Increased stability of the p16 mRNA with replicative senescence

被引:77
作者
Wang, WG
Martindale, JL
Yang, XL
Chrest, FJ
Gorospe, M [1 ]
机构
[1] NIA, Cellular & Mol Biol Lab, IRP, NIH, Baltimore, MD 21224 USA
[2] NIA, Res Resources Branch, IRP, NIH, Baltimore, MD 21224 USA
关键词
INK4a; mRNA turnover; AUF1; post-transcriptional regulation;
D O I
10.1038/sj.embor.7400346
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Expression of p16(INK4a) is elevated during ageing and replicative senescence. Here, we report the presence of an instability determinant within the 3'-untranslated region (UTR) of the p16 messenger RNA in WI-38 human diploid fibroblasts. The p16 3'UTR was found to be a specific target of AUF1, an RNA-binding protein implicated in promoting mRNA decay. Both AUF1 levels and AUF1-p16 mRNA associations were strikingly more abundant in early-passage than late-passage fibroblast cultures. Moreover, short interfering RNA-based reductions in AUF1 levels increased the stability of p16 3'UTR-containing transcripts, elevated the expression of p16 and accentuated the senescence phenotype. Together, our findings show that p16 mRNA turnover decreases during replicative senescence and that the instability-conferring region is located within the 3'UTR of p16, as well as identifying AUF1 as a critical mediator of these regulatory events.
引用
收藏
页码:158 / 164
页数:7
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