Literature DB >> 28842899

Whole Genome Chromatin IP-Sequencing (ChIP-Seq) in Skeletal Muscle Cells.

Karl Kamhei So1,2, Xianlu Laura Peng1,2, Hao Sun1,2, Huating Wang3,4.   

Abstract

Transcriptional control of gene expression in skeletal muscle cell is involved in different processes ranging from muscle formation to regeneration. The identification of an increasing number of transcription factors, co-factors, and histone modifications has been greatly advanced by methods that allow studies of genome-wide chromatin-protein interactions. Chromatin immunoprecipitation with massively parallel DNA sequencing, or ChIP-seq, is a powerful tool for identifying binding sites of TFs/co-factors and histone modifications. The major steps of this technique involve immunoprecipitation of fragmented chromatin, followed by high-throughput sequencing to identify the protein bound regions genome-wide. Here, in this protocol, we will illustrate how the entire ChIP-seq is performed using global H3K27ac profiling in myoblast cells as an example.

Keywords:  ChIP-seq; Muscle cells; Transcription

Mesh:

Substances:

Year:  2017        PMID: 28842899     DOI: 10.1007/978-1-4939-7283-8_2

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


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