Haploinsufficiency of the miR-873/miR-876 microRNA cluster is associated with craniofacial abnormalities
2015
Koufaris, Costas | Papagregoriou, Gregoris | Kousoulidou, Ludmila | Moutafi, Maria | Tauber, Maïthé | Jouret, Béatrice | Kieffer, Isabelle | Deltas, Constantinos | Tanteles, George A. | Anastasiadou, Violetta | Patsalis, Philippos C. | Sismani, Carolina
MicroRNA haploinsufficiency has been associated with developmental defects in only a limited number of cases. Here we report a de novo genomic microdeletion that includes the LINGO2 gene as well as two microRNA genes, MIR873 and MIR876, in a patient with craniofacial abnormalities — in particular macrocephaly and hypertelorism — and learning difficulties. Subsequent analysis revealed that the microRNAs affected by this de novo microdeletion form a mammalian-lineage, neuronal tissue-enriched cluster. In addition, bioinformatic analysis and experimental data indicate that miR-873 is involved in the regulation of the Hedgehog signaling, an essential pathway involved in craniofacial patterning and differentiation. Collectively these observations are consistent with a role of the miR-873/miR-876 microRNA cluster in physiological cranial bone development and indicate that mutations affecting these microRNAs could be a rare cause of developmental defect in humans.
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