Sherman S L, Petersen M B, Freeman S B, Hersey J, Pettay D, Taft L, Frantzen M, Mikkelsen M, Hassold T J
Department of Genetics and Molecular Medicine, Emory University School of Medicine, Atlanta, GA 30322.
Hum Mol Genet. 1994 Sep;3(9):1529-35. doi: 10.1093/hmg/3.9.1529.
Over 300 cases of trisomy 21 were analyzed to characterize the causes of maternal non-disjunction and to evaluate the basis for maternal age-dependent trisomy 21. We confirmed the observation that recombination along 21q is reduced among non-disjoined chromosomes 21 and further demonstrated that the alterations in recombination are restricted to meiosis I origin. Analysis of the crossover distribution indicates that reduction in recombination is not due simply to failure of pairing and/or absence of recombination in a proportion of cases. Instead, we observed an increase in both zero- and one-exchange events among trisomy 21-generating meioses suggesting that an overall reduction in recombination may be the underlying cause of non-disjunction. Lastly, we observed an age-related reduction in recombination among the meiosis I cases, with older women having less recombination along 21q than younger women. Thus, reduced genetic recombination may be responsible, at least in part, for the association between advancing maternal age and trisomy 21.
对300多例21三体综合征病例进行了分析,以确定母亲减数分裂不分离的原因,并评估母亲年龄依赖性21三体综合征的基础。我们证实了在未分离的21号染色体上沿21q的重组减少这一观察结果,并进一步证明重组的改变仅限于减数分裂I起源。交叉分布分析表明,重组减少并非仅仅是由于一部分病例中配对失败和/或无重组。相反,我们观察到在产生21三体的减数分裂中零交换和单交换事件均增加,这表明重组的总体减少可能是不分离的根本原因。最后,我们观察到减数分裂I病例中重组随年龄的减少,年长女性沿21q的重组比年轻女性少。因此,遗传重组减少可能至少部分地导致了母亲年龄增长与21三体综合征之间的关联。