Vieland V J, Greenberg D A, Hodge S E
Columbia University, New York, NY.
Hum Hered. 1993 Nov-Dec;43(6):329-36. doi: 10.1159/000154155.
When a disease is controlled by two or more mendelian loci acting epistatically, it can be modeled in a linkage analysis as a single-locus mendelian disease with reduced penetrance. Previous work has demonstrated the reliability of such approximation for nuclear families, but not for extended pedigrees. We simulated extended pedigrees under two-locus models, in which one of the two disease loci was linked to a marker, and analyzed them both under the correct two-locus models and under single-locus approximations. The single-locus approximations provided results that were very close to the correct two-locus results. This held true, whether we ascertained pedigrees based on the presence of at least one affected individual, or based on the presence of at least five affected individuals. While a simulation study cannot guarantee that extrapolation of the results to models other than those examined is justified, our findings strongly suggest that single-locus linkage analysis can be reliably used in analyzing two-locus disorders in extended pedigrees. We also found striking confirmation of the importance of performing linkage analyses under both dominant and recessive models when the mode of inheritance is unknown, for extended pedigrees ascertained through multiple affected individuals.
当一种疾病由两个或更多上位性孟德尔位点控制时,在连锁分析中可将其模拟为具有降低外显率的单基因座孟德尔疾病。先前的研究已证明这种近似方法对核心家系是可靠的,但对扩展家系并非如此。我们在双基因座模型下模拟了扩展家系,其中两个疾病基因座之一与一个标记相连,并在正确的双基因座模型和单基因座近似模型下对其进行分析。单基因座近似法得出的结果与正确的双基因座结果非常接近。无论我们是基于至少有一个患病个体存在来确定家系,还是基于至少有五个患病个体存在来确定家系,都是如此。虽然模拟研究不能保证将结果外推到所研究模型之外的其他模型是合理的,但我们的研究结果强烈表明,单基因座连锁分析可可靠地用于分析扩展家系中的双基因座疾病。我们还显著证实了,当遗传模式未知时,对于通过多个患病个体确定的扩展家系,在显性和隐性模型下进行连锁分析的重要性。