The role of YAP transcription coactivator in regulating stem cell self-renewal and differentiation

Ian Lian, Joungmok Kim, Hideki Okazawa, Jiagang Zhao, Bin Zhao, Jindan Yu, Arul Chinnaiyan, Mason A. Israel, Lawrence S.B. Goldstein, Ramzey Abujarour, Sheng Ding, Kun Liang Guan*

*Corresponding author for this work

Research output: Contribution to journalArticle

395 Scopus citations

Abstract

Yes-associated protein (YAP) is a potent transcription coactivator acting via binding to the TEAD transcription factor, and plays a critical role in organ size regulation. YAP is phosphorylated and inhibited by the Lats kinase, a key component of the Hippo tumor suppressor pathway. Elevated YAP protein levels and gene amplification have been implicated in human cancer. In this study, we report that YAP is inactivated during embryonic stem (ES) cell differentiation, as indicated by decreased protein levels and increased phosphorylation. Consistently, YAP is elevated during induced pluripotent stem (iPS) cell reprogramming. YAP knockdown leads to a loss of ES cell pluripotency, while ectopic expression of YAP prevents ES cell differentiation in vitro and maintains stem cell phenotypes even under differentiation conditions. Moreover, YAP binds directly to promoters of a large number of genes known to be important for stem cells and stimulates their expression. Our observations establish a critical role of YAP in maintaining stem cell pluripotency.

Original languageEnglish (US)
Pages (from-to)1106-1118
Number of pages13
JournalGenes and Development
Volume24
Issue number11
DOIs
StatePublished - Jun 1 2010

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Keywords

  • Hippo
  • Stem cells
  • TEAD
  • YAP

ASJC Scopus subject areas

  • Genetics
  • Developmental Biology

Cite this

Lian, I., Kim, J., Okazawa, H., Zhao, J., Zhao, B., Yu, J., Chinnaiyan, A., Israel, M. A., Goldstein, L. S. B., Abujarour, R., Ding, S., & Guan, K. L. (2010). The role of YAP transcription coactivator in regulating stem cell self-renewal and differentiation. Genes and Development, 24(11), 1106-1118. https://doi.org/10.1101/gad.1903310