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Receptor specific downregulation of cytokine signaling by autophosphorylation in the FERM domain of Jak2
Author(s) -
FunakoshiTago Megumi,
Pelletier Stephane,
Matsuda Tadashi,
Parganas Evan,
Ihle James N
Publication year - 2006
Publication title -
the embo journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.484
H-Index - 392
eISSN - 1460-2075
pISSN - 0261-4189
DOI - 10.1038/sj.emboj.7601365
Subject(s) - memphis , library science , autophosphorylation , medicine , biology , protein kinase a , biochemistry , botany , computer science , enzyme
The tyrosine kinase, Janus kinase‐2 (Jak2), plays a pivotal role in signal transduction through a variety of cytokine receptors, including the receptor for erythropoietin (Epo). Although the physiological relevance of Jak2 has been definitively established, less is known about its regulation. In studies assessing the roles of sites of tyrosine phosphorylation, we identified Y 119 in the FERM (band 4.1, Ezrin, radixin and moesin) domain as a phosphorylation site. In these studies, we demonstrate that the phosphorylation of Y 119 in response to Epo downregulates Jak2 kinase activity. Using a phosphorylation mimic mutation (Y 119 E), downregulation is shown to involve dissociation of Jak2 from the receptor complex. Conversely, a Y 119 F mutant is more stably associated with the receptor complex. Thus, in cytokine responses, ligand binding induces activation of receptor associated Jak2, autophosphorylation of Y 119 in the FERM domain and the subsequent dissociation of the activated Jak2 from the receptor and degradation. This regulation occurs with the receptors for Epo, thrombopoietin and growth hormone but not with the receptor for interferon‐γ.