Van der Loos H, Welker E, Dörfl J, Rumo G
J Hered. 1986 Mar-Apr;77(2):66-82. doi: 10.1093/oxfordjournals.jhered.a110201.
The establishment of certain patterns of mystacial vibrissae in mice has been the aim of an extensive breeding program carried on in this laboratory since 1977. In a companion paper we have reported on variations in this pattern in an outbred population of ICR mice. Starting with 21 ICR animals we bred, mostly by brother-sister mating, for 13 bilaterally symmetric patterns of mystacial vibrissae characterized by the presence (or absence) of supernumerary whiskers (SWs). The strains are classified as follows: I, a mouse strain with the standard pattern; II, eight strains bred for the occurrence of SWs at a given site or sites; and III, four mouse strains bred for a maximal number of SWs in different regions of the whiskerpad. Commonly, SWs occur in regions that coincide with the zones of mergence between the three facial processes except for two class II strains in which we bred for SWs in the "straddler" row of vibrissae, and for one class III strain, in which we cultivated the tendency (that appeared late in our program) to have SWs at the crest of a facial process. For classes I and II we analyzed the results for about 18 generations in terms of "improvement," meaning an increase in the percentages of animals with the desired phenotype together with a decreased frequency of undesired SWs. For class III, success in breeding meant the increase of the mean number of the desired SWs. All results led to the same conclusion: there is a genetic basis for the occurrence of SWs. The side preference of a particular SW is not strain dependent. It disappears in those class I and II strains in which almost 100% of animals obtained the desired phenotype. The increase in number of SWs in one zone of mergence does not depend on the presence of SWs in the other. Where tested, we almost always found a representation of an SW in a topologically equivalent location within the "barrelfield" area of the somatosensory cerebral cortex. Except for some diseases early in the breeding program, and some side effects of inbreeding that were eliminated, the population was without obvious defects. Where tested, there was no correlation between the occurrence of SWs and sex. The observed variations in pattern of mystacial vibrissae and their genetic background led us to propose a morphogenetic model for the formation of the pattern of mystacial vibrissae.
自1977年以来,在本实验室开展的一项广泛育种计划的目标是培育出具有特定模式的小鼠触须。在一篇配套论文中,我们报道了ICR小鼠远交群体中这种模式的变异情况。我们从21只ICR动物开始,主要通过兄妹交配,培育出了13种双侧对称的触须模式,其特征是存在(或不存在)多余的触须(SWs)。这些品系分类如下:I型,具有标准模式的小鼠品系;II型,为在给定部位出现SWs而培育的8个品系;III型,为在触须垫不同区域获得最大数量的SWs而培育的4个小鼠品系。通常,SWs出现在与三个面部突起融合区域重合的部位,但有两个II型品系除外,在这两个品系中,我们培育出了在“跨骑”排触须中有SWs的小鼠,还有一个III型品系,我们培育出了(在我们的育种计划后期出现的)在面部突起顶部有SWs的倾向。对于I型和II型,我们根据“改进”情况分析了大约18代的结果,“改进”意味着具有所需表型的动物百分比增加,同时不需要的SWs频率降低。对于III型,育种成功意味着所需SWs的平均数量增加。所有结果都得出了相同的结论:SWs的出现有遗传基础。特定SW的侧向偏好不依赖于品系。在那些几乎100%的动物都获得所需表型的I型和II型品系中,这种偏好消失了。一个融合区域中SWs数量的增加不依赖于其他区域中SWs的存在。在进行测试的情况下,我们几乎总是在体感大脑皮层的“桶状区”内拓扑等效的位置发现SWs的表征。除了育种计划早期出现的一些疾病以及消除的近亲繁殖的一些副作用外,该群体没有明显缺陷。在进行测试的情况下,SWs的出现与性别之间没有相关性。观察到的触须模式变异及其遗传背景使我们提出了一个触须模式形成的形态发生模型。