An RNA biding protein, Y14 interacts with and modulates STAT3 activation

Norihiko Ohbayashi, Naohisa Taira, Shiho Kawakami, Sumihito Togi, Noriko Sato, Osamu Ikeda, Shinya Kamitani, Ryuta Muromoto, Yuichi Sekine, Tadashi Matsuda

Research output: Contribution to journalArticlepeer-review

20 Citations (Scopus)

Abstract

Signal transducer and activator of transcription 3 (STAT3), which mediates biological actions in many physiological processes, is activated by cytokines and growth factors via specific tyrosine-phosphorylation, dimerization, and nuclear translocation. To clarify the molecular mechanisms underlying the regulation of STAT3 activation, we performed yeast two-hybrid screening. We identified Y14, an RNA-binding protein, as a novel STAT3 binding partner. Y14 bound to STAT3 through the C-terminal region of STAT3 in vivo. Importantly, small-interfering RNA-mediated reduction of endogenous Y14 expression decreased IL-6-induced tyrosine-phosphorylation, nuclear accumulation, and DNA-binding activity of STAT3, as well as IL-6/STAT3-dependent gene expression. These results indicate that Y14 interacts with STAT3 and regulates the transcriptional activation of STAT3 by influencing the tyrosine-phosphorylation of STAT3.

Original languageEnglish
Pages (from-to)475-479
Number of pages5
JournalBiochemical and biophysical research communications
Volume372
Issue number3
DOIs
Publication statusPublished - 2008 Aug 1
Externally publishedYes

Keywords

  • Cytokine
  • Gene expression
  • RNA-binding protein
  • STAT3
  • Signal transduction
  • Y14

ASJC Scopus subject areas

  • Biophysics
  • Biochemistry
  • Molecular Biology
  • Cell Biology

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