Identification of Genes and microRNAs Associated with Midfacial Hypoplasia in Mice

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Authors: A. SUZUKI, Chihiro Iwaya, Ashley Jung, Ashley Huang, Junichi Iwata
Cited by: 0
References: 62

Abstract

Midfacial hypoplasia is a developmental defect caused by insufficient growth of the nasal placodes and maxillary prominences. While genetic studies in mice have identified key genes involved in midfacial development, the regulation of these genes during craniofacial development remains poorly understood. In this study, we demonstrate that microRNAs, short non-coding RNAs, play a crucial role in regulating genes involved in midfacial development. We identified 224 genes associated with midfacial malformations in mice. Through bioinformatics analyses, we predicted that several microRNAs, specifically miR-129-5p, miR-381-3p, miR-124-3p, miR-136-5p, miR-448-3p, miR-374, miR-96, and miR-882, could regulate the expression of these genes. Among these, we experimentally focused on the top four candidate microRNAs: miR-129-5p, miR-381-3p, miR-124-3p, and miR-136-5p. Our findings revealed that the overexpression of these microRNAs inhibited cell proliferation and osteogenesis in nasal process mesenchymal cells. These microRNAs regulated genes associated with midfacial malformations in a dose-dependent manner. Taken together, our results emphasize the significance of pathogenic microRNA-gene networks in the cause of midfacial malformations.

Fields of Study & Subjects

Cleft Lip and Palate Research Craniofacial Disorders and Treatments MicroRNA in disease regulation

Publication details

Journal / source
Cells
Volume
15
Issue
5
Pages
453–453
Publication date
3 March 2026
Language
EN