School of Biomedical Engineering and Imaging Sciences, King's College London, UK.
Centre for Craniofacial Biology & Regeneration, King's College London, UK.
Development. 2021 Mar 12;148(18):dev188631. doi: 10.1242/dev.188631.
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.
描述表型通常需要对解剖形状进行量化。传统的定量形状比较(形态测量学)使用手动定位的地标,并且受到地标数量和操作人员准确性的限制。在这里,我们应用无地标方法来描述唐氏综合征 Dp1Tyb 小鼠模型和多样性杂交(DO)小鼠模型的颅面骨骼表型,并将其与基于地标方法进行比较。我们确定了 Dp1Tyb 小鼠的颅面畸形,特别是较小的大小和短头畸形(前后缩短),与人类表型相似。DO 小鼠的形状变化部分归因于异速生长(与大小相关的形状变化)和性别二态性。无地标方法的表现与基于地标方法一样好,或者更好,但劳动强度更小,对用户的培训要求更低,并且独特地能够精细映射局部差异,例如平面扩展或收缩。其更高的分辨率指出了两个模型中内部鼻子中部结构和枕骨的减少,否则这些结构和枕骨是不明显的。我们提出,这种无地标流水线可以使形态测量学广泛应用于动物学和古生物学等传统领域之外,特别是在描述发育突变体表型方面。