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Series GSE38557 Query DataSets for GSE38557
Status Public on Jul 15, 2012
Title DNA methylation dynamics during in vivo differentiation of blood and skin stem cells
Organism Mus musculus
Experiment type Expression profiling by array
Third-party reanalysis
Summary DNA methylation is a mechanism of epigenetic regulation that is common to all vertebrates. Functional studies support its relevance for tissue homeostasis, but the global dynamics of DNA methylation during in vivo differentiation have not been worked out in detail. Here we report high-resolution DNA methylation maps of adult stem cell differentiation in mouse, focusing on 19 purified cell populations of the blood and skin lineages. Except for global demethylation in erythrocytes, observed DNA methylation changes were locus-specific and relatively modest in size. They frequently overlapped with lineage-associated transcription factors and their binding sites, suggesting that DNA methylation may protect cells from aberrant transcription factor activation. DNA methylation and gene expression provided highly complementary information, and combining the two enabled us to infer the blood lineage hierarchy directly from genomic data. In summary, our dataset and analysis demonstrate that in vivo differentiation of adult stem cells is associated with small but informative changes in the distribution of DNA methylation across the mouse genome.
 
Overall design We used microarray data to compare the gene expression profiles between various purified cell populations of the blood and skin lineages. Microarray data were obtained for 13 blood cell types (HSC, MPP1, MPP2, CLP, CMP, MEP, GMP, CD4, CD8, B-cell, Eryth, Granu, Mono) and 6 skin cell types (TBSC, ABSC, MTAC, CLDC, EPro, EDif). A subset of these microarray profiles have already been uploaded to GEO as part of previous research and were reused for the current study (GSE20244: MPP1, MPP2, CLP, CMP, GMP; GSE6506: CD4, CD8, B-cell, Eryth, Granu, Mono; GSE31028: TBSC, ABSC, MTAC). All microarray profiles that had not been made public previously are included here (HSC, MEP, CLDC, EPro, EDif). Furthermore, all data are available for download from the paper's supplementary website (http://invivomethylation.computational-epigenetics.org/).

This submission includes the gene expression component of the study.

The complete dataset representing the GSE38557 Samples, and the GSE20244, GSE6506, and GSE31028 Samples listed above, is linked below as a supplementary file.
 
Contributor(s) Bock C, Beerman I, Lien WH, Rossi DJ, Meissner A
Citation(s) 22841485
Submission date Jun 07, 2012
Last update date Feb 11, 2019
Contact name Christoph Bock
E-mail(s) cbock@cemm.oeaw.ac.at
Organization name CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences
Street address Lazarettgasse 14
City Vienna
ZIP/Postal code 1090
Country Austria
 
Platforms (1)
GPL1261 [Mouse430_2] Affymetrix Mouse Genome 430 2.0 Array
Samples (10)
GSM945546 Hematopoietic stem cell, biological replicate 1
GSM945547 Hematopoietic stem cell, biological replicate 2
GSM945548 Megakaryocyte-erythroid progenitor, biological replicate 1
Relations
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Reanalysis of GSM768827
Reanalysis of GSM768828
Reanalysis of GSM768829
Reanalysis of GSM768830
Reanalysis of GSM768831
BioProject PRJNA168152

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
GSE38557_RAW.tar 33.6 Mb (http)(custom) TAR (of CEL)
GSE38557_complete_dataset.txt.gz 5.8 Mb (ftp)(http) TXT
Processed data included within Sample table
Processed data are available on Series record

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