Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1996987 | Molecular Cell | 2012 | 12 Pages |
SummaryThe p53 tumor suppressor utilizes multiple mechanisms to selectively regulate its myriad target genes, which in turn mediate diverse cellular processes. Here, using conventional and single-molecule mRNA analyses, we demonstrate that the nucleoporin Nup98 is required for full expression of p21, a key effector of the p53 pathway, but not several other p53 target genes. Nup98 regulates p21 mRNA levels by a posttranscriptional mechanism in which a complex containing Nup98 and the p21 mRNA 3′UTR protects p21 mRNA from degradation by the exosome. An in silico approach revealed another p53 target (14-3-3σ) to be similarly regulated by Nup98. The expression of Nup98 is reduced in murine and human hepatocellular carcinomas (HCCs) and correlates with p21 expression in HCC patients. Our study elucidates a previously unrecognized function of wild-type Nup98 in regulating select p53 target genes that is distinct from the well-characterized oncogenic properties of Nup98 fusion proteins.
Graphical AbstractFigure optionsDownload full-size imageDownload high-quality image (233 K)Download as PowerPoint slideHighlights► Nup98 is required for full induction of select p53 target genes such as p21 ► Nup98 associates with the 3′UTR of p21 mRNA preventing exosomal degradation ► Nup98 is downregulated in murine and human HCC and correlates with p21 expression