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Status |
Public on May 01, 2024 |
Title |
U2OS, pLVX-NAB2-STAT6, control, EGR1, biol rep1 |
Sample type |
SRA |
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Source name |
U2OS
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Organism |
Homo sapiens |
Characteristics |
cell line: U2OS cell type: osteosarcoma genotype: pLVX-NAB2-STAT6 treatment: No treatment chip antibody: EGR1 (Bethyl A303-390A)
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Treatment protocol |
Lentiviruses were produced in HEK293T cells by co-transfection 8 ug of pLVX-Tet-On Advanced (ClonTech) and pLVX-NAB2-STAT6-FLAG-Tight-Puro. U2OS were passaged into a 6-well plate at 30-40 % confluence. When the cells reached 60-70% confluence, 2 ml of virus medium per well (cell medium with 4 ul of lentiviral particles per ml and 8 ug/ml polybrene (Thermo Fisher, cat#TR1003G)) was added to replace old medium. 24 hours after induction, the virus medium was removed and replaced with fresh cell culture medium for another 48 hours. After that, cells were selected with 200 ug/ml of Neomycin (Corning, cat#MT30234CR) in fresh medium. Cells were selected in Neomycin for two weeks with fresh media being added 3-4 weeks and cells split 1:3 when reaching 80-90% confluency. Then cells were plated into a 6-well plate at 30-40 % confluence. When the cells reached 60-70% confluence, 2 ml of medium fresh lentivirus media generated using pLVX-NAB2-STAT6-FLAG-Tight-Puro with 8 ug/ml polybrene (Thermo Fisher, cat#TR1003G) per well was added to replace the old medium. 24 hours after induction, the virus medium was removed and replaced with fresh cell culture medium for another 48 hours. After that, cells were selected with 0.5 ug/ml of puromycin in fresh medium (InvivoGen, cat#ant-pr-1). 48 hours after selection with puromycin, cells were disassociated with Trypsin and plated at a low density in a 15 cm dish. Single cells were cultured with 0.5 ug/ml of puromycin for the next 2-3 weeks until colonies appeared. Individual microcolonies were moved to a 96-well plate for clonal expansion. Clones were screened after addition of 1ug/mL Doxycline by verified by Western Blot. ChIP-seq was done without doxycycline treatment and after 2 days of 1ug/mL doxycycline treatment.
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Growth protocol |
U2OS cells were cultured and maintained in Dulbecco's Modified Eagle's Medium (DMEM) supplemented with 10% super calf serum and Glutmax.
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Extracted molecule |
genomic DNA |
Extraction protocol |
Lysates were clarified from sonicated nuclei (Covaris S220), and protein-DNA complexes were isolated with antibody-conjugated Dynabeads NEBNext Ultra II DNA Library Prep Kit for Illumina (New England Biolabs Inc.)
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Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
NextSeq 2000 |
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Description |
EGR1 ChIP-seq in U2OS pLVX-NAB2-STAT6 cells in control conditions
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Data processing |
Image analysis: Firecrest (Illumina pipeline 1.9, default parameters) Base calling: Bustard (Illumina pipeline 1.9, default parameters) Quality control: FastQC Adapter trimming: Trim Galore! Alignment (ChIPseq): BWA-MEM Tag density files: deepTools bamCoverage Genome_build: GRCh37/hg19 Assembly: hg19 Supplementary files format and content: Supplementary_files_format_and_content: strand-specific bigWig, compatible with UCSC Genome Browser, generated using the deepTools package (bamCoverage function, with RPGC [reads per genome coverage] normalization)
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Submission date |
Dec 08, 2023 |
Last update date |
May 01, 2024 |
Contact name |
Alessandro Gardini |
E-mail(s) |
agardini@wistar.org
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Phone |
2158983755
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Organization name |
The Wistar Institute
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Lab |
Gardini Lab
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Street address |
3601 Spruce St, Room 230
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City |
Philadelphia |
State/province |
PA |
ZIP/Postal code |
19104 |
Country |
USA |
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Platform ID |
GPL30173 |
Series (2) |
GSE249701 |
NAB2-STAT6 drives an EGR1-dependent neuroendocrine program in Solitary Fibrous Tumors (ChIP-Seq) |
GSE249703 |
NAB2-STAT6 drives an EGR1-dependent neuroendocrine program in Solitary Fibrous Tumors |
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Relations |
BioSample |
SAMN38728131 |
SRA |
SRX22828712 |
Supplementary file |
Size |
Download |
File type/resource |
GSM7959244_U2OS-pLVX-NAB2-STAT6-control-EGR1-ChIP-rep1_mem_srt_q10_rmdup_normalized.bw |
153.2 Mb |
(ftp)(http) |
BW |
SRA Run Selector |
Raw data are available in SRA |
Processed data provided as supplementary file |
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