Khoury M J, Flanders W D, Beaty T H
Division of Chronic Disease Control, Centers for Disease Control, Atlanta, GA 30333.
Am J Med Genet. 1988 Feb;29(2):397-403. doi: 10.1002/ajmg.1320290222.
Many single-gene disorders (especially dominant traits) are known to exhibit "incomplete penetrance," a term often criticized as reflecting our ignorance of genetic and environmental factors that may interact with the genotype to determine the ultimate phenotype of the individual. We explore the effects of an environmental factor on penetrance for a simple model of single gene-mediated susceptibility to environmental factors. We show that penetrance of the susceptible genotype increases with increasing frequency of exposure to the factor and the strength of interaction between the factor and the genotype (relative risk). For disorders with disease frequency of 0.001 or less (as seen with many congenital malformations), penetrance is generally low (less than 10%) if the exposure frequency is low (less than 10%) even in the face of strong gene-environment interaction. Such low penetrance can lead to low recurrence risks. Single-gene effects could easily be overlooked in genetic analysis unless specific environmental factors are considered.
许多单基因疾病(尤其是显性性状)表现出“不完全外显”,这一术语常遭批评,因为它反映了我们对可能与基因型相互作用以决定个体最终表型的遗传和环境因素的无知。我们针对单基因介导的对环境因素易感性的简单模型,探讨一种环境因素对外显率的影响。我们表明,易感基因型的外显率会随着暴露于该因素的频率增加以及该因素与基因型之间的相互作用强度(相对风险)增加而升高。对于疾病频率为0.001或更低的疾病(如许多先天性畸形所见),即使存在强大的基因 - 环境相互作用,如果暴露频率较低(低于10%),外显率通常也较低(低于10%)。这种低外显率可能导致低复发风险。除非考虑特定的环境因素,单基因效应在遗传分析中很容易被忽视。