The Polycomb group protein Eed protects the inactive X-chromosome from differentiation-induced reactivation

The Polycomb group (PcG) encodes an evolutionarily conserved set of chromatin-modifying proteins that are thought to maintain cellular transcriptional memory by stably silencing gene expression 1 . In mouse embryos that are mutated for the PcG protein Eed, X-chromosome inactivation (XCI) is not stab...

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Veröffentlicht in:Nature cell biology 2006-02, Vol.8 (2), p.195-202
Hauptverfasser: Kalantry, Sundeep, Mills, Kyle C., Yee, Della, Otte, Arie P., Panning, Barbara, Magnuson, Terry
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Sprache:eng
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Zusammenfassung:The Polycomb group (PcG) encodes an evolutionarily conserved set of chromatin-modifying proteins that are thought to maintain cellular transcriptional memory by stably silencing gene expression 1 . In mouse embryos that are mutated for the PcG protein Eed, X-chromosome inactivation (XCI) is not stably maintained in extra-embryonic tissues 2 . Eed is a component of a histone-methyltransferase complex that is thought to contribute to stable silencing in undifferentiated cells due to its enrichment on the inactive X-chromosome in cells of the early mouse embryo and in stem cells of the extra-embryonic trophectoderm lineage 3 , 4 , 5 , 6 , 7 , 8 . Here, we demonstrate that the inactive X-chromosome in Eed −/− trophoblast stem cells and in cells of the trophectoderm-derived extra-embryonic ectoderm in Eed −/− embryos remain transcriptionally silent, despite lacking the PcG-mediated histone modifications that normally characterize the facultative heterochromatin of the inactive X-chromosome. Whereas undifferentiated Eed −/− trophoblast stem cells maintained XCI, reactivation of the inactive X-chromosome occurred when these cells were differentiated. These results indicate that PcG complexes are not necessary to maintain transcriptional silencing of the inactive X-chromosome in undifferentiated stem cells. Instead, PcG proteins seem to propagate cellular memory by preventing transcriptional activation of facultative heterochromatin during differentiation.
ISSN:1465-7392
1476-4679
1476-4679
DOI:10.1038/ncb1351