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Series GSE41100 Query DataSets for GSE41100
Status Public on Nov 26, 2012
Title Genome-wide TNFα-induced p65 binding before and after telomerase inhibition in HeLa cells
Organism Homo sapiens
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Summary Chromatin immunoprecipitation sequencing (ChIP-seq) was performed to analyze the effect of telomerase inhibition on TNFα-induced genome-wide p65 binding in HeLa cells. By obtaining over 40 million uniquely mappable reads per sample from ChIP-seq, maps for TNFα-induced p65 binding in absence and presence of an hTERT inhibitor, MST-312, were generated. As expected, TNFα treatment significantly increased genome-wide p65 occupancy. Interestingly, when cells were treated with MST-312 prior to TNFα stimulation, the number of p65 binding sites was reduced. In addition, some binding sites, including important p65 targets like IL6 and TNF, showed a reduced p65 occupancy with a minimum fold change of 1.5, after MST-312 exposure. Taken together, our ChIP-seq data indicate that telomerase is required for optimal p65 binding at a small proportion of p65 target sites upon inflammatory stimuli.
 
Overall design Examination of p65 binding in HeLa cells in absence and presence of TNFα and MST-312.
 
Contributor(s) Saginc G, Zhang Z, Li G, Ghosh A, Leow SC, Liu ET, Tergaonkar V
Citation(s) 23159929
Submission date Sep 24, 2012
Last update date May 15, 2019
Contact name Gaye Saginc
E-mail(s) gayesaginc@gmail.com
Organization name A*STAR
Department Genome Institute of Singapore
Lab Cancer Biology
Street address 60 Biopolis Street
City Singapore
ZIP/Postal code 138672
Country Singapore
 
Platforms (1)
GPL13393 AB SOLiD 4 System (Homo sapiens)
Samples (4)
GSM1008530 DMSOtreated_p65_ChIPSeq
GSM1008531 TNFtreated_p65_ChIPSeq
GSM1008532 TNF-MSTtreated_p65_ChIP-seq
Relations
BioProject PRJNA175811
SRA SRP015860

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Supplementary file Size Download File type/resource
GSE41100_RAW.tar 686.1 Mb (http)(custom) TAR (of BED)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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