Bauer P O, Zumrova A, Matoska V, Marikova T, Krilova S, Boday A, Singh B, Goetz P
Neurogenetic Centre of the Institute of Biology and Medical Genetics, Department of Child Neurology, 2nd Medical Faculty of Charles University and Faculty Hospital Motol, Prague, Czech Republic.
Eur J Neurol. 2005 Nov;12(11):851-7. doi: 10.1111/j.1468-1331.2005.01090.x.
Although spinocerebellar ataxia type 3 (SCA3)/Machado-Joseph disease is the most common type of SCA worldwide, we did not identify any cases of the disease amongst SCA patients in the Czech population. It has been proposed that the prevalence of large normal alleles correlates with the frequency of various types of SCA. We have therefore attempted to resolve the absence of SCA3 in our population by investigating, within 204 normal chromosomes, the frequency and nature of CAG repeats as well as two intragenic polymorphisms. We found that large normal alleles with more than 33 CAG repeats were observed at a frequency of only 0.49%. Whereas most of the expanded alleles worldwide have the CA haplotype, this was the least common (5.4%) variant observed in our study, although it was associated with a larger mean CAG repeat length (26.9). We postulate that the absence of SCA3 in the Czech population might be explained by the lack of large normal alleles and consequently a relatively small reservoir for aberrant CAG expansions at the SCA3 locus.
尽管3型脊髓小脑共济失调(SCA3)/马查多-约瑟夫病是全球最常见的SCA类型,但我们在捷克人群的SCA患者中未发现任何该疾病的病例。有人提出,大的正常等位基因的流行率与各种类型SCA的频率相关。因此,我们试图通过在204条正常染色体中研究CAG重复序列的频率和性质以及两个基因内多态性,来解释我们人群中SCA3的缺失情况。我们发现,CAG重复序列超过33个的大正常等位基因的出现频率仅为0.49%。虽然全球大多数扩增等位基因具有CA单倍型,但这是我们研究中观察到的最不常见(5.4%)的变体,尽管它与较大的平均CAG重复长度(26.9)相关。我们推测,捷克人群中SCA3的缺失可能是由于缺乏大的正常等位基因,因此SCA3位点异常CAG扩增的储备相对较小。