Lamb N E, Feingold E, Sherman S L
Department of Genetics, Emory University, Atlanta, GA 30322, USA.
Am J Hum Genet. 1996 Jan;58(1):201-12.
Certain genetic disorders are rare in the general population but more common in individuals with specific trisomies, which suggests that the genes involved in the etiology of these disorders may be located on the trisomic chromosome. As with all aneuploid syndromes, however, a considerable degree of variation exists within each phenotype so that any given trait is present only among a subset of the trisomic population. We have previously presented a simple gene-dosage model to explain this phenotypic variation and developed a strategy to map genes for such traits. The mapping strategy does not depend on the simple model but works in theory under any model that predicts that affected individuals have an increased likelihood of disomic homozygosity at the trait locus. This paper explores the robustness of our mapping method by investigating what kinds of models give an expected increase in disomic homozygosity. We describe a number of basic statistical models for trisomic phenotypes. Some of these are logical extensions of standard models for disomic phenotypes, and some are more specific to trisomy. Where possible, we discuss genetic mechanisms applicable to each model. We investigate which models and which parameter values give an expected increase in disomic homozygosity in individuals with the trait. Finally, we determine the sample sizes required to identify the increased disomic homozygosity under each model. Most of the models we explore yield detectable increases in disomic homozygosity for some reasonable range of parameter values, usually corresponding to smaller trait frequencies. It therefore appears that our mapping method should be effective for a wide variety of moderately infrequent traits, even though the exact mode of inheritance is unlikely to be known.
某些遗传性疾病在普通人群中较为罕见,但在特定三体综合征患者中更为常见,这表明参与这些疾病病因的基因可能位于三体染色体上。然而,与所有非整倍体综合征一样,每个表型内部都存在相当程度的变异,因此任何给定的性状仅在三体人群的一个子集中出现。我们之前提出了一个简单的基因剂量模型来解释这种表型变异,并开发了一种定位此类性状基因的策略。该定位策略并不依赖于简单模型,而是在任何预测受影响个体在性状位点上二体纯合性增加可能性的模型下理论上都有效。本文通过研究哪些模型会导致二体纯合性预期增加来探讨我们定位方法的稳健性。我们描述了一些用于三体表型的基本统计模型。其中一些是二体表型标准模型的合理扩展,一些则更特定于三体。在可能的情况下,我们讨论适用于每个模型的遗传机制。我们研究哪些模型和哪些参数值会导致具有该性状的个体中二体纯合性预期增加。最后,我们确定在每个模型下识别增加的二体纯合性所需的样本量。我们探索的大多数模型在某些合理的参数值范围内会产生可检测到的二体纯合性增加,通常对应于较小的性状频率。因此,尽管确切的遗传模式不太可能已知,但我们的定位方法似乎对多种中度罕见的性状有效。