An alternative miRISC targets a cancer-associated coding sequence mutation in FOXL2.
Eunkyoung ShinHanyong JinDae-Shik SuhYongyang LuoHye-Jeong HaTae Heon KimYongyang LuoSeogang HyunKangseok LeeJeehyeon BaePublished in: The EMBO journal (2020)
Recent evidence suggests that animal microRNAs (miRNAs) can target coding sequences (CDSs); however, the pathophysiological importance of such targeting remains unknown. Here, we show that a somatic heterozygous missense mutation (c.402C>G; p.C134W) in FOXL2, a feature shared by virtually all adult-type granulosa cell tumors (AGCTs), introduces a target site for miR-1236, which causes haploinsufficiency of the tumor-suppressor FOXL2. This miR-1236-mediated selective degradation of the variant FOXL2 mRNA is preferentially conducted by a distinct miRNA-loaded RNA-induced silencing complex (miRISC) directed by the Argonaute3 (AGO3) and DHX9 proteins. In both patients and a mouse model of AGCT, abundance of the inversely regulated variant FOXL2 with miR-1236 levels is highly correlated with malignant features of AGCT. Our study provides a molecular basis for understanding the conserved FOXL2 CDS mutation-mediated etiology of AGCT, revealing the existence of a previously unidentified mechanism of miRNA-targeting disease-associated mutations in the CDS by forming a non-canonical miRISC.
Keyphrases
- cell proliferation
- long non coding rna
- long noncoding rna
- mouse model
- cancer therapy
- end stage renal disease
- quantum dots
- transcription factor
- newly diagnosed
- drug delivery
- chronic kidney disease
- machine learning
- early onset
- single cell
- diabetic rats
- high glucose
- gene expression
- oxidative stress
- metabolic syndrome
- dna methylation
- deep learning
- autism spectrum disorder
- intellectual disability
- copy number
- genome wide
- patient reported outcomes
- endothelial cells
- polycystic ovary syndrome
- visible light
- young adults
- stress induced