Growth factor pleiotropy is controlled by a receptor Tyr/Ser motif that acts as a binary switch

Mark A. Guthridge, Jason A. Powell, Emma F. Barry, Frank C. Stomski, Barbara J. McClure, Hayley Ramshaw, Fernando A. Felquer, Mara Dottore, Daniel T. Thomas, Bik To, C. Glenn Begley, Angel F. Lopez

Research output: Contribution to journalArticle

52 Citations (Scopus)

Abstract

Pleiotropism is a hallmark of cytokines and growth factors; yet, the underlying mechanisms are not clearly understood. We have identified a motif in the granulocyte macrophage-colony-stimulating factor receptor composed of a tyrosine and a serine residue that functions as a binary switch for the independent regulation of multiple biological activities. Signalling occurs either through Ser585 at lower cytokine concentrations, leading to cell survival only, or through Tyr577 at higher cytokine concentrations, leading to cell survival as well as proliferation, differentiation or functional activation. The phosphorylation of Ser585 and Tyr577 is mutually exclusive and occurs via a unidirectional mechanism that involves protein kinase A and tyrosine kinases, respectively, and is deregulated in at least some leukemias. We have identified similar Tyr/Ser motifs in other cell surface receptors, suggesting that such signalling switches may play important roles in generating specificity and pleiotropy in other biological systems.

Original languageEnglish
Pages (from-to)479-489
Number of pages11
JournalEMBO Journal
Volume25
Issue number3
DOIs
Publication statusPublished - 8 Feb 2006

Keywords

  • 14-3-3
  • Cell proliferation
  • Cell survival
  • Cytokine
  • Receptors

ASJC Scopus subject areas

  • Neuroscience(all)
  • Molecular Biology
  • Immunology and Microbiology(all)
  • Biochemistry, Genetics and Molecular Biology(all)

Cite this

Guthridge, M. A., Powell, J. A., Barry, E. F., Stomski, F. C., McClure, B. J., Ramshaw, H., ... Lopez, A. F. (2006). Growth factor pleiotropy is controlled by a receptor Tyr/Ser motif that acts as a binary switch. EMBO Journal, 25(3), 479-489. https://doi.org/10.1038/sj.emboj.7600948