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罗伯逊易位杂合女性携带者后代中的传递比率畸变。

Transmission ratio distortion in offspring of heterozygous female carriers of Robertsonian translocations.

作者信息

Pardo-Manuel de Villena F, Sapienza C

机构信息

Fels Institute for Cancer Research and Molecular Biology, Temple University School of Medicine, Philadelphia, PA 19140, USA.

出版信息

Hum Genet. 2001 Jan;108(1):31-6. doi: 10.1007/s004390000437.

Abstract

Robertsonian translocations are the most common structural rearrangements of human chromosomes. Although segregation of Robertsonian chromosomes has been examined in many families, there is little consensus on whether inheritance in the balanced progeny conforms to Mendelian ratios. To address this question, we have compiled previously reported segregation data, by sex of parent, for 677 balanced offspring of Robertsonian carriers from 82 informative families and from a prenatal diagnosis study on the risk of unbalanced offspring in carriers of chromosome rearrangements. Care was taken to avoid any source of ascertainment bias. Our analysis supports the following conclusions: (1) the transmission ratio is not independent of the sex of the carrier; (2) the transmission ratio distortion is observed consistently only among the offspring of carrier females; (3) the transmission ratio distortion does not appear to be dependent on the presence of a specific acrocentric chromosome in the rearrangement. The sex-of-parent-specific origin of the non-Mendelian inheritance, the finding that the rearranged ("mutant") chromosomes are recovered at significantly higher frequency than the acrocentric ("normal") chromosomes, and the similarities between these observations and the segregation of analogous rearrangements through female meiosis in other vertebrates strongly support the hypothesis that the transmission ratio distortion in favor of Robertsonian translocations in the human results from the preferential segregation of chromosomes during the first meiotic division. This non-Mendelian inheritance will result in increased overall risk of aneuploidies in the families of Robertsonian translocation carriers, independently of the origin of the transmission ratio distortion.

摘要

罗伯逊易位是人类染色体最常见的结构重排。尽管在许多家族中都对罗伯逊染色体的分离进行了研究,但对于平衡后代的遗传是否符合孟德尔比率,几乎没有达成共识。为了解决这个问题,我们收集了先前报道的按父母性别分类的分离数据,这些数据来自82个信息丰富的家族中的罗伯逊易位携带者的677名平衡后代,以及一项关于染色体重排携带者中不平衡后代风险的产前诊断研究。我们小心避免任何确定偏倚的来源。我们的分析支持以下结论:(1)传递比率并非独立于携带者的性别;(2)传递比率畸变仅在携带者女性的后代中持续观察到;(3)传递比率畸变似乎并不取决于重排中特定近端着丝粒染色体的存在。非孟德尔遗传的父母性别特异性起源、重排(“突变”)染色体以显著高于近端着丝粒(“正常”)染色体的频率被回收这一发现,以及这些观察结果与其他脊椎动物通过雌性减数分裂进行的类似重排分离之间的相似性,有力地支持了这样一种假说,即人类中有利于罗伯逊易位的传递比率畸变是由于第一次减数分裂期间染色体的优先分离所致。这种非孟德尔遗传将导致罗伯逊易位携带者家族中整体非整倍体风险增加,而与传递比率畸变的起源无关。

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