Genome-wide in vitro reconstitution of yeast chromatin with in vivo-like nucleosome positioning.

Nils Krietenstein, Christian J Wippo, Corinna Lieleg, Philipp Korber
Author Information
  1. Nils Krietenstein: Adolf-Butenandt-Institut, Molecular Biology Unit, University of Munich, Munich, Germany.

Abstract

Recent genome-wide mapping of nucleosome positions revealed that well-positioned nucleosomes are pervasive across eukaryotic genomes, especially in important regulatory regions such as promoters or origins of replication. As nucleosomes impede access to DNA, their positioning is a primary mode of genome regulation. In vivo studies, especially in yeast, shed some light on factors involved in nucleosome positioning, but there is an urgent need for a complementary biochemical approach in order to confirm their direct roles, identify missing factors, and study their mechanisms. Here we describe a method that allows the genome-wide in vitro reconstitution of nucleosomes with very in vivo-like positions by a combination of salt gradient dialysis reconstitution, yeast whole cell extracts, and ATP. This system provides a starting point and positive control for the biochemical dissection of nucleosome positioning mechanisms.

MeSH Term

Adenosine Triphosphate
Animals
Chromatin
Chromatin Assembly and Disassembly
DNA Restriction Enzymes
DNA, Fungal
Dialysis
Drosophila
Electrophoresis, Polyacrylamide Gel
Electroporation
Escherichia coli
Genome, Fungal
Genomic Library
Histones
Micrococcal Nuclease
Nucleic Acid Conformation
Nucleosomes
Plasmids
Saccharomyces cerevisiae
Sodium Chloride
Titrimetry

Chemicals

Chromatin
DNA, Fungal
Histones
Nucleosomes
Sodium Chloride
Adenosine Triphosphate
DNA Restriction Enzymes
Micrococcal Nuclease

Word Cloud

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