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Updated: Aug 19, 2026

Induction and Validation of Cellular Senescence in Primary Human Cells
Published on: June 20, 2018
Increased stability of the p16 mRNA with replicative senescence
Wengong Wang1, Jennifer L Martindale, Xiaoling Yang
1Laboratory of Cellular and Molecular Biology, National Institute on Aging-IRP, NIH, Baltimore, Maryland 21224, USA.
Abstract:
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.
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