Dicer loss and recovery induce an oncogenic switch driven by transcriptional activation of the oncofetal Imp1–3 family

• DOI: 10.1101/gad.296301.117
• Publication Date: 2017-04-26T18:10:28Z
• Authors: Courtney K. JnBap...; Allan M. Gurtan; Kevin K. Thai; Victoria Lu; Arjun Bhutkar; Mei-Ju Su; Asaf Rotem; Tyler Jacks; Phillip A. Sharp
• Keywords: Male; Mice, Knockout; Ribonuclease III; Transcriptional Activation; RNA-Binding Proteins; Oncogenes; 3. Good health; DEAD-box RNA Helicases; Gene Expression Regulation, Neoplastic; Mice; MicroRNAs; Cell Transformation, Neoplastic; Antigens, Neoplasm; Animals; Humans; Female; Cells, Cultured; Research Paper

MicroRNAs (miRNAs) are post-transcriptional regulators of gene expression critical for organismal viability. Changes in miRNA activity are common in cancer, but how these changes relate to subsequent alterations in transcription and the process of tumorigenesis is not well understood. Here, we report a deep transcriptional, oncogenic network regulated by miRNAs. We present analysis of the gene expression and phenotypic changes associated with global miRNA restoration in miRNA-deficient fibroblasts. This analysis uncovers a miRNA-repressed network containing oncofetal genes Imp1, Imp2, and Imp3 (Imp1–3) that is up-regulated primarily transcriptionally >100-fold upon Dicer loss and is resistant to resilencing by complete restoration of miRNA activity. This Dicer-resistant epigenetic switch confers tumorigenicity to these cells. Let-7 targets Imp1–3 are required for this tumorigenicity and feed back to reinforce and sustain expression of the oncogenic network. Together, these Dicer-resistant genes constitute an mRNA expression signature that is present in numerous human cancers and is associated with poor survival.