TIFAB inhibits TIFA, TRAF-interacting protein with a forkhead-associated domain

Takayuki Matsumura, Kentaro Semba, Sakura Azuma, Shuntaro Ikawa, Jin Gohda, Taishin Akiyama, Jun Ichiro Inoue*

*この研究の対応する著者

研究成果: Article査読

14 被引用数 (Scopus)

抄録

Tumor necrosis factor receptor-associated factor 6 (TRAF6) transduces signals that lead to activation of NFκB and AP-1, which is essential for cell differentiation and establishment of the immune and inflammatory systems. TRAF-interacting protein with a forkhead-associated domain (TIFA) was identified as a TRAF6-binding protein that could link IRAK-1 to TRAF6 and then activate TRAF6 upon stimulation. We report identification of a TIFA-related protein, TIFAB, that inhibits TIFA-mediated activation of NFκB. TIFAB does not associate with members of the TRAF family but does bind TIFA. We analyzed the effect of TIFAB expression on the TRAF6/TIFA interaction by immunoprecipitation of TRAF6 and found that TIFA coprecipitated with TRAF6 was not changed. However, when we analyzed this interaction by immunoprecipitation of TIFA, we found that TIFAB significantly increased the amount of TRAF6 coprecipitated with TIFA. These findings suggest that TIFAB inhibits the TIFA-mediated TRAF6 activation possibly by inducing a conformational change in TIFA.

本文言語English
ページ(範囲)230-234
ページ数5
ジャーナルBiochemical and Biophysical Research Communications
317
1
DOI
出版ステータスPublished - 2004 4 23
外部発表はい

ASJC Scopus subject areas

  • 生物理学
  • 生化学
  • 分子生物学
  • 細胞生物学

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