要获得高质量的ChIPseq结果,几个技术方面很重要。这包括抗体质量、测序方案、准确对照的使用以及生物信息学工具的谨慎选择。我们在此展示一种在酵母物种中进行ChIPseq分析的通用方案。该方案已针对鉴定特定转录因子的靶基因进行了优化,但可用于任何其他DNA结合蛋白。