Nagarajan Usha, Pakkiriswami Shanmugasundaram
Department of Biochemistry, Central University of Haryana, Mahendergarh, Haryana, India.
Department of Medicine (Cardiovascular Division), Medical School, Lillehei Heart Institute, University of Minnesota, Minneapolis, MN, USA.
Methods Mol Biol. 2025;2889:181-192. doi: 10.1007/978-1-0716-4322-8_13.
Homeobox genes (HOX), the master regulators, deploy a unique set of target genes to coordinate and orchestrate the spatiotemporal development of an organism. HOX encoded transcriptional factors regulate the expression of target genes by binding to the specific sequences on the genome. Chromatin Immunoprecipitation (ChIP) and Chromatin Immunoprecipitation with Sequencing (ChIP-Seq) are widely used to map and understand specific gene locus and global regulatory regions on the genome. ChIP is a powerful technique of cross-linking the proteins bound to the DNA, fragmenting DNA to the desired size, and pulling them down using specific antibodies to enrich and analyze the protein-bound DNA. Based on the mapping information, a differential ChIP can be performed to understand cis-regulatory modulations at a defined locus by two developmental stages. This chapter describes the differential ChIP used to identify new targets by comparing two different developmental stages simultaneously using Drosophila melanogaster.
同源框基因(HOX)作为主要调控因子,通过部署一组独特的靶基因来协调和编排生物体的时空发育。HOX编码的转录因子通过与基因组上的特定序列结合来调控靶基因的表达。染色质免疫沉淀(ChIP)和染色质免疫沉淀测序(ChIP-Seq)被广泛用于绘制和理解基因组上的特定基因座和全局调控区域。ChIP是一种强大的技术,可将与DNA结合的蛋白质进行交联,将DNA片段化至所需大小,然后使用特异性抗体将其拉下,以富集和分析与蛋白质结合的DNA。基于图谱信息,可以进行差异ChIP,以了解在两个发育阶段定义位点处的顺式调控调节。本章描述了通过同时比较果蝇的两个不同发育阶段来鉴定新靶标的差异ChIP。