| Literature DB >> 25680557 |
Costas Koufaris1, Gregoris Papagregoriou2, Ludmila Kousoulidou1, Maria Moutafi1, Maithé Tauber3, Béatrice Jouret3, Isabelle Kieffer4, Constantinos Deltas2, George A Tanteles5, Violetta Anastasiadou6, Philippos C Patsalis7, Carolina Sismani8.
Abstract
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.Entities:
Keywords: Craniofacial; Developmental defect; Haploinsufficiency; Hedgehog; miR-873; miR-876
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Year: 2015 PMID: 25680557 DOI: 10.1016/j.gene.2015.02.018
Source DB: PubMed Journal: Gene ISSN: 0378-1119 Impact factor: 3.688