1. Academic Validation
  2. TRIM8 modulates STAT3 activity through negative regulation of PIAS3

TRIM8 modulates STAT3 activity through negative regulation of PIAS3

  • J Cell Sci. 2010 Jul 1;123(Pt 13):2238-45. doi: 10.1242/jcs.068981.
Fumihiko Okumura 1 Yui Matsunaga Yuta Katayama Keiichi I Nakayama Shigetsugu Hatakeyama
Affiliations

Affiliation

  • 1 Department of Biochemistry, Hokkaido University Graduate School of Medicine, N15, W7, Kita-ku, Sapporo, Hokkaido 060-8638, Japan.
Abstract

TRIM8 is a member of the protein family defined by the presence of a common domain structure composed of a tripartite motif: a RING-finger, one or two B-box domains and a coiled-coil motif. Here, we show that TRIM8 interacts with protein inhibitor of activated STAT3 (PIAS3), which inhibits IL-6-dependent activation of STAT3. Ectopic expression of TRIM8 cancels the negative effect of PIAS3 on STAT3, either by degradation of PIAS3 through the ubiquitin-proteasome pathway or exclusion of PIAS3 from the nucleus. Furthermore, expression of TRIM8 in NIH3T3 cells enhances Src-dependent tumorigenesis. These findings indicate that TRIM8 enhances the STAT3-dependent signal pathway by inhibiting the function of PIAS3.

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