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PUMILIO competes with AUF1 to control DICER1 RNA levels and miRNA processing.

Swetha RajasekaranEshan KhanSamuel R ChingMisbah KhanJalal K SiddiquiDaniela F GradiaChenyu LinStephanie J BouleyDayna L MercadanteAmity L ManningAndré P GerberJames A WalkerWayne O Miles
Published in: Nucleic acids research (2022)
DICER1 syndrome is a cancer pre-disposition disorder caused by mutations that disrupt the function of DICER1 in miRNA processing. Studying the molecular, cellular and oncogenic effects of these mutations can reveal novel mechanisms that control cell homeostasis and tumor biology. Here, we conduct the first analysis of pathogenic DICER1 syndrome allele from the DICER1 3'UTR. We find that the DICER1 syndrome allele, rs1252940486, abolishes interaction with the PUMILIO RNA binding protein with the DICER1 3'UTR, resulting in the degradation of the DICER1 mRNA by AUF1. This single mutational event leads to diminished DICER1 mRNA and protein levels, and widespread reprogramming of miRNA networks. The in-depth characterization of the rs1252940486 DICER1 allele, reveals important post-transcriptional regulatory events that control DICER1 levels.
Keyphrases
  • binding protein
  • single cell
  • stem cells
  • gene expression
  • squamous cell carcinoma
  • mesenchymal stem cells
  • oxidative stress
  • young adults
  • single molecule
  • genome wide
  • cell therapy
  • amino acid