Bersani C, Xu L-D, Vilborg A, Lui W-O, Wiman K G
Cancer Center Karolinska (CCK), Department of Oncology-Pathology, Karolinska Institute, Stockholm, Sweden.
Oncogene. 2014 Aug 28;33(35):4407-17. doi: 10.1038/onc.2013.594. Epub 2014 Jan 27.
Wig-1, also known as ZMAT3, is a p53 target gene that encodes an RNA-binding zinc-finger protein involved in the regulation of mRNA stability through binding to AU-rich elements (AREs). We have used microarray analysis to identify novel Wig-1 target mRNAs. We identified 2447 transcripts with >fourfold differential expression between Wig-1 and control small interfering (si)RNA-treated HCT116 cells. Several p53 target genes were among the deregulated transcripts. We found that Wig-1 regulates FAS and 14-3-3σ mRNA independently of p53. We show that Wig-1 binds to FAS mRNA 3'-UTR and decreases its stability through an ARE in the 3'-UTR. Depletion of Wig-1 was associated with increased cell death and reduced cell cycle arrest upon DNA damage. Our results suggest a role of Wig-1 as a survival factor that directs the p53 stress response toward cell cycle arrest rather than apoptosis through the regulation of FAS and 14-3-3σ mRNA levels.
Wig-1,也称为ZMAT3,是一种p53靶基因,编码一种RNA结合锌指蛋白,该蛋白通过与富含AU元件(AREs)结合参与mRNA稳定性的调控。我们利用微阵列分析来鉴定新的Wig-1靶mRNA。我们在Wig-1和对照小干扰(si)RNA处理的HCT116细胞之间鉴定出2447个差异表达超过四倍的转录本。一些p53靶基因存在于失调的转录本中。我们发现Wig-1独立于p53调节FAS和14-3-3σ mRNA。我们表明Wig-1与FAS mRNA的3'-UTR结合,并通过3'-UTR中的一个ARE降低其稳定性。Wig-1的缺失与DNA损伤后细胞死亡增加和细胞周期阻滞减少有关。我们的结果表明Wig-1作为一种存活因子发挥作用,通过调节FAS和14-3-3σ mRNA水平,将p53应激反应导向细胞周期阻滞而非凋亡。