Lymbery A J
Western Australian Department of Agriculture, Bunbury, Australia.
Int J Parasitol. 1996 Jan;26(1):7-17. doi: 10.1016/0020-7519(95)00109-3.
The identification, mapping and eventual cloning of genes which determine or influence important epidemiological traits in parasites can have great benefits for the control of parasitic disease. In this review, strategies are outlined for identifying genetic markers for complex, quantitative traits. A genetic marker is a variable DNA sequence which co-occurs with a variable quantitative trait. Candidate markers are chosen because they are thought to directly influence the trait whereas random markers are expected to be linked to another DNA sequence which influences the trait. Association studies compare the value of a quantitative trait between different marker genotype classes in a population, without regard to family structure. Linkage studies compare the value of a quantitative trait between marker genotype classes within families or within a population (usually derived from a cross between inbred lines) which is segregating for both marker and quantitative trait loci. The most commonly used analytical methods for determining the significance of association or linkage between marker and quantitative trait loci, and for estimating parameters such as recombination rate and quantitative gene action, are least-squares and maximum likelihood. Both methods may be used to test either single markers or the interval between flanking markers, and both suffer from the need to minimize type I and type II error rates with multiple tests.
鉴定、定位并最终克隆那些决定或影响寄生虫重要流行病学特征的基因,对于控制寄生虫病可能具有极大的益处。在本综述中,概述了用于鉴定复杂数量性状遗传标记的策略。遗传标记是一种与可变数量性状同时出现的可变DNA序列。选择候选标记是因为它们被认为直接影响该性状,而随机标记预计与另一个影响该性状的DNA序列连锁。关联研究比较群体中不同标记基因型类别的数量性状值,而不考虑家系结构。连锁研究比较家系内或群体内(通常来自近交系之间的杂交)标记基因型类别的数量性状值,该群体中标记和数量性状位点均发生分离。用于确定标记与数量性状位点之间关联或连锁的显著性,以及估计诸如重组率和数量基因作用等参数的最常用分析方法是最小二乘法和最大似然法。这两种方法都可用于测试单个标记或侧翼标记之间的区间,并且都面临着在多次测试中需要将I型和II型错误率降至最低的问题。