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Originally published In Press as doi:10.1074/jbc.M201120200 on April 29, 2002

J. Biol. Chem., Vol. 277, Issue 26, 23544-23553, June 28, 2002
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Studies with Chimeric Mpl/JAK2 Receptors Indicate That Both JAK2 and the Membrane-proximal Domain of Mpl Are Required for Cellular Proliferation*

Jonathan G. DrachmanDagger §, Yoshitaka Miyakawa§||, Jennifer N. LuthiDagger , Debra D. DahlenDagger §, Alexa Raney§, Amy E. Geddis§**, and Kenneth Kaushansky§**

From the Dagger  Puget Sound Blood Center, Seattle, Washington 98104 and the § University of Washington, School of Medicine, Seattle, Washington 98195

The thrombopoietin (TPO) receptor c-Mpl, like other members of the cytokine receptor superfamily, requires the association and activation of Janus kinases (JAKs) for normal signal transduction. The membrane-proximal portion of the signaling domain, containing conserved box1 and box2 motifs, is sufficient to support the proliferation of cytokine-dependent cell lines and basal megakaryocytopoiesis in vivo. We hypothesized that activation of the JAK2 kinase alone might be sufficient for proliferative signaling. To test this premise, we constructed chimeric receptors in which the extracellular and transmembrane portions of Mpl were fused to the pseudokinase and kinase domains of murine JAK2 kinase. When expressed in the interleukin-3-dependent cell line Ba/F3, the chimeric receptors were appropriately expressed on the cell surface and were able to initiate tyrosine kinase activity upon exposure to TPO. However, chimeric receptors lacking an intact box2 domain of Mpl were unable to support proliferation at any concentration of TPO. Only chimeric receptors containing both JAK2 kinase activity and the box2 region initiated proliferative signaling. Within the box2 motif, we determined that the sequence Glu56-Ile57-Leu58 of the Mpl cytoplasmic domain is critical for proliferation of the chimeric receptors. Furthermore, TPO-dependent induction of c-myc transcription is also dependent on this motif. These results indicate that JAK2 activation alone is not sufficient for TPO-induced proliferation and that one or more essential signaling pathways must arise from the cytoplasmic domain of Mpl that includes box2. Although the nature of the signal transduction pathway is not yet known, this second proliferative event is likely to regulate c-myc expression.


* This work was supported by United States Public Health Service Grants K08 HL03498 and R01 HL65498 (to J. G. D.) and Grant R01 CA31615 (to K. K.).The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

To whom correspondence should be addressed: Puget Sound Blood Center, 921 Terry Ave., Seattle, WA 98104. Tel.: 206-292-6510; Fax: 206-343-1776; E-mail: jonathand@psbc.org.

|| Present address: Div. of Hematology, Keio University School of Medicine, Tokyo 160-8582, Japan.

** Present address: Dept. of Medicine, University of California at San Diego, La Jolla, CA 92093.


Copyright © 2002 by The American Society for Biochemistry and Molecular Biology, Inc.
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