Interaction of calcineurin with a domain of the transcription factor NFAT1 that controls nuclear import

  1. C Luo,
  2. K T Shaw,
  3. A Raghavan,
  4. J Aramburu,
  5. F Garcia-Cozar,
  6. B A Perrino,
  7. P G Hogan, and
  8. A Rao
  1. Division of Cellular and Molecular Biology, Dana-Farber Cancer Institute, Boston, MA 02115, USA.

Abstract

The nuclear import of the nuclear factor of activated T cells (NFAT)-family transcription factors is initiated by the protein phosphatase calcineurin. Here we identify a regulatory region of NFAT1, N terminal to the DNA-binding domain, that controls nuclear import of NFAT1. The regulatory region of NFAT1 binds directly to calcineurin, is a substrate for calcineurin in vitro, and shows regulated subcellular localization identical to that of full-length NFAT1. The corresponding region of NFATc likewise binds calcineurin, suggesting that the efficient activation of NFAT1 and NFATc by calcineurin reflects a specific targeting of the phosphatase to these proteins. The presence in other NFAT-family transcription factors of several sequence motifs from the regulatory region of NFAT1, including its probable nuclear localization sequence, indicates that a conserved protein domain may control nuclear import of all NFAT proteins.

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