scholarly journals Identification of Two Nuclear Factor of Activated T-cells (NFAT)-response Elements in the 5′-Upstream Regulatory Region of the ET-1 Promoter

2010 ◽  
Vol 285 (37) ◽  
pp. 28520-28528 ◽  
Author(s):  
Kevin A. Strait ◽  
Peter K. Stricklett ◽  
Rachel M. Kohan ◽  
Donald E. Kohan
1996 ◽  
Vol 184 (1) ◽  
pp. 141-147 ◽  
Author(s):  
C Luo ◽  
E Burgeon ◽  
A Rao

Nuclear factor of activated T cells-family proteins (NFAT1/NFATp, NFATc, NFAT3, and NFAT4/NFATx/NFATc3) play a key role in the transcription of cytokine genes and other genes during the immune response. We have defined the mechanisms of transactivation by NFAT1. NFAT1 possesses two transactivation domains whose sequences are not conserved in the other NFAT-family proteins, and a conserved DNA-binding domain that mediates the recruitment of cooperating nuclear transcription factors even when it is expressed in the absence of other regions of the protein. The activity of the NH2-terminal transactivation domain is modulated by an adjacent regulatory region that contains several conserved sequence motifs represented only in the NFAT family. Our results emphasize the multiple levels at which NFAT-dependent transactivation is regulated, and predict significant differences in the architecture of cooperative transcription complexes containing different NFAT-family proteins.


2000 ◽  
Vol 20 (2) ◽  
pp. 702-712 ◽  
Author(s):  
Chi-Wing Chow ◽  
Roger J. Davis

ABSTRACT Calcium-stimulated nuclear factor of activated T cells (NFAT) transcription activity at the interleukin-2 promoter is negatively regulated by cyclic AMP (cAMP). This effect of cAMP is mediated, in part, by protein kinase A phosphorylation of NFAT. The mechanism of regulation involves the creation of a phosphorylation-dependent binding site for 14-3-3. Decreased NFAT phosphorylation caused by the calcium-stimulated phosphatase calcineurin, or mutation of the PKA phosphorylation sites, disrupted 14-3-3 binding and increased NFAT transcription activity. In contrast, NFAT phosphorylation caused by cAMP increased 14-3-3 binding and reduced NFAT transcription activity. The regulated interaction between NFAT and 14-3-3 provides a mechanism for the integration of calcium and cAMP signaling pathways.


Author(s):  
Meredith J. Giblin ◽  
Taylor E. Smith ◽  
Garrett Winkler ◽  
Hannah A. Pendergrass ◽  
Minjae J. Kim ◽  
...  

2006 ◽  
Vol 103 (10) ◽  
pp. 3740-3745 ◽  
Author(s):  
T. So ◽  
J. Song ◽  
K. Sugie ◽  
A. Altman ◽  
M. Croft

Diabetologia ◽  
2011 ◽  
Vol 54 (10) ◽  
pp. 2690-2701 ◽  
Author(s):  
C. Goettsch ◽  
M. Rauner ◽  
C. Hamann ◽  
K. Sinningen ◽  
U. Hempel ◽  
...  

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