NF90 modulates processing of a subset of human pri-miRNAs. Issue 12 (19th May 2020)

• Record Type: Journal Article
• Authors: Grasso, Giuseppa; Higuchi, Takuma; Mac, Victor; Barbier, Jérôme; Helsmoortel, Marion; Lorenzi, Claudio; Sanchez, Gabriel; Bello, Maxime; Ritchie, William; Sakamoto, Shuji; Kiernan, Rosemary
• Is Part Of: Nucleic acids research. Volume 48:Issue 12(2020)
• Page Start: 6874
• Page End: 6888
• Publication Date: 2020-05-19
• Subjects: Nucleic acids -- Periodicals; Molecular biology -- Periodicals; 572.805
• DOI: 10.1093/nar/gkaa386
• Languages: English
• ISSNs: 0305-1048

Abstract

Abstract: MicroRNAs (miRNAs) are predicted to regulate the expression of >60% of mammalian genes and play fundamental roles in most biological processes. Deregulation of miRNA expression is a hallmark of most cancers and further investigation of mechanisms controlling miRNA biogenesis is needed. The double stranded RNA-binding protein, NF90 has been shown to act as a competitor of Microprocessor for a limited number of primary miRNAs (pri-miRNAs). Here, we show that NF90 has a more widespread effect on pri-miRNA biogenesis than previously thought. Genome-wide approaches revealed that NF90 is associated with the stem region of 38 pri-miRNAs, in a manner that is largely exclusive of Microprocessor. Following loss of NF90, 22 NF90-bound pri-miRNAs showed increased abundance of mature miRNA products. NF90-targeted pri-miRNAs are highly stable, having a lower free energy and fewer mismatches compared to all pri-miRNAs. Mutations leading to less stable structures reduced NF90 binding while increasing pri-miRNA stability led to acquisition of NF90 association, as determined by RNA electrophoretic mobility shift assay (EMSA). NF90-bound and downregulated pri-miRNAs are embedded in introns of host genes and expression of several host genes is concomitantly reduced. These data suggest that NF90 controls the processing of a subset of highly stable, intronic miRNAs.