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SRX8330549: GSM4548046: 23_p5424_IgG_CR; Mus musculus; OTHER
1 ILLUMINA (Illumina HiSeq 2500) run: 10.9M spots, 540.7M bases, 189Mb downloads

Submitted by: NCBI (GEO)
Study: DNA Double-Strand Breaks Induce H2Ax Phosphorylation Domains in a Contact-Dependent Manner
show Abstracthide Abstract
Efficient repair of DNA double-strand breaks (DSBs) requires a coordinated DNA Damage Response (DDR), which includes phosphorylation of histone H2Ax, forming ?H2Ax. This histone modification spreads beyond the DSB into neighboring chromatin, generating a DDR platform that protects against end disassociation and degradation, minimizing chromosomal rearrangements. However, mechanisms that determine the breadth and intensity of ?H2Ax domains remain unclear. Here, we show that chromosomal contacts of a DSB site are the primary determinants for ?H2Ax landscapes. DSBs that disrupt a topological border permit extension of ?H2Ax domains into both adjacent compartments. In contrast, DSBs near a border produce highly asymmetric DDR platforms, with ?H2Ax nearly absent from one broken end. Collectively, our findings lend insights into a basic DNA repair mechanism and how the precise location of a DSB may influence genome integrity. Overall design: Examination of 2 different chromatin modification in 3 cell types Examination of chromatin topology by Hi-C in 3 different types and 3 different conditions
Sample: 23_p5424_IgG_CR
SAMN14897261 • SRS6649956 • All experiments • All runs
Organism: Mus musculus
Library:
Instrument: Illumina HiSeq 2500
Strategy: OTHER
Source: GENOMIC
Selection: other
Layout: SINGLE
Construction protocol: Cells were washed 1X with cut and run wash buffer (20 mM HEPES, pH7.5, 150 mM NaCl, 0.5 mM spermidine), bound to activated ConA beads (Bangs Laboratories BP531), permeabilized in digi buffer (wash buffer + 0.002% digitonin), incubated with antibodies (1 g/CR in digi buffer), washed in digi buffer, incubated with pA-MN (gift from Heinkoff Laboratory, currently EpiCypher 15-1016), and washed in digi buffer. Following the final wash, cells were washed with ice-cold low salt wash buffer (20 mM HEPES, pH 7.5, 0.5 mM spermidine, 0.002% digitonin) and digested using MN-ase digestion buffer (3.5 mM HEPES pH 7.5, 10 mM CaCl2, 0.002% digitonin) for 25 minutes on ice. Solubilized chromatin was released using an isosmotic stop buffer (170 mM NaCl, 20 mM EGTA, 0.05% Digitonin, 20 µg/ml glycogen, 25 µg/ml RNase A, 2 pg/ml S. cerevisiae fragmented nucleosomal DNA) and was collected using a PCR clean up kit column (EZbioresearch M1001). All antibody incubations and digitonin washing steps were performed for 5 minutes at room temperature and included protease, phosphatase and deacetylase inhibitors (Roche). For library preparation, DNA products were incubated with an end repair master mix (1 X T4 ligation buffer, dNTP, ATP, T4 PNK, T4 DNA Pol and TAQ DNA polymerase) and incubated as follows: 12'C 15 minutes (end polishing), 37'C 15 minutes (5' end phosphorylation) and 58'C 1.5 hour (dA tailing). Polished libraries were purified using AmpureXP beads and ligated to either NEBNext Dual Index (NEB) or Illuminia TruSeq adaptors. Libraries were size selected and enriched by PCR. Finished libraries were sequenced using Illumina HiSeq2500 (Genome Technology Access Center, Washington University).
Experiment attributes:
GEO Accession: GSM4548046
Links:
Runs: 1 run, 10.9M spots, 540.7M bases, 189Mb
Run# of Spots# of BasesSizePublished
SRR1177768210,923,172540.7M189Mb2020-05-19

ID:
10836452

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