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The multifunctional protein PEA-15 is involved in the control of apoptosis and cell cycle in astrocytes

  • François Renault
  • , Etienne Formstecher
  • , Isabelle Callebaut
  • , Marie Pierre Junier
  • , Hervé Chneiweiss
  • INSERM U869
  • Université Pierre et Marie Curie

Research output: Contribution to journalArticlepeer-review

Abstract

PEA-15 is a small protein (15kDa) that was first identified as an abundant phosphoprotein in brain astrocytes [Araujo et al., J Biol Chem 1993;268(8):5911-20], and subsequently shown to be widely expressed in different tissues and highly conserved among mammals [Estelles et al., J Biol Chem 1996;271(25):14800-6; Danziger et al., J Neurochem 1995;64(3):1016-25]. It is composed of a N-terminal death effector domain and a C-terminal tail of irregular structure. PEA-15 is regulated by multiple calcium-dependent phosphorylation pathways that account for its different forms: a non-phosphorylated form in equilibrium with a mono and a biphosphorylated variety. This already suggested that PEA-15 may play a major role in signal integration. Accordingly, it has been demonstrated to modulate signaling pathways that control apoptosis and cell proliferation. In particular, PEA-15 diverts astrocytes from TNFalpha-triggered apoptosis and regulates the actions of the ERK MAP kinase cascade by binding to ERK and altering its subcellular localization. The three-dimensional structure of PEA-15 has been modelized and recently determined using NMR spectroscopy, and may help to understand the various functions played by the protein through its molecular interactions.

Original languageEnglish
Pages (from-to)1581-1588
Number of pages8
JournalBiochemical Pharmacology
Volume66
Issue number8
DOIs
Publication statusPublished - 15 Oct 2003
Externally publishedYes

Keywords

  • CaMKII
  • Calcium-calmodulin-dependent kinase type II
  • DED
  • Death effector domain
  • ERK MAP kinase
  • Extracellular regulated kinase mitogen-associated protein kinase
  • FADD
  • NMR
  • Nuclear magnetic resonance
  • PKC
  • Protein kinase C
  • TNFalpha
  • Tumor necrosis factor alpha

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