Publications [#363682] of Megan A. Holmes

Journal Articles

1. Ogg, ML; Pennings, AN; McNulty, MA; Holmes, MA; Mussell, JC; DeLeon, VB, Increased Integration in Mutant Mice: An Analysis of the Patterns of Covariance through Ontogeny in Fgfr2 Mice, FASEB journal : official publication of the Federation of American Societies for Experimental Biology, vol. 36 (May, 2022) [doi]
   (last updated on 2024/04/24)

   Abstract:
   Mutations in the FGF/FGFR2 gene result in the premature fusion of fibrous and cartilaginous joints in the skull. This results in profound morphological changes in the skulls of both humans and mice with these mutations. Previous studies have indicated that morphological integration of the skull is expected to become more pronounced in dysmorphic syndromes, including FGFR2 syndromes which result in craniosynostosis. In this study, our objective was to test two hypotheses: 1) that the magnitude of morphological integration was greater in Fgfr2C342Y/+ mutant mice relative to wild-type littermates; and 2) that the magnitude of morphological integration would increase through ontogeny. Our sample included Fgfr2C342Y/+ mutants and wild-type littermates at postnatal day 14 (P14) and adult stages. We used micro-computed tomography (microCT) scans to create image volumes of the skull. Virtual reconstructions of the cranium were produced in 3DSlicer software, using volume renders based on tissue densities to define the surface of the bone. We collected coordinate data for 38 biologically homologous landmarks with approximately equal distribution across face and neurocranium. All morphometric analyses were conducted using the geomorph package in R. The sample was subdivided by Age and Genotype. Landmark coordinates were divided into face and neurocranium modules. Coordinate data for each subset were superimposed with object symmetry using the bilat.symmetry() function. Covariance across modules was tested using the two.b.pls() function for each sample subset. Results confirmed our expectation that the magnitude of covariation between face and neurocranium increased in the mutant sample relative to the wild-type sample at both timepoints. Surprisingly, within the mutant sample, integration between face and neurocranium was greater in the younger P14 mice than the older adults. Results of this study can be used to inform researchers about patterns of covariance that can be applied to better understand craniosynostosis syndromes that affect humans.