The Tumor Suppressor hTid1 Inhibits STAT5b Activity via Functional Interaction*

  1. Fabrice Gouilleux4,6
  1. From the INSERM (U925), Université de Picardie Jules Verne, UFR de Médecine, 3 Rue des Louvels, 80036 Amiens, France
  1. 5 To whom correspondence may be addressed. Tel.: 33-3-82-79-06; Fax: 33-3-22-82-79-07; E-mail: kaiss.lassoued{at}sa.u-picardie.fr.
  2. 6 To whom correspondence may be addressed: CNRS UMR 6239, GICC, Université F. Rabelais, Faculté de Médecine, 10 bd Tonnellé, 37032 Tours, France. Tel.: 33-247-36-60-79; Fax: 33-247-36-60-95; E-mail: fabrice.gouilleux{at}univ-tours.fr.
  1. 1 Both authors contributed equally to this work.

  2. 4 Both authors contributed equally to this work.

  • 3 Present address: CNRS (UMR 6239), Université F. Rabelais, Faculté de Médecine, 10 Boulevard Tonnellé, 37032 Tours, France.

Abstract

STAT5a and -5b (signal transducers and activators of transcription 5a and 5b) proteins play an essential role in hematopoietic cell proliferation and survival and are frequently constitutively active in hematologic neoplasms and solid tumors. Because STAT5a and STAT5b differ mainly in the carboxyl-terminal transactivation domain, we sought to identify new proteins that bind specifically to this domain by using a bacterial two-hybrid screening. We isolated hTid1, a human DnaJ protein that acts as a tumor suppressor in various solid tumors. hTid1 interacts specifically with STAT5b but not with STAT5a in hematopoietic cell lines. This interaction involves the cysteine-rich region of the hTid1 DnaJ domain. We also demonstrated that hTid1 negatively regulates the expression and transcriptional activity of STAT5b and suppresses the growth of hematopoietic cells transformed by an oncogenic form of STAT5b. Our findings define hTid1 as a novel partner and negative regulator of STAT5b.

Footnotes

  • 2 Supported by the “Ministere de la Recherche.”

  • * This work was supported by INSERM, Association de la Recherche contre le Cancer, Ligue contre le Cancer, Conseil Régional de Picardie.

  • Graphic The on-line version of this article (available at http://www.jbc.org) contains supplemental Figs. 1 and 2.

  • Received June 18, 2010.
  • Revision received November 15, 2010.
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