Ashley-Koch A E, Robinson H, Glicksman A E, Nolin S L, Schwartz C E, Brown W T, Turner G, Sherman S L
Department of Genetics, Emory University School of Medicine, Atlanta, GA 30022, USA.
Am J Hum Genet. 1998 Sep;63(3):776-85. doi: 10.1086/302018.
We examined premutation-female transmissions and premutation-male transmissions of the FMR1 CGG repeat to carrier offspring, to identify factors associated with instability of the repeat. First we investigated associations between parental and offspring repeat size. Premutation-female repeat size was positively correlated with the risk of having full-mutation offspring, confirming previous reports. Similarly, premutation-male repeat size was positively correlated with the daughter's repeat size. However, increasing paternal repeat size was associated also with both increased risk of contraction and decreased magnitude of the repeat-size change passed to the daughter. We hypothesized that the difference between the female and male transmissions was due simply to selection against full-mutation sperm. To test this hypothesis, we simulated selection against full-mutation eggs, by only examining premutation-female transmissions to their premutation offspring. Among this subset of premutation-female transmissions, associations between maternal and offspring repeat size were similar to those observed in premutation-male transmissions. This suggests that the difference between female and male transmissions may be due to selection against full-mutation sperm. Increasing maternal age was associated with increasing risk of expansion to the full mutation, possibly because of selection for smaller alleles within the offspring's soma over time; a similar effect of increasing paternal age may be due to the same selection process. Last, we have evidence that the reported association between offspring sex and risk of expansion may be due to ascertainment bias. Thus, female and male offspring are equally likely to inherit the full mutation.
我们研究了FMR1基因CGG重复序列从携带前突变的女性和男性向其携带前突变的后代的传递情况,以确定与该重复序列不稳定性相关的因素。首先,我们调查了亲代与子代重复序列大小之间的关联。携带前突变的女性的重复序列大小与生出完全突变后代的风险呈正相关,这证实了之前的报道。同样,携带前突变的男性的重复序列大小与女儿的重复序列大小呈正相关。然而,父亲重复序列大小的增加还与收缩风险增加以及传递给女儿的重复序列大小变化幅度减小有关。我们推测,女性和男性传递情况的差异仅仅是由于对完全突变精子的选择。为了验证这一假设,我们通过只研究携带前突变的女性向其携带前突变后代的传递情况,模拟了对完全突变卵子的选择。在这一携带前突变的女性传递的子集中,母亲与后代重复序列大小之间的关联与在携带前突变的男性传递中观察到的相似。这表明女性和男性传递情况的差异可能是由于对完全突变精子的选择。母亲年龄增加与扩展至完全突变的风险增加有关,这可能是因为随着时间的推移,后代体细胞中较小等位基因受到了选择;父亲年龄增加产生的类似影响可能是由于相同的选择过程。最后,我们有证据表明,所报道的后代性别与扩展风险之间的关联可能是由于确诊偏倚。因此,女性和男性后代继承完全突变的可能性是相等的。