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Series GSE106948 Query DataSets for GSE106948
Status Public on Jan 21, 2020
Title Genome wide maps of chromatin modification in response to Hh signaling in mouse embryonic forelimb buds
Organism Mus musculus
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Summary Purpose: The response to Hedgehog signaling in the limb is driven by GLI bound enhancers and the majority of Hh targets in the developing limb bud are regulated solely by the activity of GLI-repressor. Currently we do not have a comprehensive understanding of how GLI bound enhancers respond Hedgehog signaling. The goal of this study is to identify how GLI bound enhancers are regulated by Hedgehog signaling and specifically by GLI-repressor.
Methods: Histone modification ChIP-sequencing was done in Embryonic day 10.5 limb buds from control and Shh null embryos to identify histone modifications that change in response to Hedgehog signaling. We also did a comparative analysis of histone modificaiton response to Hedgehog stimulation in NIH3T3 cells to assess tissue specificity of GLI bound enhancer response to Hedgehog signaling.
Results: We found that Hedgehog signaling specifically regulates the acetylation status of Histone 3 lysine 27 at a subset of GLI binding regions. These regions correlate with both known Hedgehog target genes in the limb bud and with characterized enhancers in the limb. This set of Hedgehog responsive GLI bound enhancers demonstrate enhanced tissue specificity.
 
Overall design ChIP-sequencing of 3 different histone modifications (H3K27ac, H3K4me2, and H3K27me3) in Shh-/- and WT control E10.5 forelimb buds. Additional ChIP-seq of H3K27ac in NIH3T3 cells with and without Hedgehog pathway stimulation. Two biological replicates were done for each ChIP experiment. Enrichment values were determined using input control samples from one or both replicates for each ChIP experiment.
 
Contributor(s) Falkenstein KN, Ji Z, Ji H, Vokes SA
Citation(s) 31989924, 35145123
Submission date Nov 15, 2017
Last update date Mar 09, 2022
Contact name Steven Vokes
E-mail(s) svokes@austin.utexas.edu
Organization name The University of Texas at Austin
Department Department of Molecular Biosciences, Institute for Cellular & Molecular Biology
Street address 2500 Speedway, Stop A4800
City Austin
State/province Texas
ZIP/Postal code 78712
Country USA
 
Platforms (3)
GPL17021 Illumina HiSeq 2500 (Mus musculus)
GPL19057 Illumina NextSeq 500 (Mus musculus)
GPL21103 Illumina HiSeq 4000 (Mus musculus)
Samples (24)
GSM2858040 WT_H3K27ac rep 1
GSM2858041 WT_H3K27ac rep 2
GSM2858042 WT_H3K27ac input
This SubSeries is part of SuperSeries:
GSE108880 GLI transcriptional repression regulates enhancer activity and chromatin accessibility for Hedgehog target genes
Relations
BioProject PRJNA418576
SRA SRP125060

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
GSE106948_H3K27ac_SHHnull_peak.txt.gz 1.8 Mb (ftp)(http) TXT
GSE106948_H3K27ac_WT_peak.txt.gz 2.0 Mb (ftp)(http) TXT
GSE106948_H3K27me3_SHHnull_peak.txt.gz 899.6 Kb (ftp)(http) TXT
GSE106948_H3K4me2_SHHnull_peak.txt.gz 1.6 Mb (ftp)(http) TXT
GSE106948_H3K4me2_WT_peak.txt.gz 1.6 Mb (ftp)(http) TXT
GSE106948_NIH3T3_H3K27ac_control_peak.txt.gz 3.9 Mb (ftp)(http) TXT
GSE106948_NIH3T3_H3K27ac_pur_peak.txt.gz 3.7 Mb (ftp)(http) TXT
GSE106948_RAW.tar 7.0 Gb (http)(custom) TAR (of BEDGRAPH)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file
Processed data are available on Series record

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