Hallgrímsson Benedikt, Willmore Katherine, Dorval Curtis, Cooper David M L
Department of Cell Biology & Anatomy and the Joint Injury and Arthritis Research Group, University of Calgary, Calgary, Alberta T2N 4N1, Canada.
J Exp Zool B Mol Dev Evol. 2004 May 15;302(3):207-25. doi: 10.1002/jez.b.21002.
Evolutionary developmental biology of primates will be driven largely by the developmental biology of the house mouse. Inferences from how known developmental perturbations produce phenotypic effects in model organisms, such as mice, to how the same perturbations would affect craniofacial form in primates must be informed by comparisons of phenotypic variation and variability in mice and the primate species of interest. We use morphometric methods to compare patterns of cranial variability in homologous datasets obtained for two strains of laboratory mice and rhesus macaques. C57BL/6J represents a common genetic background for transgenic models. A/WySnJ mice exhibit altered facial morphology which results from reduction in the growth of the maxillary process during formation of the face. This is relevant to evolutionary changes in facial prognathism in nonhuman primate and human evolution. Rhesus macaques represent a nonhuman primate about which a great deal of phenotypic and genetic information is available. We find significant similarities in covariation patterns between the C57BL/6J mice and macaques. Among-trait variation in genetic and phenotypic variances are fairly concordant among the three groups, but among-trait variation in developmental stability is not. Finally, analysis of modularity based on phenotypic and genetic correlations did not reveal a consistent pattern in the three groups. We discuss the implications of these results for the study of evolutionary developmental biology of primates and outline a research strategy for integrating mouse genomics and developmental biology into this emerging field.
灵长类动物的进化发育生物学将在很大程度上由家鼠的发育生物学驱动。从已知的发育扰动如何在模型生物(如小鼠)中产生表型效应,推断这些相同的扰动如何影响灵长类动物的颅面形态,必须通过比较小鼠与感兴趣的灵长类物种的表型变异和变异性来进行。我们使用形态测量方法来比较从两种实验室小鼠品系和恒河猴获得的同源数据集中的颅骨变异性模式。C57BL/6J代表转基因模型的常见遗传背景。A/WySnJ小鼠表现出面部形态改变,这是由于面部形成过程中上颌突生长减少所致。这与非人类灵长类动物面部突颌的进化变化以及人类进化相关。恒河猴代表一种非人类灵长类动物,关于它有大量的表型和遗传信息可用。我们发现C57BL/6J小鼠和猕猴之间的协变模式存在显著相似性。三组之间遗传和表型方差的性状间变异相当一致,但发育稳定性的性状间变异并非如此。最后,基于表型和遗传相关性的模块性分析在三组中未揭示出一致的模式。我们讨论了这些结果对灵长类动物进化发育生物学研究的意义,并概述了将小鼠基因组学和发育生物学整合到这个新兴领域的研究策略。