BMC Developmental Biology · 2006 · 125 citations · 36 references
Life SciencesBiologyGeneticsEpigenomicsGene ExpressionStem Cell BiologyDevelopmental EpigeneticsDevelopmental EpigenomicsEmbryonic Stem CellsEpigenetic Regulation In DevelopmentGermline Stem CellsReproductive EpigeneticsCpg Island HypomethylationDna Methylation PatternsGermline EpigeneticsMouse Embryonic Stem CellsPromoter HypermethylationSperm EpigeneticsTranscriptional Repression ElementsTranscriptional Repression Mechanisms
BACKGROUND: We previously identified a set of genes called ECATs (ES cell-associated transcripts) that are expressed at high levels in mouse ES cells. Here, we examine the expression and DNA methylation of ECATs in somatic cells and germ cells. RESULTS: In all ECATs examined, the promoter region had low methylation levels in ES cells, but higher levels in somatic cells. In contrast, in spite of their lack of pluripotency, male germline stem (GS) cells expressed most ECATs and exhibited hypomethylation of ECAT promoter regions. We observed a similar hypomethylation of ECAT loci in adult testis and isolated sperm. Some ECATs were even less methylated in male germ cells than in ES cells. However, a few ECATs were not expressed in GS cells, and most of them targets of Oct3/4 and Sox2. The Octamer/Sox regulatory elements were hypermethylated in these genes. In addition, we found that GS cells express little Sox2 protein and low Oct3/4 protein despite abundant expression of their transcripts. CONCLUSION: Our results suggest that DNA hypermethylation and transcriptional repression of a small set of ECATs, together with post-transcriptional repression of Oct3/4 and Sox2, contribute to the loss of pluripotency in male germ cells.
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Establishment in culture of pluripotential cells from mouse embryos
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Functional Expression Cloning of Nanog, a Pluripotency Sustaining Factor in Embryonic Stem Cells
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