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Series GSE25688 Query DataSets for GSE25688
Status Public on May 23, 2011
Title Cell Type-Specific DNA Methylation at Intragenic CpG Islands in the Immune System (MAP-Seq and ChIP-Seq data)
Organism Mus musculus
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Methylation profiling by high throughput sequencing
Summary Human and mouse genomes contain a similar number of CpG islands (CGIs), which are discrete CpG-rich DNA sequences associated with transcription start sites. In both species, about 50% of all CGIs are remote from annotated promoters, but nevertheless often have promoter-like features. To document the role of CGI methylation in cell differentiation, we analysed DNA methylation at a comprehensive CGI set in cells of the mouse hematopoietic lineage. Using a method that potentially detects ~33% of genomic CpGs in the methylated state (>7 million) we found that large differences in gene expression were accompanied by surprisingly few DNA methylation changes. There were, however, many DNA methylation differences between hematopoietic cells and a distantly related tissue, brain. Altered DNA methylation occurred predominantly at CGIs within gene bodies, which have the properties of cell type-restricted promoters, but infrequently at annotated gene promoters or CGI flanking sequences. Elevated intragenic CGI methylation correlated with silencing of the associated gene. Differentially methylated intragenic CGIs tended to lack H3K4me3 and associate with a transcriptionally repressive environment regardless of methylation state. Our results indicate that DNA methylation changes play a relatively minor role in the late stages of differentiation, but point to a distinct role for intragenic CGIs.
 
Overall design Mouse immune cells (dendritic cells, B cells, CD4 T cells, Th1 and Th2 cells) were isolated and DNA methylation and gene expression profiled. Methylation and expression patterns were compared to those in brain. DNA methylation was profiled using MAP-seq and two replicates were carried out for each cell type of interest.
 
Contributor(s) Deaton AM, Webb S, Kerr AR, Illingworth RS, Guy J, Andrews R, Bird A
Citation(s) 21628449
Submission date Nov 29, 2010
Last update date May 15, 2019
Contact name Adrian Bird
E-mail(s) a.bird@ed.ac.uk
Phone 0131 6508695
Fax 0131 6505379
Organization name The University of Edinburgh
Department WTCCB
Street address Mayfield Road
City Edinburgh
ZIP/Postal code EH9 3JR
Country United Kingdom
 
Platforms (1)
GPL9185 Illumina Genome Analyzer (Mus musculus)
Samples (10)
GSM630887 DC_MAP
GSM630888 Bcell_MAP
GSM630889 CD4_1_MAP
This SubSeries is part of SuperSeries:
GSE25689 Cell Type-Specific DNA Methylation at Intragenic CpG Islands in the Immune System
Relations
BioProject PRJNA142449
SRA SRP004771

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
GSE25688_RAW.tar 2.5 Gb (http)(custom) TAR (of BEDGRAPH)
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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