TEAD/TEF transcription factors utilize the activation domain of YAP65, a Src/Yes-associated protein localized in the cytoplasm

  1. Alex Vassilev,
  2. Kotaro J. Kaneko,
  3. Hongjun Shu1,
  4. Yingming Zhao1, and
  5. Melvin L. DePamphilis2
  1. National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20892-2753, USA;1Department of Biochemistry, University of Texas Southwestern Medical Center, Dallas, Texas 75390-9038, USA

Abstract

Mammals express four highly conserved TEAD/TEF transcription factors that bind the same DNA sequence, but serve different functions during development. TEAD-2/TEF-4 protein purified from mouse cells was associated predominantly with a novel TEAD-binding domain at the amino terminus of YAP65, a powerful transcriptional coactivator. YAP65 interacted specifically with the carboxyl terminus of all four TEAD proteins. Both this interaction and sequence-specific DNA binding by TEAD were required for transcriptional activation in mouse cells. Expression of YAP in lymphocytic cells that normally do not support TEAD-dependent transcription (e.g., MPC11) resulted in up to 300-fold induction of TEAD activity. Conversely, TEAD overexpression squelched YAP activity. Therefore, the carboxy-terminal acidic activation domain in YAP is the transcriptional activation domain for TEAD transcription factors. However, whereas TEAD was concentrated in the nucleus, excess YAP65 accumulated in the cytoplasm as a complex with the cytoplasmic localization protein, 14-3-3. Because TEAD-dependent transcription was limited by YAP65, and YAP65 also binds Src/Yes protein tyrosine kinases, we propose that YAP65 regulates TEAD-dependent transcription in response to mitogenic signals.

Keywords

Footnotes

  • 2 Corresponding author.

  • E-MAIL depamphm{at}mail.nih.gov; FAX (301) 480-9354.

  • Article and publication are at www.genesdev.org/cgi/doi/10.1101/gad.888601.

    • Received February 15, 2001.
    • Accepted March 22, 2001.
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