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

Eirini Trompouki, Teresa V. Bowman, Lee N. Lawton, Zi Peng Fan, Dai Chen Wu, Anthony Dibiase, Corey S. Martin, Jennifer N. Cech, Anna K. Sessa, Jocelyn L. Leblanc, Pulin Li, Ellen M. Durand, Christian Mosimann, Garrett C. Heffner, George Q. Daley, Robert F. Paulson, Richard A. Young, Leonard I. Zon

Research output: Contribution to journalArticle

196 Scopus citations

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.

Original languageEnglish (US)
Pages (from-to)577-589
Number of pages13
JournalCell
Volume147
Issue number3
DOIs
StatePublished - Oct 28 2011

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)

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    Trompouki, E., Bowman, T. V., Lawton, L. N., Fan, Z. P., Wu, D. C., Dibiase, A., Martin, C. S., Cech, J. N., Sessa, A. K., Leblanc, J. L., Li, P., Durand, E. M., Mosimann, C., Heffner, G. C., Daley, G. Q., Paulson, R. F., Young, R. A., & Zon, L. I. (2011). Lineage regulators direct BMP and Wnt pathways to cell-specific programs during differentiation and regeneration. Cell, 147(3), 577-589. https://doi.org/10.1016/j.cell.2011.09.044