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Regulation of Transcription Factor NFAT by ADP-Ribosylation
Author(s) -
Opeyemi A. Olabisi,
Noemí Soto-Nieves,
Edward Nieves,
Teddy Yang,
Xiaoyong Yang,
Raymond Yu,
Hee Yun Suk,
Fernando Macián,
ChiWing Chow
Publication year - 2008
Publication title -
molecular and cellular biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.14
H-Index - 327
eISSN - 1067-8824
pISSN - 0270-7306
DOI - 10.1128/mcb.01746-07
Subject(s) - nfat , biology , transcription factor , poly adp ribose polymerase , adp ribosylation , microbiology and biotechnology , transcription (linguistics) , dna , genetics , biochemistry , gene , polymerase , enzyme , nad+ kinase , linguistics , philosophy
ADP-ribosylation is a reversible posttranslational modification mediated by poly-ADP-ribose polymerase (PARP). The results of recent studies demonstrate that ADP-ribosylation contributes to transcription regulation. Here, we report that transcription factor NFAT binds to and is ADP-ribosylated by PARP-1 in an activation-dependent manner. Mechanistically, ADP-ribosylation increases NFAT DNA binding. Functionally, NFAT-mediated interleukin-2 (IL-2) expression was reduced in T cells upon genetic ablation or pharmacological inhibition of PARP-1. Parp-1(-/-) T cells also exhibit reduced expression of other NFAT-dependent cytokines, such as IL-4. Together, these results demonstrate that ADP-ribosylation mediated by PARP-1 provides a molecular switch to positively regulate NFAT-dependent cytokine gene transcription. These results also imply that, similar to the effect of calcineurin inhibition, PARP-1 inhibition may be beneficial in modulating immune functions.

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