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A landmark-free morphometrics pipeline for high-resolution phenotyping: application to a mouse model of Down syndrome.
Toussaint, Nicolas; Redhead, Yushi; Vidal-García, Marta; Lo Vercio, Lucas; Liu, Wei; Fisher, Elizabeth M C; Hallgrímsson, Benedikt; Tybulewicz, Victor L J; Schnabel, Julia A; Green, Jeremy B A.
Afiliação
  • Toussaint N; School of Biomedical Engineering and Imaging Sciences, King's College London, UK.
  • Redhead Y; Centre for Craniofacial Biology & Regeneration, King's College London, UK.
  • Vidal-García M; The Francis Crick Institute, London NW1 1AT, UK.
  • Lo Vercio L; Department of Cell Biology & Anatomy, University of Calgary, Calgary AB T2N 4N1, Canada.
  • Liu W; Department of Cell Biology & Anatomy, University of Calgary, Calgary AB T2N 4N1, Canada.
  • Fisher EMC; Department of Cell Biology & Anatomy, University of Calgary, Calgary AB T2N 4N1, Canada.
  • Hallgrímsson B; Department of Neurodegenerative Disease, Institute of Neurology, University College London, London WC1N 3BG, UK.
  • Tybulewicz VLJ; Department of Cell Biology & Anatomy, University of Calgary, Calgary AB T2N 4N1, Canada bhallgri@ucalgary.ca victor.t@crick.ac.uk jeremy.green@kcl.ac.uk.
  • Schnabel JA; The Francis Crick Institute, London NW1 1AT, UK bhallgri@ucalgary.ca victor.t@crick.ac.uk jeremy.green@kcl.ac.uk.
  • Green JBA; Department of Immunology & Inflammation, Imperial College London, London W12 0NN, UK.
Development ; 148(18)2021 03 12.
Article em En | MEDLINE | ID: mdl-33712441
ABSTRACT
Characterising phenotypes often requires quantification of anatomical shape. Quantitative shape comparison (morphometrics) traditionally uses manually located landmarks and is limited by landmark number and operator accuracy. Here, we apply a landmark-free method to characterise the craniofacial skeletal phenotype of the Dp1Tyb mouse model of Down syndrome and a population of the Diversity Outbred (DO) mouse model, comparing it with a landmark-based approach. We identified cranial dysmorphologies in Dp1Tyb mice, especially smaller size and brachycephaly (front-back shortening), homologous to the human phenotype. Shape variation in the DO mice was partly attributable to allometry (size-dependent shape variation) and sexual dimorphism. The landmark-free method performed as well as, or better than, the landmark-based method but was less labour-intensive, required less user training and, uniquely, enabled fine mapping of local differences as planar expansion or shrinkage. Its higher resolution pinpointed reductions in interior mid-snout structures and occipital bones in both the models that were not otherwise apparent. We propose that this landmark-free pipeline could make morphometrics widely accessible beyond its traditional niches in zoology and palaeontology, especially in characterising developmental mutant phenotypes.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Down / Imageamento Tridimensional / Pontos de Referência Anatômicos Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Development Assunto da revista: BIOLOGIA / EMBRIOLOGIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Reino Unido

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndrome de Down / Imageamento Tridimensional / Pontos de Referência Anatômicos Tipo de estudo: Prognostic_studies Limite: Animals Idioma: En Revista: Development Assunto da revista: BIOLOGIA / EMBRIOLOGIA Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Reino Unido