ENU large-scale mutagenesis and quantitative trait linkage (QTL) analysis in mice: novel technologies for searching polygenetic determinants of craniofacial abnormalities.

Ichiro Nishimura, Thomas A Drake, Aldons J Lusis, Karen M Lyons, Joseph H Nadeau, Joseph Zernik
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引用次数: 15

Abstract

Discrepancies in size and shape of the jaws are the underlying etiology in many orthodontic and orthognathic surgery patients. Genetic factors combined with environmental interactions have been postulated to play a causal or contributory role in these craniofacial abnormalities. Along with the soon-to-be-available complete human and mouse genomic sequence data, mouse mutants have become a valuable tool in the functional mapping of genes involved in the development of human maxillofacial dysmorphologies. We review two powerful methods in such efforts: N-ethyl-N-nitrosourea (ENU) large-scale mutagenesis and quantitative trait linkage (QTL) analysis. The former aims at producing a plethora of novel variants of particular trait(s), and ultimately mapping the point mutations responsible for the appearance of these new traits. In contrast, the latter applies intensive breeding and mapping techniques to identify multiple loci (and, subsequently, genes) contributing to the phenotypic difference between the tested strains. A prerequisite for either approach to studying variations in the traits of interest is the application of effective mouse cephalometric phenotype analysis and rapid DNA mapping techniques. These approaches will produce a wealth of new data on critical genes that influence the size and shape of the human face.

小鼠ENU大规模突变和数量性状连锁(QTL)分析:寻找颅面异常多遗传决定因素的新技术。
颌骨大小和形状的差异是许多正畸和正颌手术患者的潜在病因。遗传因素结合环境相互作用被认为在这些颅面异常中起因果或促成作用。随着即将获得的完整的人类和小鼠基因组序列数据,小鼠突变体已成为人类颌面畸形发育相关基因功能定位的宝贵工具。本文综述了n -乙基-n -亚硝基脲(ENU)大规模诱变和数量性状连锁(QTL)分析两种有效方法。前者旨在产生特定性状的大量新变体,并最终绘制出导致这些新性状出现的点突变。相比之下,后者采用集约化育种和定位技术来鉴定导致被测菌株之间表型差异的多个位点(以及随后的基因)。任何一种方法研究感兴趣的性状变异的先决条件是有效的小鼠头测表型分析和快速DNA定位技术的应用。这些方法将产生大量关于影响人脸大小和形状的关键基因的新数据。
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