Most cited article - PubMed ID 33235206
Ntrk1 mutation co-segregating with bipolar disorder and inherited kidney disease in a multiplex family causes defects in neuronal growth and depression-like behavior in mice
CDK13-related disorder, also known as congenital heart defects, dysmorphic facial features and intellectual developmental disorder (CHDFIDD) is associated with mutations in the CDK13 gene encoding transcription-regulating cyclin-dependent kinase 13 (CDK13). Here, we focused on the development of craniofacial structures and analyzed early embryonic stages in CHDFIDD mouse models, with one model comprising a hypomorphic mutation in Cdk13 and exhibiting cleft lip/palate, and another model comprising knockout of Cdk13, featuring a stronger phenotype including midfacial cleft. Cdk13 was found to be physiologically expressed at high levels in the mouse embryonic craniofacial structures, namely in the forebrain, nasal epithelium and maxillary mesenchyme. We also uncovered that Cdk13 deficiency leads to development of hypoplastic branches of the trigeminal nerve including the maxillary branch. Additionally, we detected significant changes in the expression levels of genes involved in neurogenesis (Ache, Dcx, Mef2c, Neurog1, Ntn1, Pou4f1) within the developing palatal shelves. These results, together with changes in the expression pattern of other key face-specific genes (Fgf8, Foxd1, Msx1, Meis2 and Shh) at early stages in Cdk13 mutant embryos, demonstrate a key role of CDK13 in the regulation of craniofacial morphogenesis.
- Keywords
- Axons, CDK13, Craniofacial development, Neurite outgrowth, Orofacial clefts, Trigeminal ganglion,
- MeSH
- Cyclin-Dependent Kinases metabolism genetics MeSH
- Embryo, Mammalian metabolism MeSH
- Embryonic Development * genetics MeSH
- Phenotype MeSH
- Skull embryology pathology MeSH
- Intellectual Disability genetics MeSH
- Disease Models, Animal * MeSH
- Mutation genetics MeSH
- Mice MeSH
- Trigeminal Nerve embryology MeSH
- Neurogenesis * genetics MeSH
- Face embryology abnormalities MeSH
- Doublecortin Protein MeSH
- Cleft Palate genetics pathology embryology MeSH
- Cleft Lip genetics pathology embryology MeSH
- Gene Expression Regulation, Developmental * MeSH
- Animals MeSH
- Check Tag
- Mice MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Cyclin-Dependent Kinases MeSH
- Dcx protein, mouse MeSH Browser
- Doublecortin Protein MeSH