Dizier M H, Babron M C, Clerget-Darpoux F
Unité de Recherches d'Epidemiologie Génétique INSERM, Unité 155, Laboratoire d'Anthropologie Biologique, Université Paris 7, France.
Am J Hum Genet. 1994 Nov;55(5):1042-9.
For elucidating the genetic component of multifactorial diseases, it is important to investigate the effect of several factors and the possible interaction between them. In particular, for many diseases it is interesting to study the interactive effect of two genes. In this context, the marker-association-segregation chi 2 method (MASC), initially proposed to detect the involvement of a candidate gene in multifactorial diseases, is developed here to investigate the involvement of two candidate genes and to model the joint effect of these two genes. In particular, it is possible to precisely determine whether the joint effect of both genes is multiplicative. This extension simultaneously uses information on two markers, one for each candidate gene, at both the population and the familial segregation level. We show here that there can be an important gai of power to detect the effect of a second gene in a disease when information is used simultaneously on two markers instead of studying each marker separately. This extension of MASC is then applied on a sample of insulin-dependent diabetes (IDD) families typed for the markers of two candidate regions: HLA and that of the insulin gene (INS). This analysis allows us to confirm the involvement of INS in IDD, and the best-fitting model is a multiplicative (noninteractive) effect of HLA and INS, with a biallelic locus for INS and a complementation model for HLA.
为阐明多因素疾病的遗传成分,研究多种因素的作用及其间可能的相互作用非常重要。特别地,对于许多疾病而言,研究两个基因的交互作用很有意思。在此背景下,最初提出用于检测候选基因与多因素疾病相关性的标记 - 关联 - 分离卡方方法(MASC)在此得到拓展,以研究两个候选基因的相关性并对这两个基因的联合效应进行建模。具体而言,能够精确确定两个基因的联合效应是否为相乘性的。这种拓展同时在群体和家系分离水平上利用了两个标记的信息,每个候选基因对应一个标记。我们在此表明,当同时使用两个标记的信息而非分别研究每个标记时,检测疾病中第二个基因效应的效能可能会有显著提高。然后将这种MASC的拓展应用于一个胰岛素依赖型糖尿病(IDD)家系样本,这些家系针对两个候选区域的标记进行了分型:HLA和胰岛素基因(INS)的标记。该分析使我们能够确认INS与IDD有关,并且最佳拟合模型是HLA和INS的相乘性(非交互性)效应,INS为双等位基因位点,HLA为互补模型。