Feingold J
Unité de recherches d'épidémiologie génétique, Inserm U155, université Paris-VII, France.
C R Acad Sci III. 1998 Jul;321(7):553-5. doi: 10.1016/s0764-4469(98)80456-3.
Hereditary diseases have been reported with relatively high frequency in some small populations. Founder effect and genetic drift, associated or not with selective advantage of heterozygotes in case of recessive diseases, are the main explanations. Therefore, if we consider one population and one particular disease, only one deleterious allele should be observed. Determination of mutations has shown that in most cases the situation is more complex; more than one mutation is found among the patients. This finding can be explained by a multiple founder effect, with genetic drift and new mutations.
在一些小群体中,遗传性疾病的报道频率相对较高。奠基者效应和遗传漂变是主要的解释因素,在隐性疾病中,它们可能与杂合子的选择优势有关,也可能无关。因此,如果我们考虑一个群体和一种特定疾病,理论上应该只观察到一个有害等位基因。然而,突变检测表明,在大多数情况下,情况更为复杂;在患者中发现了不止一种突变。这一发现可以用多重奠基者效应、遗传漂变和新突变来解释。