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Comment
. 2009 Jun 1;185(5):761-3.
doi: 10.1083/jcb.200904125.

Epigenetics, Wnt signaling, and stem cells: the Pygo2 connection

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Comment

Epigenetics, Wnt signaling, and stem cells: the Pygo2 connection

Valerie Horsley. J Cell Biol. .

Abstract

Stem cells use both transcriptional and epigenetic mechanisms to control gene expression and regulate tissue development and homeostasis. In this issue, Gu et al. (Gu, B., P. Sun, Y. Yuan, R.C. Moraes, A. Li, A. Teng, A. Agrawal, C. Rhéaume, V. Bilanchone, J.M. Veltmaat, et al. 2009. J. Cell Biol. 185:811-826) reveal an important link between these two mechanisms in mammary epithelial stem cells by showing that transcriptional activation of beta-catenin downstream of Wnt signaling can be regulated epigenetically through a chromatin remodeling factor, Pygo2.

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Figures

Figure 1.
Figure 1.
Pygo2 regulates Wnt signaling during mammary gland development. Pygo2 promotes trimethylation (yellow) of lysine 4 of histone H3 (H3K4) and synergistically binds these residues and BCL9–β-catenin complexes to activate β-catenin target genes in mammary epithelium. Loss of Pygo2 in mice results in embryonic defects of mammary progenitor cells and placode (white circle) formation. In addition, loss of Pygo2 results in postnatal defects in mammary ductal networks caused by the lack of stem cells in TEBs (purple circles). Pygo2-null mammary glands rescue mammary overgrowth phenotypes when Wnt signaling is hyperactivated.

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