Grewal R P, Cancel G, Leeflang E P, Dürr A, McPeek M S, Draghinas D, Yao X, Stevanin G, Alnot M O, Brice A, Arnheim N
Program in Molecular Biology, SHS 172, 835 West 37th Street, University of Southern California, Los Angeles, CA 90089-1340, USA.
Hum Mol Genet. 1999 Sep;8(9):1779-84. doi: 10.1093/hmg/8.9.1779.
Segregation distortion has been reported to occur in a number of the trinucleotide repeat disorders. On the basis of a sperm typing study performed in patients of Japanese descent with Machado-Joseph disease (MJD), it was reported that disease alleles are preferentially transmitted during meiosis. We performed a sperm typing study of five MJD patients of French descent and analysis of the pooled data shows a ratio of mutant to normal alleles of 379:436 (46.5:53.5%), which does not support meiotic segregation distortion. To confirm these results, sperm typing analysis was also performed using a polymorphic marker, D14S1050, closely linked to the MJD1 gene. Among 910 sperm analyzed, the allele linked to the disease chromosome was detected in 50.3% of the samples and the allele linked to the normal chromosome was found in 49.6% of the sperm. The difference in frequency of these two alleles is not significant ( P = 0.8423). Likelihood-based analysis of segregation distortion in the single sperm data using the SPERMSEG program also showed no support for segregation distortion at the gamete level in this patient population. The previous report on the Japanese patients also suggested that disease allele stability may be influenced by a trans effect of an intragenic polymorphism (987 G/C) in the wild-type allele. All of the French patients were heterozygous for this polymorphism. However, analysis of the variance in repeat number in sperm from the French MJD patients overlapped significantly with the variance in repeat number observed in the C/C homozygous Japanese patients.
据报道,在一些三核苷酸重复序列疾病中会发生分离畸变。基于对日本裔马查多-约瑟夫病(MJD)患者进行的精子分型研究,有报道称疾病等位基因在减数分裂期间优先传递。我们对五名法国裔MJD患者进行了精子分型研究,汇总数据分析显示突变等位基因与正常等位基因的比例为379:436(46.5:53.5%),这并不支持减数分裂分离畸变。为了证实这些结果,还使用与MJD1基因紧密连锁的多态性标记D14S1050进行了精子分型分析。在分析的910个精子中,与疾病染色体相关的等位基因在50.3%的样本中被检测到,与正常染色体相关的等位基因在49.6%的精子中被发现。这两个等位基因频率的差异不显著(P = 0.8423)。使用SPERMSEG程序对单个精子数据中的分离畸变进行基于似然性的分析也表明,在该患者群体的配子水平上不支持分离畸变。之前关于日本患者的报告还表明,疾病等位基因稳定性可能受野生型等位基因中基因内多态性(987 G/C)的反式效应影响。所有法国患者在该多态性上均为杂合子。然而,对法国MJD患者精子中重复数目的方差分析与在C/C纯合日本患者中观察到的重复数目的方差有显著重叠。