PIASy, a nuclear matrix–associated SUMO E3 ligase, represses LEF1 activity by sequestration into nuclear bodies

  1. Shrikesh Sachdev1,
  2. Laurakay Bruhn1,
  3. Heidemarie Sieber1,
  4. Andrea Pichler2,
  5. Frauke Melchior2, and
  6. Rudolf Grosschedl1,3
  1. 1Gene Center and Institute of Biochemistry, University of Munich, 81377 Munich, Germany; and 2Max-Planck Institute of Biochemistry, 82152 Martinsried, Germany

Abstract

The Wnt-responsive transcription factor LEF1 can activate transcription in association with β-catenin and repress transcription in association with Groucho. In search of additional regulatory mechanisms of LEF1 function, we identified the protein inhibitor of activated STAT, PIASy, as a novel interaction partner of LEF1. Coexpression of PIASy with LEF1 results in potent repression of LEF1 activity and in covalent modification of LEF1 with SUMO. PIASy markedly stimulates the sumoylation of LEF1 and multiple other proteins in vivo and functions as a SUMO E3 ligase for LEF1 in a reconstituted system in vitro. Moreover, PIASy binds to nuclear matrix–associated DNA sequences and targets LEF1 to nuclear bodies, suggesting that PIASy-mediated subnuclear sequestration accounts for the repression of LEF1 activity.

Keywords

Footnotes

  • 3 Corresponding author.

  • E-MAIL rgross{at}lmb.uni-muenchen.de; FAX 49-89-2180-6949.

  • Article and publication are at http://www.genesdev.org/cgi/doi/10.1101/gad.944801.

    • Received September 14, 2001.
    • Accepted October 17, 2001.
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