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Series GSE53133 Query DataSets for GSE53133
Status Public on May 06, 2015
Title Composite macroH2A/NRF-1 Nucleosomes Suppress Noise and Generate Robustness in Gene Expression
Organism Homo sapiens
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Expression profiling by high throughput sequencing
Summary The histone variant macroH2A has been implicated in transcriptional repression, but the molecular mechanisms that contribute to global macroH2A-dependent genome regulation remain elusive. Using ChIP-seq coupled with transcriptional profiling in macroH2A knock-down cells (GSE53103) we demonstrate that singular macroH2A nucleosomes occupy transcription start sites of subsets of both expressed and repressed genes with opposing regulatory consequences. Specifically macroH2A nucleosomes mask repressor binding sites in expressed genes, but activator binding sites in repressed genes thus generating distinct chromatin landscapes limiting genetic or extracellular inductive signals. We show that composite nucleosomes containing macroH2A and NRF-1 are stably positioned on gene regulatory regions and can buffer the transcriptional noise typifying antiviral responses. In contrast, macroH2A nucleosomes without NRF-1 bind promoters weakly and mark genes with noisier gene expression patterns. Thus, the strategic position and stabilization of macroH2A nucleosomes in human promoters defines robust gene expression patterns.
 
Overall design ChIP-seq experiments were performed in human Namalwa B cells and Hela epithelial cells in order to investigate the function of specialized nucleosomes containing the macroH2A histone variant and the transcription factor NRF-1. Native ChIP, Native RecHIP or crosslink ChIP were performed in replicates, sequenced and aligned to the reference genome (hg18).
mRNA-seq experiments were performed in human Namalwa B cells using a strand-specific protocol.
Please see manuscript for details.
 
Contributor(s) Lavigne MD, Thanos D
Citation(s) 25959814
Submission date Dec 09, 2013
Last update date May 15, 2019
Contact name Dimitris Thanos
E-mail(s) thanos@bioacademy.gr
Organization name BIOMEDICAL RESEARCH FOUNDATION ACADEMY OF ATHENS (BRFAA)
Department Basic Research II
Lab Molecular Biology
Street address 4 Soranou Ephessiou
City Athens
ZIP/Postal code 115 27
Country Greece
 
Platforms (3)
GPL9115 Illumina Genome Analyzer II (Homo sapiens)
GPL10999 Illumina Genome Analyzer IIx (Homo sapiens)
GPL11154 Illumina HiSeq 2000 (Homo sapiens)
Samples (10)
GSM1282845 Namalwa_anti-mH2A1_replicate1
GSM1282846 Namalwa_anti-mH2A1_replicate2
GSM1282847 Namalwa_Input_Replicate1
Relations
BioProject PRJNA230966
SRA SRP033612

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
GSE53133_HeLa_Input_Replicate1+2.bed.gz 77.7 Mb (ftp)(http) BED
GSE53133_HeLa_anti-mH2A1_replicate1+2.bed.gz 210.6 Mb (ftp)(http) BED
GSE53133_Namalwa_Input_Replicate1+2.bed.gz 79.7 Mb (ftp)(http) BED
GSE53133_Namalwa_RNA-seq_RPKM.txt.gz 194.4 Kb (ftp)(http) TXT
GSE53133_Namalwa_anti-NRF1_replicate1+2.bed.gz 66.7 Mb (ftp)(http) BED
GSE53133_Namalwa_anti-mH2A1+NRF1_replicate1+2.bed.gz 1.5 Mb (ftp)(http) BED
GSE53133_Namalwa_anti-mH2A1_replicate1+2.bed.gz 122.0 Mb (ftp)(http) BED
GSE53133_RAW.tar 244.4 Mb (http)(custom) TAR (of TXT)
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Raw data are available in SRA
Processed data are available on Series record

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