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The transcription factor NF-AT responds to Ca2+-calcineurin signals by translocating to the nucleus, where it participates in the activation of early immune response genes. Calcineurin dephosphorylates conserved serine residues in the amino terminus of NF-AT, resulting in nuclear import. Purification of the NF-AT kinase revealed that it is composed of a priming kinase activity and glycogen synthase kinase-3 (GSK-3). GSK-3 phosphorylates conserved serines necessary for nuclear export, promotes nuclear exit, and thereby opposes Ca2+-calcineurin signaling. Because GSK-3 responds to signals initiated by Wnt and other ligands, NF-AT family members could be effectors of these pathways.
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Chan Beals
Merck & Co., Inc., Rahway, NJ, USA (United States)
Colleen M. Sheridan
University of Washington
Christoph W. Turck
Kunming Institute of Zoology
Science
Stanford University
Howard Hughes Medical Institute
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Beals et al. (Fri,) studied this question.
synapsesocial.com/papers/6a204ca6a1e2f4aec32ed480 — DOI: https://doi.org/10.1126/science.275.5308.1930
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