NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Series GSE48159 Query DataSets for GSE48159
Status Public on Jun 21, 2013
Title Mapping ERβ genomic binding sites reveals unique genomic features and identifies EBF1 as an ERβ interactor [Gro-Seq]
Organism Homo sapiens
Experiment type Expression profiling by high throughput sequencing
Summary The C4-12/Flag.ERβ cell line which stably expressed Flag.ERβ is used to study ERβ genomic functions without ERα interference. Mapping ERβ binding sites in these cells reveals ERβ unique distribution and motif enrichment patterns. Accompanying our mapping results, nascent RNA profiling is performed on cells at the same treatment time. The combined results allow the identification of ERβ target genes. Gene ontology analysis reveals that ERβ targets are enriched in differentiation, development and apoptosis. Concurrently, E2 treatment suppresses proliferation in these cells. Within ERβ binding sites, while the most prevalent binding motif is the canonical ERE, motifs of known ER interactors are also enriched in ERβ binding sites. Moreover, among enriched binding motifs are those of GFI, REST and EBF1, which are unique to ERβ binding sites in these cells. Further characterization confirms the association between EBF1 and the estrogen receptors, which favors the N-terminal region of the receptor. Furthermore, EBF1 negatively regulates ERs at the protein level. In summary, by studying ERβ genomic functions in our cell model, we confirm the anti-proliferative role of ERβ and discover the novel cross talk of ERβ with EBF1 which has various implications in normal physiology.
 
Overall design C4-12/Flag.ERβ cells were treated with 10nM E2 (or ethanol as vehicle control) for 1 hour. Nuclei were extracted and processed with run-on assay. The resultant run-on RNA was reverse-transcribed to generate cDNA library which was subsequently sequenced by Illumina Genome Analyzer II or HiSeq2000. Two samples for each treatment were included in this experiment.
 
Contributor(s) Le TP, Sun M, Luo X, Kraus WL, Greene GL
Citation missing Has this study been published? Please login to update or notify GEO.
Submission date Jun 20, 2013
Last update date May 15, 2019
Contact name Thien Le
E-mail(s) lethien@uchicago.edu
Organization name University of Chicago
Lab Geoffrey Greene
Street address 929 E 57th St W325D
City Chicago
State/province IL
ZIP/Postal code 60637
Country USA
 
Platforms (2)
GPL9115 Illumina Genome Analyzer II (Homo sapiens)
GPL11154 Illumina HiSeq 2000 (Homo sapiens)
Samples (4)
GSM1171524 Veh_1
GSM1171525 Veh_2
GSM1171526 E2_1
This SubSeries is part of SuperSeries:
GSE48161 Mapping ERβ genomic binding sites reveals unique genomic features and identifies EBF1 as an ERβ interactor
Relations
BioProject PRJNA209071
SRA SRP026204

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE48159_GROseq_Downregulated_genes.xlsx.gz 75.2 Kb (ftp)(http) XLSX
GSE48159_GROseq_Upregulated_genes.xlsx.gz 107.2 Kb (ftp)(http) XLSX
GSE48159_RAW.tar 2.0 Mb (http)(custom) TAR (of TXT)
SRA Run SelectorHelp
Processed data are available on Series record
Processed data provided as supplementary file
Raw data are available in SRA

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap