| Literature DB >> 25861992 |
Hiroyuki Hosokawa1, Miki Kato1, Hiroyuki Tohyama1, Yuuki Tamaki1, Yusuke Endo1, Motoko Y Kimura1, Damon John Tumes1, Shinichiro Motohashi2, Masaki Matsumoto3, Keiichi I Nakayama3, Tomoaki Tanaka4, Toshinori Nakayama5.
Abstract
Gata3 acts as a master regulator for T helper 2 (Th2) cell differentiation by inducing chromatin remodeling of the Th2 cytokine loci, accelerating Th2 cell proliferation, and repressing Th1 cell differentiation. Gata3 also directly transactivates the interleukin-5 (Il5) gene via additional mechanisms that have not been fully elucidated. We herein identified a mechanism whereby the methylation of Gata3 at Arg-261 regulates the transcriptional activation of the Il5 gene in Th2 cells. Although the methylation-mimicking Gata3 mutant retained the ability to induce IL-4 and repress IFNγ production, the IL-5 production was selectively impaired. We also demonstrated that heat shock protein (Hsp) 60 strongly associates with the methylation-mimicking Gata3 mutant and negatively regulates elongation of the Il5 transcript by RNA polymerase II. Thus, arginine methylation appears to play a pivotal role in the organization of Gata3 complexes and the target gene specificity of Gata3.Entities:
Keywords: GATA transcription factor; Gata3; Hsp60; IL-5; T helper cells; Th2; post-translational modification (PTM); protein methylation; transcription factor
Mesh:
Substances:
Year: 2015 PMID: 25861992 PMCID: PMC4505565 DOI: 10.1074/jbc.M114.621524
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157