Analyses of Promoter , Enhancer, and Nucleosome Organization in Mammalian Cells by MNase-Seq

Methods Mol Biol. 2021:2351:93-104. doi: 10.1007/978-1-0716-1597-3_5.

Abstract

MNase-Seq is a genome-wide procedure that allows mapping of DNA associated to nucleosomes following micrococcal nuclease digestion. It is a rapid and robust technology useful for the analysis of chromatin properties genome-wide at the resolution of mono-nucleosomes. Here, we describe how to produce high-resolution nucleosome maps of cells grown in suspension or adherent mammalian cells. After only three steps: nuclei or cell preparation, native MNase digestion and DNA purification, libraries for high-throughput sequencing can be prepared. Genome-wide nucleosome maps allow analyzing chromatin opening at promoters or enhancers, nucleosome displacement, or labile nucleosome occupancy depending on the digestion condition used. As presented, MNase-Seq is a versatile tool for investigating chromatin dynamics, regulation, and to define open chromatin regions of regulatory elements in mammalian genomes.

Keywords: Chromatin; Enhancer; High-throughput sequencing; MNase-Seq; Nucleosome; Promoter.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cells, Cultured
  • Chromatin / genetics
  • Chromatin / metabolism
  • Chromosome Mapping
  • Computational Biology / methods
  • Enhancer Elements, Genetic*
  • Gene Library
  • Genome-Wide Association Study / methods*
  • High-Throughput Nucleotide Sequencing / methods*
  • Nucleosomes / metabolism*
  • Promoter Regions, Genetic*

Substances

  • Chromatin
  • Nucleosomes