Profiling Accessible Chromatin and Nucleosomes in the Mammalian Genome
- PMID: 36427143
- DOI: 10.1007/978-1-0716-2847-8_6
Profiling Accessible Chromatin and Nucleosomes in the Mammalian Genome
Abstract
Genomic DNA wraps around core histones to form nucleosomes, which provides steric constraints on how transcription factors (TFs) can interact with gene regulatory sequences. It is increasingly apparent that well-positioned, accessible nucleosomes are an inherent feature of active enhancers and can facilitate cooperative TF binding, referred to as nucleosome-mediated cooperativity. Thus, profiling chromatin and nucleosome properties (accessibility, positioning, and occupancy) on the genome is crucial to understand cell-type-specific gene regulation. Here we describe a simplified protocol to profile accessible nucleosomes in the mammalian genome using low-level and high-level micrococcal nuclease (MNase) digestion followed by genome-wide sequencing.
Keywords: Accessible nucleosome; Chromatin accessibility; Fragile nucleosome; MNase-seq; Nucleosome occupancy; Nucleosome positioning.
© 2023. The Author(s), under exclusive license to Springer Science+Business Media, LLC, part of Springer Nature.
References
-
- Rao S, Ahmad K, Ramachandran S (2021) Cooperative binding between distant transcription factors is a hallmark of active enhancers. Mol cell 81:1651–1665.e4. https://doi.org/10.1016/j.molcel.2021.02.014 - DOI - PubMed
-
- Sönmezer C, Kleinendorst R, Imanci D, Barzaghi G, Villacorta L, Schübeler D, Benes V, Molina N, Krebs AR (2021) Molecular co-occupancy identifies transcription factor binding cooperativity in vivo. Mol Cell 81:255–267.e6. https://doi.org/10.1016/j.molcel.2020.11.015 - DOI - PubMed
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Miscellaneous