Programa de Pós-Graduação em Genética e Biologia Molecular, Universidade Federal do Rio Grande do Sul, Porto Alegre, Brazil.
Serviço de Neurologia, Hospital de Clínicas de Porto Alegre, Porto Alegre, Brazil.
Cerebellum. 2019 Apr;18(2):188-194. doi: 10.1007/s12311-018-0977-7.
Spinocerebellar ataxia type 2 (SCA2) is caused by an unstable expanded CAG repeat tract (CAGexp) at ATXN2. Although prone to selective forces such as anticipation, SCA2 frequency seems to be stable in populations. Our aim was to estimate reproductive success, segregation patterns, and role of anticipation in SCA2. Adult subjects from families with molecular diagnosis provided data about all his/her relatives. Affected and unaffected sibs older than 65.7 years of age were used to estimate reproductive success and segregation patterns. Twenty-one SCA2 families were studied, including 1017 individuals (164 affected) who were born from 1840 to 2012. The median number of children of the non-carriers and carriers, among 99 subjects included in the reproductive success analysis, were 2 and 3 (p < 0.025), respectively. Therefore, the reproductive success of carriers was 1.5. There were 137 non-carriers (59.6%) and 93 carriers (40.4%) (p = 0.04), among subjects included in the segregation analysis. Age at onset across generations pointed to anticipation as a frequent phenomenon. We raised evidence in favor of increased reproductive success related to the carrier state at ATXN2, and segregation distortion favoring normal alleles. Since majority of normal alleles analyzed carried 22 repeats, we propose that this distortion segregation can be related to the high frequency of this allele in human chromosomes.
脊髓小脑性共济失调 2 型(SCA2)是由 ATXN2 上不稳定的 CAG 重复序列(CAGexp)引起的。尽管易受选择压力(如预期)的影响,但 SCA2 的频率在人群中似乎是稳定的。我们的目的是估计生殖成功、分离模式以及预期在 SCA2 中的作用。有分子诊断的家庭的成年受试者提供了有关其所有亲属的信息。年龄大于 65.7 岁的受影响和未受影响的兄弟姐妹用于估计生殖成功和分离模式。研究了 21 个 SCA2 家系,包括 1840 年至 2012 年出生的 1017 个人(164 名受影响者)。在生殖成功分析中包括的 99 名受试者中,非携带者和携带者的中位数子女数分别为 2 和 3(p < 0.025)。因此,携带者的生殖成功率为 1.5。在包括在分离分析中的受试者中,有 137 名非携带者(59.6%)和 93 名携带者(40.4%)(p = 0.04)。代际发病年龄表明预期是一种常见现象。我们提出了支持与 ATXN2 携带者状态相关的生殖成功增加和有利于正常等位基因的分离失真的证据。由于分析的大多数正常等位基因携带 22 个重复序列,我们提出这种分离失真可能与人类染色体中该等位基因的高频有关。