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Vol. 9, Issue 12, 3299-3308, December 1998
*Department of Molecular and Developmental Biology, Janus kinase 2 (Jak2) protein tyrosine kinase plays an
important role in interleukin-3- or granulocyte-macrophage
colony-stimulating factor-mediated signal transduction pathways
leading to cell proliferation, activation of early response genes, and
inhibition of apoptosis. However, it is unclear whether Jak2 can
activate these signaling pathways directly without the involvement of
cytokine receptor phosphorylation. To investigate the specific role of
Jak2 in the regulation of signal transduction pathways, we generated
gyrase B (GyrB)-Jak2 fusion proteins, dimerized through the addition of coumermycin. Coumermycin induced autophosphorylation of GyrB-Jak2 fusion proteins, thus bypassing receptor activation. Using different types of chimeric Jak2 molecules, we observed that although the kinase
domain of Jak2 is sufficient for autophosphorylation, the N-terminal
regions are essential for the phosphorylation of Stat5 and for the
induction of short-term cell proliferation. Moreover, coumermycin-induced activation of Jak2 can also lead to increased levels of c-myc and CIS mRNAs in BA/F3 cells stably expressing the Jak2 fusion protein with the intact N-terminal region. Conversely, activation of the chimeric Jak2 induced neither phosphorylation of Shc
or SHP-2 nor activation of the c-fos promoter. Here, we showed
that the GyrB-Jak2 system can serve as an excellent model to dissect
signals of receptor-dependent and -independent events. We also obtained
evidence indicating a role for the N-terminal region of Jak2 in
downstream signaling events.
CREST,
Corresponding author: E-mail address:
sumiko{at}ims.utokyo.ac.jp.
Molecular Biology of the Cell
Vol. 9, 3299-3308, December 1998
Copyright © 1998 by The American Society for Cell Biology
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