*Department of Anatomy, Northeastern Ohio Universities Colleges of Medicine and Pharmacy, Rootstown, OH 44272, USA; Laboratory of Genetics, University of Wisconsin, Madison, WI 53706, USA.
Integr Comp Biol. 2008 Sep;48(3):324-37. doi: 10.1093/icb/icn063. Epub 2008 Jun 24.
The house mouse is one of the most successful mammals and the premier research animal in mammalian biology. The classical inbred strains of house mice have been artificially modified to facilitate identification of the genetic factors underlying phenotypic variation among these strains. Despite their widespread use in basic and biomedical research, functional and evolutionary morphologists have not taken full advantage of inbred mice as a model for studying the genetic architecture of form, function, and performance in mammals. We illustrate the potential of inbred mice as a model for mammalian functional morphology by examining the genetic architecture of maximum jaw-opening performance, or maximum gape, across 21 classical inbred strains. We find that variation in maximum gape among these strains is heritable, providing the first evidence of a genetic contribution to maximum jaw-opening performance in mammals. Maximum gape exhibits a significant genetic correlation with body size across strains, raising the possibility that evolutionary increases in size frequently resulted in correlated increases in maximum gape (within the constraints of existing craniofacial form) during mammalian evolution. Several craniofacial features that influence maximum gape share significant phenotypic and genetic correlations with jaw-opening ability across these inbred strains. The significant genetic correlations indicate the potential for coordinated evolution of craniofacial form and jaw-opening performance, as hypothesized in several comparative analyses of mammals linking skull form to variation in jaw-opening ability. Functional studies of mammalian locomotion and feeding have only rarely examined the genetic basis of functional and performance traits. The classical inbred strains of house mice offer a powerful tool for exploring this genetic architecture and furthering our understanding of how form, function, and performance have evolved in mammals.
家鼠是最成功的哺乳动物之一,也是哺乳动物生物学研究的主要实验动物。经典的近交系家鼠已经被人为地修改,以方便鉴定这些品系中表型变异的遗传因素。尽管它们在基础和生物医学研究中被广泛应用,但功能和进化形态学家并没有充分利用近交系小鼠作为研究形态、功能和性能遗传结构的模型来研究哺乳动物。我们通过研究 21 种经典近交系的最大张口性能(最大张口度)的遗传结构,说明了近交系小鼠作为哺乳动物功能形态学模型的潜力。我们发现,这些品系之间最大张口度的变异是可遗传的,这为哺乳动物最大张口性能的遗传贡献提供了第一个证据。最大张口度与品系间的体型大小有显著的遗传相关性,这表明在哺乳动物进化过程中,体型的进化增加经常导致最大张口度的相关增加(在现有颅面形态的限制内)。几个影响最大张口度的颅面特征与这些近交系的张口能力有显著的表型和遗传相关性。这些显著的遗传相关性表明,颅面形态和张口性能的协调进化具有潜力,正如在一些将头骨形态与张口能力变异联系起来的哺乳动物比较分析中所假设的那样。对哺乳动物运动和进食功能的研究很少涉及功能和性能特征的遗传基础。经典的近交系家鼠为探索这种遗传结构提供了一个有力的工具,并进一步加深了我们对形态、功能和性能如何在哺乳动物中进化的理解。