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SRX16989212: GSM6437269: Histone H3 MNase ChIP-seq total chromatin replicate 1; Mus musculus; ChIP-Seq
1 ILLUMINA (Illumina HiSeq 4000) run: 39.4M spots, 3G bases, 1.2Gb downloads

External Id: GSM6437269_r1
Submitted by: LEM, CEA
Study: Nucleosomal and subnucleosomal organization of transcription cis-regulatory elements in mouse embryonic stem cells
show Abstracthide Abstract
We report a comprehensive analysis of nucleosomal and subnucleosomal organization at cis-regulatory elements (CREs) in mouse embryonic stem (ES) cells. We used chromatin fragmented by a moderate dose of micrococcal nuclease (MNase) as input for ChIP-seq with antibodies against histones and transcription factors and high-coverage deep-sequencing. Centrifugation of chromatin through sucrose gradients, followed by ChIP-seq, allowed the characterization of different subclasses of subnucleosomal particles having distribution patterns specific to enhancers, gene promoters and CTCF binding sites. We also provide datasets showing that this particular chromatin organization of CREs is conserved in the human melanoma 501Mel cell line. Overall design: We used MNase ChIP-seq to define the distribution of subnucleosomal particles, canonical nucleosomes, and transcription factors enrichment.
Sample: Histone H3 MNase ChIP-seq total chromatin replicate 1
SAMN30201330 • SRS14574972 • All experiments • All runs
Organism: Mus musculus
Library:
Name: GSM6437269
Instrument: Illumina HiSeq 4000
Strategy: ChIP-Seq
Source: GENOMIC
Selection: ChIP
Layout: PAIRED
Construction protocol: Chromatin preparation: ES cells were collected and fixed in D15 culture medium containing 1 % formaldehyde (Sigma) for 10 min at 20°C. We stopped fixation by adding glycine to 125 mM, and the cells were centrifugated and washed three times with PBS. Cells were then permeabilized in Tris-HCl pH 7.5 15 mM, NaCl 15 mM, MgCl2 5 mM, EGTA 0.1 mM, KCl 60 mM, Sucrose 0.3 M, 0.4% IGEPAL CA-630 (I3021, Sigma) during 15 min on ice. We next diluted the cells with two volumes of MNase buffer (Tris-HCl pH 7.5 20 mM, NaCl 20 mM, CaCl2 2 mM, MgCl2 4 mM, KCl 15 mM, 0.1 M sucrose), and chromatin was digested during 10 min at 37 °C with 6 Kunitz units of MNase (New England Biolabs, 200 Kunitz units/µl) per 1 million cells. We stopped MNase digestion by adding a final concentration of 10 mM EDTA. We released chromatin from MNase-treated ES cells by passing the cell suspension 13 times through a 26G syringe. Next, we centrifuged the samples, and the supernatants containing the solubilized chromatin were used directly for ChIP-seq experiments or sucrose gradient centrifugation. DNA libraries were prepared using MicroPlex Library Preparation Kit v2 or v3 (Diagenode)
Runs: 1 run, 39.4M spots, 3G bases, 1.2Gb
Run# of Spots# of BasesSizePublished
SRR2097155239,405,3403G1.2Gb2023-06-13

ID:
23766688

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