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Previous studies have implicated the Eed-Enx1 Polycomb group complex in the maintenance of imprinted X inactivation in the trophectoderm lineage in mouse. Here we show that recruitment of Eed-Enx1 to the inactive X chromosome (Xi) also occurs in random X inactivation in the embryo proper. Localization of Eed-Enx1 complexes to Xi occurs very early, at the onset of Xist expression, but then disappears as differentiation and development progress. This transient localization correlates with the presence of high levels of the complex in totipotent cells and during early differentiation stages. Functional analysis demonstrates that Eed-Enx1 is required to establish methylation of histone H3 at lysine 9 and/or lysine 27 on Xi and that this, in turn, is required to stabilize the Xi chromatin structure.


Journal article


Dev Cell

Publication Date





481 - 495


Amino Acid Sequence, Animals, Cell Differentiation, Cells, Cultured, Chromatin, DNA Methylation, Dosage Compensation, Genetic, Embryo, Mammalian, Female, Fetus, Gene Expression Regulation, Developmental, Histone-Lysine N-Methyltransferase, Histones, Lysine, Male, Methyltransferases, Mice, Mice, Inbred C57BL, Polycomb Repressive Complex 2, Polycomb-Group Proteins, Protein Methyltransferases, RNA, Long Noncoding, RNA, Untranslated, Repressor Proteins, Totipotent Stem Cells, X Chromosome