Unit

UNIT 21.24 ChIP-exo Method for Identifying Genomic Location of DNA-Binding Proteins with Near-Single-Nucleotide Accuracy

  1. Ho Sung Rhee,
  2. B. Franklin Pugh

Published Online: 1 OCT 2012

DOI: 10.1002/0471142727.mb2124s100

Current Protocols in Molecular Biology

Current Protocols in Molecular Biology

How to Cite

Rhee, H. S. and Pugh, B. F. 2012. ChIP-exo Method for Identifying Genomic Location of DNA-Binding Proteins with Near-Single-Nucleotide Accuracy. Current Protocols in Molecular Biology. 100:21.24:21.24.1–21.24.14.

Author Information

  1. Pennsylvania State University, University Park, Pennsylvania

Publication History

  1. Published Online: 1 OCT 2012
  2. Published Print: OCT 2012

Abstract

This unit describes the ChIP-exo methodology, which combines chromatin immunoprecipitation (ChIP) with lambda exonuclease digestion followed by high-throughput sequencing. ChIP-exo allows identification of a nearly complete set of the binding locations of DNA-binding proteins at near-single-nucleotide resolution with almost no background. The process is initiated by cross-linking DNA and associated proteins. Chromatin is then isolated from nuclei and subjected to sonication. Subsequently, an antibody against the desired protein is used to immunoprecipitate specific DNA-protein complexes. ChIP DNA is purified, sequencing adaptors are ligated, and the adaptor-ligated DNA is then digested by lambda exonuclease, generating 25- to 50-nucleotide fragments for high-throughput sequencing. The sequences of the fragments are mapped back to the reference genome to determine the binding locations. The 5′ ends of DNA fragments on the forward and reverse strands indicate the left and right boundaries of the DNA-protein binding regions, respectively. Curr. Protoc. Mol. Biol. 100:21.24.1-21.24.14. © 2012 by John Wiley & Sons, Inc.

Keywords:

  • ChIP;
  • ChIP-exo;
  • binding location;
  • genome-wide;
  • lambda exonuclease