Genome-wide analyses define different classes of PPARbetadelta target genes characterized by distinct modes of transcriptional regulation (Sequencing)
Sample information curated by ChIP-Atlas
Antigen
Antigen Class
Unclassified
Antigen
Unclassified
Cell type
Cell type Class
Prostate
Cell type
WPMY-1
Primary Tissue
Prostate
Tissue Diagnosis
Normal
Attributes by original data submitter
Sample
Alias
E-MTAB-371:WPMY1 cell culture 1
BioSourceProvider
ATCC
Broker name
ArrayExpress
CellLine
WPMY1
CellType
myofibroblast stromal cell
Description
Protocols: Cells were obtained from the ATCC and cultured in DMEM plus 10% fetal bovine serum. Cells were exposed for 6h to the agonist GW501516 (300nM) or DMSO solvent control, after which they were harvested. DMSO was added in a ratio of 1:10000 of the total media volume - in this case, 2 microliter. After stimulation, the cells were fixed by addition of 37% formaldehyde to a final concentration of 1%. Incubation time was 10 min at room temperature. Glycine was added to a final concentration of 125 mM for 5 min. After two washes with ice-cold phosphate-buffered saline, the cells were pelleted for 5 min at 1200 g. Pellets were resuspended in cold hypotonic lysis buffer [5 mM PIPES, pH 8.0, 85 mM KCl, 0.5% (v/v) NP40, and protease inhibitor cocktail (Sigma)] at a ratio of 1 ml per 10^7 cells and incubated on ice for 20 min. Nuclei were pelleted by centrifugation as before and resuspended in radioimmunoprecipitation assay buffer [10 mM Tris-HCl, pH 7.4, 150 mM NaCl, 1% (v/v) NP40, 1% sodium deoxycholate, 0.1% (w/v) SDS, 1 mM EDTA, and protease inhibitors] at a ratio of 1 ml per 10^7 nuclei. Soluble chromatin was prepared by sonication with a microtip using a sonifier (S-250D; Branson Ultrasonics Corporation, Danbury, CT) set to 1-s pulse, 2-s pause. Sixty pulses were applied. After centrifugation at 16,000g for 15 min in a tabletop centrifuge, the supernatant was collected. An aliquot was incubated overnight with proteinase K and RNase A at 65C and loaded on a 1% agarose gel to estimate shearing efficiency. The supernatant was precleared by addition of protein A Sepharose beads (Invitrogen), which were previously blocked in radioimmuno-precipitation assay buffer with 1 mg/ml bovine serum albumin, 0.4 mg/ml sonicated salmon sperm DNA (Stratagene), and protease inhibitors, coupled to rabbit IgG (Sigma I5006). After rotation for 1 h at 4C, the beads were removed by centrifugation. The supernatant was used for immunpreciptiations. Four micrograms of antibody were added to 300ul of precleared chromatin corresponding to 3 x 10^6 nuclei and incubated overnight at 4C with mild rotation. After addition of blocked Sepharose beads, incubation time was 1 h at 4C with mild rotation. The beads were washed once with 1 ml of chilled mixed micelle buffer [20 mM Tris, pH 8.1, 150 mM NaCl, 2 mM EDTA, 0.1% (w/v) SDS, and 1% (v/v) Triton X-100], once with buffer 500 [20 mM Tris, pH 8.1, 500 mM NaCl, 2 mM EDTA, 0.1% (w/v) SDS, and 1% (v/v) Triton X-100], twice with LiCl detergent buffer (10 mM Tris, pH 8.1, 250 mM LiCl, 1% (v/v) NP40, 1% (w/v) sodium deoxycholate, and 1 mM EDTA), and twice with room-temperature Tris-EDTA. Complexes were eluted twice with 25ul of elution buffer [1% SDS (w/v) and 100 mM NaHCO3]. Supernatants were pooled; adjusted to 180 mM NaCl, 35 mM Tris, pH 6.5, and 9 mM EDTA; and incubated with 20 microgram of proteinase K and 1ug of RNase A for 65C overnight. DNA was purified using a PCR purification kit (Qiagen, Hilden, Germany).
INSDC center alias
HELMHOLTZ CENTRE FOR
INSDC center name
HELMHOLTZ CENTRE FOR
INSDC first public
2010-12-31T00:00:09Z
INSDC last update
2018-03-08T15:25:09Z
INSDC status
public
SRA accession
ERS014502
Sample Name
ERS014502
Title
WPMY1 cell culture 1
Sequenced DNA Library
library_name
PPAR DMSO 100308 extract
library_strategy
ChIP-Seq
library_source
GENOMIC
library_selection
ChIP
library_construction_protocol
Cells were obtained from the ATCC and cultured in DMEM plus 10% fetal bovine serum. Cells were exposed for 6h to the agonist GW501516 (300nM) or DMSO solvent control, after which they were harvested. DMSO was added in a ratio of 1:10000 of the total media volume - in this case, 2 microliter. After stimulation, the cells were fixed by addition of 37% formaldehyde to a final concentration of 1%. Incubation time was 10 min at room temperature. Glycine was added to a final concentration of 125 mM for 5 min. After two washes with ice-cold phosphate-buffered saline, the cells were pelleted for 5 min at 1200 g. Pellets were resuspended in cold hypotonic lysis buffer [5 mM PIPES, pH 8.0, 85 mM KCl, 0.5% (v/v) NP40, and protease inhibitor cocktail (Sigma)] at a ratio of 1 ml per 10^7 cells and incubated on ice for 20 min. Nuclei were pelleted by centrifugation as before and resuspended in radioimmunoprecipitation assay buffer [10 mM Tris-HCl, pH 7.4, 150 mM NaCl, 1% (v/v) NP40, 1% sodium deoxycholate, 0.1% (w/v) SDS, 1 mM EDTA, and protease inhibitors] at a ratio of 1 ml per 10^7 nuclei. Soluble chromatin was prepared by sonication with a microtip using a sonifier (S-250D; Branson Ultrasonics Corporation, Danbury, CT) set to 1-s pulse, 2-s pause. Sixty pulses were applied. After centrifugation at 16,000g for 15 min in a tabletop centrifuge, the supernatant was collected. An aliquot was incubated overnight with proteinase K and RNase A at 65C and loaded on a 1% agarose gel to estimate shearing efficiency. The supernatant was precleared by addition of protein A Sepharose beads (Invitrogen), which were previously blocked in radioimmuno-precipitation assay buffer with 1 mg/ml bovine serum albumin, 0.4 mg/ml sonicated salmon sperm DNA (Stratagene), and protease inhibitors, coupled to rabbit IgG (Sigma I5006). After rotation for 1 h at 4C, the beads were removed by centrifugation. The supernatant was used for immunpreciptiations. Four micrograms of antibody were added to 300ul of precleared chromatin corresponding to 3 x 10^6 nuclei and incubated overnight at 4C with mild rotation. After addition of blocked Sepharose beads, incubation time was 1 h at 4C with mild rotation. The beads were washed once with 1 ml of chilled mixed micelle buffer [20 mM Tris, pH 8.1, 150 mM NaCl, 2 mM EDTA, 0.1% (w/v) SDS, and 1% (v/v) Triton X-100], once with buffer 500 [20 mM Tris, pH 8.1, 500 mM NaCl, 2 mM EDTA, 0.1% (w/v) SDS, and 1% (v/v) Triton X-100], twice with LiCl detergent buffer (10 mM Tris, pH 8.1, 250 mM LiCl, 1% (v/v) NP40, 1% (w/v) sodium deoxycholate, and 1 mM EDTA), and twice with room-temperature Tris-EDTA. Complexes were eluted twice with 25ul of elution buffer [1% SDS (w/v) and 100 mM NaHCO3]. Supernatants were pooled; adjusted to 180 mM NaCl, 35 mM Tris, pH 6.5, and 9 mM EDTA; and incubated with 20 microgram of proteinase K and 1ug of RNase A for 65C overnight. DNA was purified using a PCR purification kit (Qiagen, Hilden, Germany).