The MicroRNA, miR‐18a, Regulates NeuroD and Photoreceptor Differentiation in the Retina of Zebrafish

• Published in: Developmental neurobiology (Hoboken, N.J.) Vol. 79; no. 2; pp. 202 - 219
• Main Authors: Taylor, Scott M., Giuffre, Emily, Moseley, Patience, Hitchcock, Peter F.
• Format: Journal Article
• Language: English
• Published: United States Wiley Subscription Services, Inc 01.02.2019; John Wiley and Sons Inc
• Subjects: 3' Untranslated regions; Animals; Animals, Genetically Modified; Basic Helix-Loop-Helix Transcription Factors - genetics; Basic Helix-Loop-Helix Transcription Factors - metabolism; bHLH; Cell cycle; Cell Differentiation - genetics; Cell proliferation; Cell Proliferation - genetics; CRISPR; Danio rerio; Embryogenesis; Gene Expression Regulation, Developmental - genetics; Gene regulation; Genome editing; Helix-loop-helix proteins (basic); MicroRNAs; MicroRNAs - genetics; MicroRNAs - metabolism; miRNA; Nerve Tissue Proteins - metabolism; NeuroD protein; Neurogenesis; Neurogenesis - genetics; Oligonucleotides; Photoreceptors; post‐transcriptional; Retina; Retina - growth & development; retinal development; Transcription Factors - metabolism; Zebrafish - metabolism; photoreceptors; neurogenesis; miRNA; retinal development; post-transcriptional; bHLH
• ISSN: 1932-8451; 1932-846X; 1932-846X
• DOI: 10.1002/dneu.22666

During embryonic retinal development, six types of retinal neurons are generated from multipotent progenitors in a strict spatiotemporal pattern. This pattern requires cell cycle exit (i.e. neurogenesis) and differentiation to be precisely regulated in a lineage‐specific manner. In zebrafish, the bHLH transcription factor NeuroD governs photoreceptor genesis through Notch signaling but also governs photoreceptor differentiation though distinct mechanisms that are currently unknown. Also unknown are the mechanisms that regulate NeuroD and the spatiotemporal pattern of photoreceptor development. Members of the miR‐17‐92 microRNA cluster regulate CNS neurogenesis, and a member of this cluster, miR‐18a, is predicted to target neuroD mRNA. The purpose of this study was to determine if, in the developing zebrafish retina, miR‐18a regulates NeuroD and if it plays a role in photoreceptor development. Quantitative RT‐PCR showed that, of the three miR‐18 family members (miR‐18a, b, and c), miR‐18a expression most closely parallels neuroD expression. Morpholino oligonucleotides and CRISPR/Cas9 gene editing were used for miR‐18a loss‐of‐function (LOF) and both resulted in larvae with more mature photoreceptors at 70 hpf without affecting cell proliferation. Western blot showed that miR‐18a LOF increases NeuroD protein levels and in vitro dual luciferase assay showed that miR‐18a directly interacts with the 3′ UTR of neuroD. Finally, tgif1 mutants have increased miR‐18a expression, less NeuroD protein and fewer mature photoreceptors, and the photoreceptor deficiency is rescued by miR‐18a knockdown. Together, these results show that, independent of neurogenesis, miR‐18a regulates the timing of photoreceptor differentiation and indicate that this occurs through post‐transcriptional regulation of NeuroD.