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Updated: Nov 4, 2025

Generation of Native Chromatin Immunoprecipitation Sequencing Libraries for Nucleosome Density Analysis
Published on: December 12, 2017
Rapid and inexpensive preparation of genome-wide nucleosome footprints from model and non-model organisms
Laura E McKnight1, Johnathan G Crandall1, Thomas B Bailey1
1Institute of Molecular Biology, University of Oregon, Eugene, OR 97403, USA.
Abstract:
MNase-seq (micrococcal nuclease sequencing) is used to map nucleosome positions in eukaryotic genomes to study the relationship between chromatin structure and DNA-dependent processes. Current protocols require at least two days to isolate nucleosome-protected DNA fragments. We have developed a streamlined protocol for S. cerevisiae and other fungi which takes only three hours. Modified protocols were developed for wild fungi and mammalian cells. This method for rapidly producing sequencing-ready nucleosome footprints from several organisms makes MNase-seq faster and easier, with less chemical waste.

