Year: 2017
Type: article
Abstract: MicroRNAs (miRNAs) are important regulators of diverse physiological and pathophysiological processes. MiRNA families and clusters are two key features in miRNA biology. Here we explore the use of CRISPR/Cas9 as a powerful tool to delineate the function and regulation of miRNA families and clusters. We focused on four miRNA clusters composed of miRNA members of the same family, homo-clusters or different families, hetero-clusters. Our results highlight different regulatory mechanisms in miRNA cluster expression. In the case of the miR-497~195 cluster, editing of miR-195 led to a significant decrease in the expression of the other miRNA in the cluster, miR-497a. Although no gene editing was detected in the miR-497a genomic locus, computational simulation revealed alteration in the three dimensional structure of the pri-miR-497~195 that may affect its processing. In cluster miR-143~145 our results imply a feed-forward regulation, although structural changes cannot be ruled out. Furthermore, in the miR-17~92 and miR-106~25 clusters no interdependency in miRNA expression was observed. Our findings suggest that CRISPR/Cas9 is a powerful gene editing tool that can uncover novel mechanisms of clustered miRNA regulation and function.
Source: Scientific Reports
Language: English
Subfield: Cancer Research
Domain: Life Sciences
Open Access status: gold
Estimated APC paid: $2,690
Awards: Zinc finger nuclease-induced homologous recombination in zebrafish., Zinc finger nuclease-induced homologous recombination in zebrafish., G2947176565, Proteomics to explore mechanistic links between circulating MiRNAs and response to vascular injury, Mechanisms of activity-dependent muscle growth and repair, G4582407259, The BHF Chair of Cardiovascular Proteomics, Exploring known and novel biomarkers of cardiovascular disease, The novel role of miR-15 family in extracellular matrix remodelling in the vasculature, Circulating microRNAs as novel biomarkers for cardiovascular risk, G920601303
OpenAlex ID: W2742734776
