Analysis of nucleosome positioning using a nucleosome-scanning assay.

Juan Jose Infante, G Lynn Law, Elton T Young
Author Information
  1. Juan Jose Infante: Department of Microbiology, University of Washington, Seattle, WA, USA.

Abstract

The nucleosome-scanning assay (NuSA) couples isolation of mononucleosomal DNA after micrococcal nuclease (MNase) digestion with quantitative real-time PCR (qPCR) to map nucleosome positions in chromatin. It is a relatively simple, rapid procedure that can produce a high-resolution map of nucleosome location and occupancy and thus is suitable for analyzing individual promoters in great detail. The analysis can also quantify the protection of DNA sequences due to interaction with proteins other than nucleosomes and show how this protection varies when conditions change. When coupled with chromatin immunoprecipitation (ChIP), NuSA can identify histone variants and modifications associated with specific nucleosomes.

Grants

  1. R01 GM026079/NIGMS NIH HHS
  2. GM26079/NIGMS NIH HHS

MeSH Term

Biological Assay
Chromatin Immunoprecipitation
DNA, Fungal
Micrococcal Nuclease
Nucleosomes
Promoter Regions, Genetic
Proteolysis
Real-Time Polymerase Chain Reaction
Saccharomyces cerevisiae
Saccharomyces cerevisiae Proteins
Spheroplasts
Statistics as Topic

Chemicals

DNA, Fungal
Nucleosomes
Saccharomyces cerevisiae Proteins
Micrococcal Nuclease