MEKK1 binds HECT E3 ligase itch by its amino-terminal RING motif to regulate Th2 cytokine gene expression

Thomas Enzler, Xing Chang, Valeria Facchinetti, Gerry Melino, Michael Karin, Bing Su, Ewen Gallagher

Research output: Contribution to journalArticlepeer-review

Abstract

MEKK1-dependent signaling regulates HECT E3 ligase Itch, resulting in elevated catalytic activity. After TCR costimulation, MEKK1 predominantly induces JNK1 activation, whereas the related kinase MEKK2 regulates ERK5 activation. MEKK1 becomes phosphorylated on multiple sites and polyubiquitinated following TCR costimulation. E3 ligase Itch is recruited to activated MEKK1, but not MEKK2, and this novel scaffolding interaction is dependent on MEKK1 Thr1381 phosphorylation within the kinase domain and an intact MEKK1 RING finger motif. MEKK1 phosphorylation on Thr1381 is observed during Th2 differentiation, but not under Th1 differentiation. Both Itch and the MEKK1 kinase domain are important for Il4 and Il6 cytokine gene expression under Th2 conditions.

Original languageEnglish
Pages (from-to)3831-3838
Number of pages8
JournalJournal of Immunology
Volume183
Issue number6
DOIs
Publication statusPublished - Sep 15 2009

ASJC Scopus subject areas

  • Immunology
  • Medicine(all)

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