Pillai Smitha, Chellappan Srikumar P
Drug Discovery Program, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL, USA.
Methods Mol Biol. 2009;523:341-66. doi: 10.1007/978-1-59745-190-1_23.
Deregulation of transcriptional activity of many genes has been causatively linked to human diseases including cancer. Altered patterns of gene expression in normal and cancer cells are the result of inappropriate expression of transcription factors and chromatin-modifying proteins. Chromatin immunoprecipitation assay is a well-established tool for investigating the interactions between regulatory proteins and DNA at distinct stages of gene activation. ChIP coupled with DNA microarrays, known as ChIP on chip, allow us to determine the entire spectrum of in vivo DNA-binding sites for a given protein. This has been of immense value because ChIP on chip assays can provide a snapshot of the transcriptional regulatory mechanisms on a genome-wide scale. This article outlines the general strategies used to carry out ChIP-chip assays to study the differential recruitment of regulatory molecules based on the studies conducted in our lab as well as other published protocols.
许多基因转录活性的失调与包括癌症在内的人类疾病存在因果关联。正常细胞和癌细胞中基因表达模式的改变是转录因子和染色质修饰蛋白表达不当的结果。染色质免疫沉淀测定法是一种成熟的工具,用于研究基因激活不同阶段调控蛋白与DNA之间的相互作用。染色质免疫沉淀与DNA微阵列相结合,即所谓的芯片上的染色质免疫沉淀,使我们能够确定给定蛋白质在体内的DNA结合位点的整个谱图。这具有巨大的价值,因为芯片上的染色质免疫沉淀测定法可以在全基因组范围内提供转录调控机制的快照。本文根据我们实验室进行的研究以及其他已发表的方案,概述了用于进行芯片上的染色质免疫沉淀测定以研究调控分子差异募集的一般策略。