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Alternative polyadenylation confers Pten mRNAs stability and resistance to microRNAs.


ABSTRACT: Fine regulation of the phosphatase and tensin homologue (PTEN) phosphatase dosage is critical for homeostasis and tumour suppression. The 3'-untranslated region (3'-UTR) of Pten mRNA was extensively linked to post-transcriptional regulation by microRNAs (miRNAs). In spite of this critical regulatory role, alternative 3'-UTRs of Pten have not been systematically characterized. Here, we reveal an important diversity of Pten mRNA isoforms generated by alternative polyadenylation sites. Several 3'-UTRs are co-expressed and their relative expression is dynamically regulated. In spite of encoding multiple validated miRNA-binding sites, longer isoforms are largely refractory to miRNA-mediated silencing, are more stable and contribute to the bulk of PTEN protein and signalling functions. Taken together, our results warrant a mechanistic re-interpretation of the post-transcriptional mechanisms involving Pten mRNAs and raise concerns on how miRNA-binding sites are being validated.

SUBMITTER: Thivierge C 

PROVIDER: S-EPMC6212768 | biostudies-literature | 2018 Nov

REPOSITORIES: biostudies-literature

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Alternative polyadenylation confers Pten mRNAs stability and resistance to microRNAs.

Thivierge Caroline C   Tseng Hsin-Wei HW   Mayya Vinay K VK   Lussier Carine C   Gravel Simon-Pierre SP   Duchaine Thomas F TF  

Nucleic acids research 20181101 19


Fine regulation of the phosphatase and tensin homologue (PTEN) phosphatase dosage is critical for homeostasis and tumour suppression. The 3'-untranslated region (3'-UTR) of Pten mRNA was extensively linked to post-transcriptional regulation by microRNAs (miRNAs). In spite of this critical regulatory role, alternative 3'-UTRs of Pten have not been systematically characterized. Here, we reveal an important diversity of Pten mRNA isoforms generated by alternative polyadenylation sites. Several 3'-U  ...[more]

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