Naofen, a novel WD40-repeat protein, mediates spontaneous and tumor necrosis factor-induced apoptosis

  • Guo Gang Feng
  • , Chang Li
  • , Lei Huang
  • , Koji Tsunekawa
  • , Yuko Sato
  • , Yoshihiro Fujiwara
  • , Tooru Komatsu
  • , Takashi Honda
  • , Jun Hua Fan
  • , Hidemi Goto
  • , Tatsuro Koide
  • , Takaaki Hasegawa
  • , Naohisa Ishikawa

Research output: Contribution to journalArticlepeer-review

Abstract

Naofen has recently been identified from the rat brain/spinal cord cDNA library as a substance reactive against an anti-shigatoxin (Stx)-2 antibody. Naofen mRNA is composed of 4620 nucleotides and encodes 1170 amino acids. Naofen contains four WD-repeat domains in its N-terminus and is ubiquitously distributed in many tissues of the rat. Tumor necrosis factor (TNF)-α enhanced the expression of naofen mRNA in HEK293 cells in a dose-dependent manner. Furthermore, naofen siRNA, which predominantly knocked down the expression of naofen mRNA, significantly reduced both TNF-α-induced caspase-3 activation and apoptosis in HEK293 cells. Overexpression of naofen in HEK293 cells (FLAG-NF) spontaneously induced caspase -3 activation and apoptosis, and showed extremely high susceptibility to TNF-α-induced apoptosis. These results indicated that naofen may function as a novel modulator activating caspase-3, and promoting TNF-α-stimulated apoptosis.

Original languageEnglish
Pages (from-to)153-157
Number of pages5
JournalBiochemical and Biophysical Research Communications
Volume394
Issue number1
DOIs
Publication statusPublished - 26-03-2010
Externally publishedYes

All Science Journal Classification (ASJC) codes

  • Biophysics
  • Biochemistry
  • Molecular Biology
  • Cell Biology

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