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  Lineage regulators direct BMP and Wnt pathways to cell-specific programs during differentiation and regeneration

Trompouki, E., Bowman, T. V., Lawton, L. N., Fan, Z. P., Wu, D.-C., DiBiase, A., et al. (2011). Lineage regulators direct BMP and Wnt pathways to cell-specific programs during differentiation and regeneration. Cell, 147, 577-589. doi:10.1016/j.cell.2011.09.044.

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Trompouki et al..pdf (Publisher version), 991KB
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Trompouki, Eirini1, Author           
Bowman, Teresa V.2, Author
Lawton, Lee N.2, Author
Fan, Zi Peng2, Author
Wu, Dai-Chen2, Author
DiBiase, Anthony2, Author
Martin, Corey S.2, Author
Cech, Jennifer N.2, Author
Sessa, Anna K.2, Author
Leblanc, Jocelyn L.2, Author
Li, Pulin2, Author
Durand, Ellen M.2, Author
Mosimann, Christian2, Author
Heffner, Garrett C.2, Author
Daley, George Q.2, Author
Paulson, Robert F.2, Author
Young, Richard A.2, Author
Zon, Leonard I.2, Author
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1Max Planck Institute of Immunobiology and Epigenetics, Max Planck Society, ou_2243641              
2External Organizations, ou_persistent22              

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 Abstract: BMP and Wnt signaling pathways control essential cellular responses through activation of the transcription factors SMAD (BMP) and TCF (Wnt). Here, we show that regeneration of hematopoietic lineages following acute injury depends on the activation of each of these signaling pathways to induce expression of key blood genes. Both SMAD1 and TCF7L2 co-occupy sites with master regulators adjacent to hematopoietic genes. In addition, both SMAD1 and TCF7L2 follow the binding of the predominant lineage regulator during differentiation from multipotent hematopoietic progenitor cells to erythroid cells. Furthermore, induction of the myeloid lineage regulator C/EBPα in erythroid cells shifts binding of SMAD1 to sites newly occupied by C/EBPα, whereas expression of the erythroid regulator GATA1 directs SMAD1 loss on nonerythroid targets. We conclude that the regenerative response mediated by BMP and Wnt signaling pathways is coupled with the lineage master regulators to control the gene programs defining cellular identity.

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Language(s): eng - English
 Dates: 2011
 Publication Status: Issued
 Pages: -
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 Rev. Type: Peer
 Identifiers: DOI: 10.1016/j.cell.2011.09.044
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Title: Cell
Source Genre: Journal
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Publ. Info: Cambridge, Mass. : Cell Press
Pages: - Volume / Issue: 147 Sequence Number: - Start / End Page: 577 - 589 Identifier: ISSN: 0092-8674
CoNE: https://pure.mpg.de/cone/journals/resource/954925463183