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Developmental constraint through negative pleiotropy in the zygomatic arch

机译:negative弓中负多效性的发展限制

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Background Previous analysis suggested that the relative contribution of individual bones to regional skull lengths differ between inbred mouse strains. If the negative correlation of adjacent bone lengths is associated with genetic variation in a heterogeneous population, it would be an example of negative pleiotropy, which occurs when a genetic factor leads to opposite effects in two phenotypes. Confirming negative pleiotropy and determining its basis may reveal important information about the maintenance of overall skull integration and developmental constraint on skull morphology. ResultsWe identified negative correlations between the lengths of the frontal and parietal bones in the midline cranial vault as well as the zygomatic bone and zygomatic process of the maxilla, which contribute to the zygomatic arch. Through gene association mapping of a large heterogeneous population of Diversity Outbred (DO) mice, we identified a quantitative trait locus on chromosome 17 driving the antagonistic contribution of these two zygomatic arch bones to total zygomatic arch length. Candidate genes in this region were identified and real-time PCR of the maxillary processes of DO founder strain embryos indicated differences in the RNA expression levels for two of the candidate genes, Camkmt and Six2 . ConclusionsA genomic region underlying negative pleiotropy of two zygomatic arch bones was identified, which provides a mechanism for antagonism in component bone lengths while constraining overall zygomatic arch length. This type of mechanism may have led to variation in the contribution of individual bones to the zygomatic arch noted across mammals. Given that similar genetic and developmental mechanisms may underlie negative correlations in other parts of the skull, these results provide an important step toward understanding the developmental basis of evolutionary variation and constraint in skull morphology.
机译:背景先前的分析表明,自交小鼠品系之间单个骨骼对区域头骨长度的相对贡献有所不同。如果相邻骨长度的负相关与异质群体中的遗传变异相关,则它将是负多效性的一个例子,当遗传因素导致两种表型产生相反的影响时,就会发生负性多效性。确认负多效性并确定其基础可能会揭示有关总体颅骨整合的维持和颅骨形态发育限制的重要信息。结果我们发现中线颅穹顶的额骨和顶骨的长度与上颌的骨和突之间呈负相关,这有助于the弓的形成。通过基因异种杂交多样性(DO)小鼠的大型异质种群的基因关联,我们确定了17号染色​​体上的定量性状基因座,驱动这两个弓足对总弓长度的拮抗作用。鉴定了该区域中的候选基因,DO建立者菌株胚胎上颌骨过程的实时PCR表明,两个候选基因Camkmt和Six2的RNA表达水平存在差异。结论确定了两个two骨弓负性多方性的潜在基因组区域,为拮抗总component弓长度提供了一种对抗组成骨长度的机制。这种机制可能导致单个骨骼对整个哺乳动物注意到的zy弓的贡献变化。鉴于相似的遗传和发育机制可能是颅骨其他部位负相关的基础,这些结果为理解颅骨形态进化变异和约束的发展基础提供了重要的一步。

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