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唇腭裂易感性小鼠的颅面变异性与形态整合

Craniofacial variability and morphological integration in mice susceptible to cleft lip and palate.

作者信息

Hallgrímsson Benedikt, Dorval Curtis J, Zelditch Miriam Leah, German Rebecca Z

机构信息

Department of Cell Biology & Anatomy, the Joint Injury and Arthritis Research Group, University of Calgary, Canada.

出版信息

J Anat. 2004 Dec;205(6):501-17. doi: 10.1111/j.0021-8782.2004.00356.x.

Abstract

A/WySnJ mice are an inbred strain that develops cleft lip with or without cleft palate (CL/P) with a frequency of 25-30% and a predominantly unilateral expression pattern. As in humans, the pattern of incomplete penetrance, and variable and frequent unilateral expression suggests a role for altered regulation of variability (developmental stability, canalization and developmental integration) during growth. We compared both mean and variability parameters for craniofacial shape and size among A/WySnJ mice, a strain that does not develop CL/P (C57BL/6J) and their F1 cross. We show that adult A/WySnJ mice that do not express cleft lip exhibit decreased morphological integration of the cranium and that the co-ordination of overall shape and size variation is disrupted compared with both C57BL/6J mice and the F1 cross. The decrease in integration is most pronounced in the palate and face. The absence of this pattern in the F1 cross suggests that it is determined by recessive genetic factors. By contrast, the shape differences between the strains, which are thought to predispose A/WySnJ mice to CL/P, show a range of dominance which suggests a polygenic basis. We suggest that decreased integration of craniofacial growth may be an aetiological factor for CL/P in A/WySnJ mice.

摘要

A/WySnJ小鼠是一种近交系,会出现唇裂伴或不伴腭裂(CL/P),发生率为25%-30%,且主要为单侧表达模式。与人类一样,不完全外显率模式以及可变且频繁的单侧表达表明,生长过程中变异性调节(发育稳定性、发育稳态和发育整合)改变发挥了作用。我们比较了A/WySnJ小鼠、不发生CL/P的品系(C57BL/6J)及其F1杂交后代在颅面形状和大小方面的均值和变异性参数。我们发现未表现出唇裂的成年A/WySnJ小鼠颅部的形态整合性降低,与C57BL/6J小鼠和F1杂交后代相比,整体形状和大小变化的协调性受到破坏。整合性降低在腭部和面部最为明显。F1杂交后代中不存在这种模式,这表明它是由隐性遗传因素决定的。相比之下,品系之间的形状差异被认为是A/WySnJ小鼠易患CL/P的原因,呈现出一系列显性特征,这表明其具有多基因基础。我们认为颅面生长整合性降低可能是A/WySnJ小鼠CL/P的一个病因。

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