Unit

UNIT 17.7 Chromatin Immunoprecipitation for Determining the Association of Proteins with Specific Genomic Sequences In Vivo

  1. Oscar Aparicio1,
  2. Joseph V. Geisberg2,
  3. Kevin Struhl2

Published Online: 1 SEP 2004

DOI: 10.1002/0471143030.cb1707s23

Current Protocols in Cell Biology

Current Protocols in Cell Biology

How to Cite

Aparicio, O., Geisberg, J. V. and Struhl, K. 2004. Chromatin Immunoprecipitation for Determining the Association of Proteins with Specific Genomic Sequences In Vivo. Current Protocols in Cell Biology. 23:17.7:17.7.1–17.7.23.

Author Information

  1. 1

    University of Southern California, Los Angeles, California

  2. 2

    Harvard Medical School, Boston, Massachusetts

Publication History

  1. Published Online: 1 SEP 2004
  2. Published Print: JUN 2004

Abstract

Chromatin immunoprecipitation (ChIP) is a powerful and widely applied technique for detecting the association of individual proteins with specific genomic regions in vivo. Live cells are treated with formaldehyde to generate protein-protein and protein- DNA cross-links between molecules in close proximity on the chromatin template in vivo. DNA sequences that cross-link with a given protein are selectively enriched and reversal of the formaldehyde cross-link permits recovery and quantitative analysis of the immunoprecipitated DNA. As formaldehyde inactivates cellular enzymes essentially immediately upon addition to cells, ChIP provides snapshots of protein-protein and protein- DNA interactions at a particular time point, and hence is useful for kinetic analysis of events occurring on chromosomal sequences in vivo. In addition, ChIP can be combined with microarray technology to identify the location of specific proteins on a genome-wide basis. This unit describes the ChIP protocol for Saccharomyces cerevisiae; however, it is also applicable to other organisms.