TEL/PDGFbetaR fusion protein activates STAT1 and STAT5: a common mechanism for transformation by tyrosine kinase fusion proteins

Exp Hematol. 2000 May;28(5):584-93. doi: 10.1016/s0301-472x(00)00138-7.

Abstract

Objective: TEL/PDGFbetaR is a tyrosine kinase fusion protein associated with the pathogenesis of chronic myelomonocytic leukemia. The following experiments were undertaken to understand the mechanisms whereby TEL/PDGFbetaR transforms cells.

Materials and methods: Activation of JAK and STAT proteins was studied in an interleukin 3 (IL-3)-dependent cell line, Ba/F3, transformed to IL-3 independence by TEL/PDGFbetaR.

Results: TEL/PDGFbetaR activates STAT1 and STAT5 in transformed Ba/F3 cells through a JAK-independent pathway. Activation of STAT proteins requires the kinase activity of TEL/PDGFbetaR. JAK1, JAK2, JAK3, and TYK2 are not phosphorylated by TEL/PDGFbetaR. However, TEL/PDGFbetaR can phosphorylate STAT5 in transiently transfected COS cells, suggesting that TEL/PDGFbetaR may itself be the kinase involved in tyrosine phosphorylation of STAT proteins. In contrast, native PDGFbetaR stimulated by PDGF ligand does not activate STAT proteins to a significant degree in this hematopoietic context. STAT1 and STAT5 also are activated by TEL/ABL and TEL/JAK2 fusion proteins associated with human leukemia.

Conclusions: STAT activation may be a common mechanism of transformation by leukemogenic tyrosine kinase fusion proteins.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Cell Line
  • Cell Line, Transformed
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism*
  • ETS Translocation Variant 6 Protein
  • Enzyme Activation
  • Humans
  • Interferon Type I / pharmacology
  • Interleukin-2 / pharmacology
  • Interleukin-3 / pharmacology*
  • Milk Proteins*
  • Phosphoproteins / metabolism
  • Phosphorylation
  • Phosphotyrosine / analysis
  • Proto-Oncogene Proteins c-ets
  • Receptor, Platelet-Derived Growth Factor beta / genetics
  • Receptor, Platelet-Derived Growth Factor beta / metabolism*
  • Recombinant Fusion Proteins / metabolism
  • Recombinant Proteins
  • Repressor Proteins*
  • STAT1 Transcription Factor
  • STAT5 Transcription Factor
  • Trans-Activators / metabolism*
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*
  • Transfection

Substances

  • DNA-Binding Proteins
  • Interferon Type I
  • Interleukin-2
  • Interleukin-3
  • Milk Proteins
  • Phosphoproteins
  • Proto-Oncogene Proteins c-ets
  • Recombinant Fusion Proteins
  • Recombinant Proteins
  • Repressor Proteins
  • STAT1 Transcription Factor
  • STAT1 protein, human
  • STAT5 Transcription Factor
  • Trans-Activators
  • Transcription Factors
  • Phosphotyrosine
  • Receptor, Platelet-Derived Growth Factor beta