Barrilleaux Bonnie L, Cotterman Rebecca, Knoepfler Paul S
Department of Cell Biology and Human Anatomy, Institute of Pediatric Regenerative Medicine, University of California Davis School of Medicine, USA.
Methods Mol Biol. 2013;1012:117-33. doi: 10.1007/978-1-62703-429-6_9.
Myc and N-Myc have widespread impacts on the chromatin state within cells, both in a gene-specific and genome-wide manner. Our laboratory uses functional genomic methods including chromatin immunoprecipitation (ChIP), ChIP-chip, and, more recently, ChIP-seq to analyze the binding and genomic location of Myc. In this chapter, we describe an effective ChIP protocol using specific validated antibodies to Myc and N-Myc. We discuss the application of this protocol to several types of stem and cancer cells, with a focus on aspects of sample preparation prior to library preparation that are critical for successful Myc ChIP assays. Key variables are discussed and include the starting quantity of cells or tissue, lysis and sonication conditions, the quantity and quality of antibody used, and the identification of reliable target genes for ChIP validation.
Myc和N-Myc对细胞内的染色质状态具有广泛影响,这种影响在基因特异性和全基因组层面均有体现。我们实验室使用包括染色质免疫沉淀(ChIP)、ChIP芯片以及最近的ChIP测序等功能基因组学方法来分析Myc的结合情况和基因组定位。在本章中,我们描述了一种使用经过验证的针对Myc和N-Myc的特异性抗体的有效ChIP实验方案。我们讨论了该方案在几种类型的干细胞和癌细胞中的应用,重点关注文库制备前样本制备的各个方面,这些方面对于成功的Myc ChIP分析至关重要。文中讨论了关键变量,包括细胞或组织的起始量、裂解和超声处理条件、所用抗体的量和质量,以及用于ChIP验证的可靠靶基因的鉴定。