Class-specific regulation of pro-inflammatory genes by MyD88 pathways and IκBζ

Hisako Kayama, Vladimir R. Ramirez-Carrozzi, Masahiro Yamamoto, Taketoshi Mizutani, Hirotaka Kuwata, Hideo Iba, Makoto Matsumoto, Kenya Honda, Stephen T. Smale, Kiyoshi Takeda

研究成果: Article査読

84 被引用数 (Scopus)


Toll-like receptors trigger the induction of primary response genes via MyD88-mediated activation of NF-κB and other transcription factors. These factors then act in concert with primary response gene products to induce secondary response genes. Although the MyD88 pathway is important for the expression of both primary and secondary response genes, we show that the recruitment of NF-κB, RNA polymerase, and the TATA-binding protein is MyD88-dependent only at secondary response genes. This selective dependence correlates with the fact that MyD88 is required for nucleosome remodeling and histone H3K4 trimethylation at secondary response promoters, whereas rapidly induced primary response promoters are assembled into poised MyD88-independent chromatin structures. At a subset of secondary response promoters, IκBζ was identified as a selective regulator of H3K4 trimethylation and preinitiation complex assembly after nucleosome remodeling. These mechanistic distinctions advance our understanding of the diverse molecular cascades that underlie the differential regulation of pro-inflammatory genes.

ジャーナルJournal of Biological Chemistry
出版ステータスPublished - 2008 5月 2

ASJC Scopus subject areas

  • 生化学
  • 分子生物学
  • 細胞生物学


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