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Series GSE9172 Query DataSets for GSE9172
Status Public on Jan 28, 2008
Title Mapping Promoter CpG Methylation in mESCs
Organism Mus musculus
Experiment type Expression profiling by array
Methylation profiling by genome tiling array
Summary DNA methylation and histone modifications influence gene activities in a variety of mammalian cells. We report here the large scale mapping of DNA methylation patterns at proximal promoter regions in mouse embryonic stem cells (mESCs). A majority of methylated genes represent cell differentiation-associated genes that are repressed in mESCs. In contrast, unmethylated genes include many housekeeping and pluripotency genes such as STAT3 and Oct4/Nanog/Sox2, which are essential for ESC self-renewal. By comparing methylation patterns to the binding domains of Oct4/Nanog, Polycomb proteins, and histone H3 lysine (K) 4/27 trimethylation on gene promoters, we found that promoter DNA methylation is frequently the only epigenetic marker associated with a subset of silenced genes in mESCs that do not possess H3 K4/K27 trimethylation marks and are free from the binding of Polycomb proteins and the Oct4/Nanog transcription factors. Gene expression profiling of demethylated mESCs showed that a majority of up-regulated genes, including a subset of X-linked genes and many development genes, represent a distinct population of genes that are neither targeted by Polycomb and Oct4/Nanog, nor carry H3 K4/K27 trimethylation marks. Our data suggest that promoter methylation patterns in mESCs represent a unique epigenetic program that complements other regulatory mechanisms to allow the expression of pluripotency genes, but represses a subset of genes that will only be activated in specific cell lineages upon cell differentiation.
Keywords: DNA Methylation, methylated DNA immunoprecipitation
 
Overall design We compared DNA methylation patterns in Wildtype (J1) and DNA methylation deficient (TKO) mouse ES cells. We performed 7 replicates using different passages of mouse ES cells. For gene expression analysis, we used the same cultures and performed 3 replicates. The supplied table is the average log ratio for the 3 replicates and takes into account the dye swap of replicate 2.
 
Contributor(s) Fouse SD, Shen Y, Pellegrini M, Cole S, Meissner A, Van Neste L, Jaenisch R, Fan G
Citation(s) 18371437
Submission date Sep 26, 2007
Last update date Jan 18, 2013
Contact name Yin Shen
E-mail(s) yshen@mednet.ucla.edu
Organization name UCLA
Street address 695 Charles E. Young Dr.
City Los Angeles
State/province CA
ZIP/Postal code 90095
Country USA
 
Platforms (3)
GPL2872 Agilent-012694 Whole Mouse Genome G4122A (Feature Number version)
GPL5805 Agilent-013276 Mouse Promoter ChIP-on-Chip Set 44k, Microarray 2 of 2
GPL5806 Agilent-013275 Mouse Promoter ChIP-on-Chip Set 44k, Microarray 1 of 2
Samples (15)
GSM227260 Promoter CpG Methylation in Mouse ES cells (1/2) replicate 1
GSM227261 Promoter CpG Methylation in Mouse ES Cells (1/2) replicate 2
GSM227262 Promoter CpG Methylation in Mouse ES Cells (1/2) replicate 4
Relations
BioProject PRJNA102733

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
GSE9172_RAW.tar 191.1 Mb (http)(custom) TAR (of TXT)
Processed data included within Sample table

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