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Originally published In Press as doi:10.1074/jbc.C500138200 on April 29, 2005

J. Biol. Chem., Vol. 280, Issue 24, 22788-22792, June 17, 2005
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Identification of an Acquired JAK2 Mutation in Polycythemia Vera*

Runxiang Zhao{ddagger}, Shu Xing{ddagger}§, Zhe Li{ddagger}§, Xueqi Fu§, Qingshan Li§, Sanford B. Krantz{ddagger}, and Zhizhuang Joe Zhao{ddagger}§

From the {ddagger}Hematology/Oncology Division, Department of Medicine, Vanderbilt-Ingram Cancer Center, Vanderbilt University, Nashville, Tennessee 37232 and the §Edmond H. Fischer Signal Transduction Laboratory, College of Life Sciences, Jilin University, Changchun 130023, China

Polycythemia vera (PV) is a human clonal hematological disorder. The molecular etiology of the disease has not been identified. PV hematopoietic progenitor cells exhibit hypersensitivity to growth factors and cytokines, suggesting possible abnormalities in protein-tyrosine kinases and phosphatases. By sequencing the entire coding regions of cDNAs of candidate enzymes, we identified a G:C-> T:A point mutation of the JAK2 tyrosine kinase in 20 of 24 PV blood samples but none in 12 normal samples. The mutation has varying degrees of heterozygosity and is apparently acquired. It changes conserved Val617 to Phe in the pseudokinase domain of JAK2 that is known to have an inhibitory role. The mutant JAK2 has enhanced kinase activity, and when overexpressed together with the erythropoietin receptor in cells, it caused hyperactivation of erythropoietin-induced cell signaling. This gain-of-function mutation of JAK may explain the hypersensitivity of PV progenitor cells to growth factors and cytokines. Our study thus defines a molecular defect of PV.


Received for publication, March 25, 2005 , and in revised form, April 26, 2005.

* This work was supported by Grants HL076309 (to Z. J. Z.), DK-15555 (to S. B. K.), and CA-68485 (to Vanderbilt-Ingram Cancer Center) from the National Institutes of Health. The costs of publication of this article were defrayed in part by the payment of page charges. This 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: 777 Preston Research Bldg., 2220 Pierce Ave., Nashville, TN 37232. Fax: 615-936-3853; Tel.: 615-936-1797; E-mail: joe.zhao{at}vanderbilt.edu.


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Identification of an Acquired Mutation in Jak2 Provides Molecular Insights into the Pathogenesis of Myeloproliferative Disorders
Mol. Interv., August 1, 2005; 5(4): 211 - 215.
[Abstract] [Full Text] [PDF]


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ASH Education BookHome page
W. Vainchenker and S. N. Constantinescu
A Unique Activating Mutation in JAK2 (V617F) Is at the Origin of Polycythemia Vera and Allows a New Classification of Myeloproliferative Diseases
Hematology, January 1, 2005; 2005(1): 195 - 200.
[Abstract] [Full Text] [PDF]




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