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Sample GSM7959244 Query DataSets for GSM7959244
Status Public on May 01, 2024
Title U2OS, pLVX-NAB2-STAT6, control, EGR1, biol rep1
Sample type SRA
 
Source name U2OS
Organism Homo sapiens
Characteristics cell line: U2OS
cell type: osteosarcoma
genotype: pLVX-NAB2-STAT6
treatment: No treatment
chip antibody: EGR1 (Bethyl A303-390A)
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.
Growth protocol U2OS cells were cultured and maintained in Dulbecco's Modified Eagle's Medium (DMEM) supplemented with 10% super calf serum and Glutmax.
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.)
 
Library strategy ChIP-Seq
Library source genomic
Library selection ChIP
Instrument model NextSeq 2000
 
Description EGR1 ChIP-seq in U2OS pLVX-NAB2-STAT6 cells in control conditions
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)
 
Submission date Dec 08, 2023
Last update date May 01, 2024
Contact name Alessandro Gardini
E-mail(s) agardini@wistar.org
Phone 2158983755
Organization name The Wistar Institute
Lab Gardini Lab
Street address 3601 Spruce St, Room 230
City Philadelphia
State/province PA
ZIP/Postal code 19104
Country USA
 
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
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 SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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