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Volume 271, Number 29, Issue of July 19, 1996 pp. 17174-17182
©1996 by The American Society for Biochemistry and Molecular Biology, Inc.

Other Kinases Can Substitute for Jak2 in Signal Transduction by Interferon-gamma

(Received for publication, February 12, 1996, and in revised form, May 3, 1996)

Serguei V. Kotenko , Lara S. Izotova , Brian P. Pollack , Geetha Muthukumaran , Kirsi Paukku Dagger , Olli Silvennoinen Dagger , James N. Ihle § and Sidney Pestka

From the Department of Molecular Genetics and Microbiology, University of Medicine and Dentistry of New Jersey, Robert Wood Johnson Medical School, Piscataway, New Jersey 08854-5635, the Dagger  Department of Virology, University of Helsinki, Helsinki, Finland, and the § Department of Biochemistry, St. Jude Children's Hospital, Memphis, Tennessee 38105

Each cytokine which utilizes the Jak-Stat signal transduction pathway activates a distinct combination of members of the Jak and Stat families. Thus, either the Jaks, the Stats, or both could contribute to the specificity of ligand action. With the use of chimeric receptors involving the interferon gamma  receptor (IFN-gamma R) complex as a model system, we demonstrate that Jak2 activation is not an absolute requirement for IFN-gamma signaling. Other members of the Jak family can functionally substitute for Jak2. IFN-gamma can signal through the activation of Jak family members other than Jak2 as measured by Statlalpha homodimerization and major histocompatibility complex class I antigen expression. This indicates that Jaks are interchangeable and indiscriminative in the Jak-Stat signal transduction pathway. The necessity for the activation of one particular kinase during signaling can be overcome by recruiting another kinase to the receptor complex. The results may suggest that the Jaks do not contribute to the specificity of signal transduction in the Jak-Stat pathway to the same degree as Stats.


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