Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1996 Aug 20;93(17):8907-12.
doi: 10.1073/pnas.93.17.8907.

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

Affiliations

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

C Luo et al. Proc Natl Acad Sci U S A. .

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.

PubMed Disclaimer

References

    1. Nucleic Acids Res. 1990 Sep 11;18(17):5322 - PubMed
    1. EMBO J. 1990 Dec;9(13):4425-33 - PubMed
    1. Nucleic Acids Res. 1991 Jan 11;19(1):61-7 - PubMed
    1. Cell. 1991 Aug 23;66(4):807-15 - PubMed
    1. Nature. 1991 Aug 29;352(6338):803-7 - PubMed

Publication types

MeSH terms

LinkOut - more resources