Calibrating ChIP-Seq with Nucleosomal Internal Standards to Measure Histone Modification Density Genome Wide

Mol Cell. 2015 Jun 4;58(5):886-99. doi: 10.1016/j.molcel.2015.04.022. Epub 2015 May 21.


Chromatin immunoprecipitation (ChIP) serves as a central experimental technique in epigenetics research, yet there are serious drawbacks: it is a relative measurement, which untethered to any external scale obscures fair comparison among experiments; it employs antibody reagents that have differing affinities and specificities for target epitopes that vary in abundance; and it is frequently not reproducible. To address these problems, we developed Internal Standard Calibrated ChIP (ICeChIP), wherein a native chromatin sample is spiked with nucleosomes reconstituted from recombinant and semisynthetic histones on barcoded DNA prior to immunoprecipitation. ICeChIP measures local histone modification densities on a biologically meaningful scale, enabling unbiased trans-experimental comparisons, and reveals unique insight into the nature of bivalent domains. This technology provides in situ assessment of the immunoprecipitation step, accommodating for many experimental pitfalls as well as providing a critical examination of untested assumptions inherent to conventional ChIP.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Calibration
  • Cell Line
  • Chromatin Immunoprecipitation / standards*
  • Drosophila melanogaster
  • Genome
  • HEK293 Cells
  • Histones / metabolism*
  • Humans
  • Methylation
  • Mice
  • Nucleosomes / genetics*
  • Protein Processing, Post-Translational*
  • Reference Standards
  • Reproducibility of Results
  • Sequence Analysis, DNA


  • Histones
  • Nucleosomes

Associated data

  • GEO/GSE60378