Alternative Polyadenylation Orchestrates Dynamic Gene Regulation of Endogenous dsRNAs

Abstract

Alu elements are the most abundant type of SINE and consist over 10% of the human genome. Inverted repeats of Alu elements (IRAlus) in 3' UTR can form intramolecular double-stranded RNAs (dsRNAs) which affect the subcellular localization and translation of the host mRNA. However, the transcriptome-wide regulatory potential of these IRAlus elements remains largely unknown. Here, we utilized various database to identify genes that contain functional IRAlus elements in 3' UTR at the transcriptome level. We find that mRNAs with proximal IRAlus elements compared to polyadenylation sites (n = 259) show increased nuclear retention and decreased translation efficiency while distal IRAlus-containing mRNAs (n = 353) are indistinguishable from those of non-IRAlus mRNAs. Moreover, our analysis of J2 fCLIP-sequencing identifies 797 transcripts that may contain IRAlus elements in their 3' UTR. We further find that the gene regulation by the IRAlus element is determined by the polyadenylation factors. In particular, we show that p53 pathway can be activated via lengthening of 3' UTR of MDM2 and subsequent inclusion of the IRAlus element. Our work unveils the dynamic regulation of IRAlus-mediated gene silencing through alternative polyadenylation sites and suggests dsRNA structure as a regulator of numerous biological processes including ubiquitination.