Genetic interactions between Pax9 and Msx1 regulate lip development and several stages of tooth morphogenesis
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Isolation and Time-Lapse Imaging of Primary Mouse Embryonic Palatal Mesenchyme Cells to Analyze Collective Movement Attributes
Published on: February 13, 2021
Mitsushiro Nakatomi1, Xiu-Ping Wang, Darren Key
1Institute of Human Genetics, Newcastle University, International Centre for Life, Central Parkway, Newcastle upon Tyne NE1 3BZ, UK.
Abstract:
Developmental abnormalities of craniofacial structures and teeth often occur sporadically and the underlying genetic defects are not well understood, in part due to unknown gene-gene interactions. Pax9 and Msx1 are co-expressed during craniofacial development, and mice that are single homozygous mutant for either gene exhibit cleft palate and an early arrest of tooth formation. Whereas in vitro assays have demonstrated that protein-protein interactions between Pax9 and Msx1 can occur, it is unclear if Pax9 and Msx1 interact genetically in vivo during development. To address this question, we compounded the Pax9 and Msx1 mutations and observed that double homozygous mutants exhibit an incompletely penetrant cleft lip phenotype. Moreover, in double heterozygous mutants, the lower incisors were consistently missing and we find that transgenic BMP4 expression partly rescues this phenotype. Reduced expression of Shh and Bmp2 indicates that a smaller "incisor field" forms in Pax9(+/-);Msx1(+/-) mutants, and dental epithelial growth is substantially reduced after the bud to cap stage transition. This defect is preceded by drastically reduced mesenchymal expression of Fgf3 and Fgf10, two genes that encode known stimulators of epithelial growth during odontogenesis. Consistent with this result, cell proliferation is reduced in both the dental epithelium and mesenchyme of double heterozygous mutants. Furthermore, the developing incisors lack mesenchymal Notch1 expression at the bud stage and exhibit abnormal ameloblast differentiation on both labial and lingual surfaces. Thus, Msx1 and Pax9 interact synergistically throughout lower incisor development and affect multiple signaling pathways that influence incisor size and symmetry. The data also suggest that a combined reduction of PAX9 and MSX1 gene dosage in humans may increase the risk for orofacial clefting and oligodontia.
Insights
Paired box 9 (Pax9) and Musculin (Msx1) genes interact genetically during craniofacial and tooth development. Their combined mutations in mice cause cleft lip and missing lower incisors, suggesting potential human risks for orofacial clefting and oligodontia.
Area of Science:
- Genetics
- Developmental Biology
- Craniofacial Development
Background:
- Developmental abnormalities in craniofacial structures and teeth are common but often lack clear genetic explanations.
- Paired box 9 (Pax9) and Musculin (Msx1) are key genes in craniofacial development, with single mutations causing cleft palate and arrested tooth formation.
- In vitro studies suggest Pax9 and Msx1 can interact, but their in vivo genetic interaction during development remains unclear.
Purpose of the Study:
- To investigate the in vivo genetic interaction between Pax9 and Msx1 during craniofacial and tooth development.
- To determine the consequences of combined Pax9 and Msx1 mutations on embryonic development and tooth formation.
- To elucidate the molecular mechanisms underlying the observed developmental defects.
Main Methods:
- Generation and analysis of double homozygous and double heterozygous mutant mice for Pax9 and Msx1.
- Phenotypic analysis including cleft palate, cleft lip, and tooth development assessment.
- Gene expression analysis (Shh, Bmp2, Fgf3, Fgf10, Notch1) and cell proliferation assays.
Main Results:
- Double homozygous mutants showed incompletely penetrant cleft lip.
- Double heterozygous mutants consistently lacked lower incisors, with partial rescue by transgenic BMP4.
- Reduced expression of Shh, Bmp2, Fgf3, and Fgf10, decreased cell proliferation, and abnormal Notch1 expression were observed in double heterozygotes.
- Abnormal ameloblast differentiation occurred in developing incisors of double heterozygotes.
Conclusions:
- Pax9 and Msx1 interact synergistically during lower incisor development, influencing tooth size and symmetry.
- The study identifies critical roles for Pax9 and Msx1 in signaling pathways regulating odontogenesis.
- Combined reduced dosage of PAX9 and MSX1 may increase human risk for orofacial clefting and oligodontia.
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