Nuclear Accumulation of NFAT4 Opposed by the JNK Signal Transduction Pathway

Author:

Chow Chi-Wing12,Rincón Mercedes12,Cavanagh Julie12,Dickens Martin12,Davis Roger J.12

Affiliation:

1. C.-W. Chow, J. Cavanagh, M. Dickens, R. J. Davis, Howard Hughes Medical Institute, Program in Molecular Medicine, Department of Biochemistry and Molecular Biology, University of Massachusetts Medical School, Worcester, MA 01605, USA.

2. M. Rincón, Program in Immunobiology, Department of Medicine, University of Vermont, Burlington, VT 05405, USA.

Abstract

The nuclear factor of activated T cells (NFAT) group of transcription factors is retained in the cytoplasm of quiescent cells. NFAT activation is mediated in part by induced nuclear import. This process requires calcium-dependent dephosphorylation of NFAT caused by the phosphatase calcineurin. The c-Jun amino-terminal kinase (JNK) phosphorylates NFAT4 on two sites. Mutational removal of the JNK phosphorylation sites caused constitutive nuclear localization of NFAT4. In contrast, JNK activation in calcineurin-stimulated cells caused nuclear exclusion of NFAT4. These findings show that the nuclear accumulation of NFAT4 promoted by calcineurin is opposed by the JNK signal transduction pathway.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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