Suppr超能文献

罗伯逊易位携带者精子中,分离模式改变与染色体数目异常相互关联。

Altered segregation pattern and numerical chromosome abnormalities interrelate in spermatozoa from Robertsonian translocation carriers.

作者信息

Godo Anna, Blanco Joan, Vidal Francesca, Sandalinas Mireia, Garcia-Guixé Elena, Anton Ester

机构信息

Genetics of Male Fertility Group, Unitat de Biologia Cel⋅lular (Facultat de Biociències), Universitat Autònoma de Barcelona, 08193 Bellaterra, Cerdanyola del Vallès, Spain.

Reprogenetics Spain, Carrer Tuset, 23, 08006 Barcelona, Spain.

出版信息

Reprod Biomed Online. 2015 Jul;31(1):79-88. doi: 10.1016/j.rbmo.2015.04.003. Epub 2015 Apr 16.

Abstract

The aim of this study was to assess whether there is a relationship between numerical chromosome abnormalities and certain segregation modes in spermatozoa from Robertsonian translocation carriers. A sequential fluorescence in-situ hybridization protocol based on two successive hybridization rounds was performed on sperm samples from one t(13;22) and ten t(13;14) carriers. Patient inclusion criteria included the presence of a positive interchromosomal effect (ICE). In the first round, numerical abnormalities for chromosomes 15/22, 18, 21, X and Y were analysed. In the second round, the segregation outcome of the rearranged chromosomes was evaluated in the numerically abnormal spermatozoa detected in the first round, as well as in randomly assessed spermatozoa. Aneuploid spermatozoa showed statistical differences in all segregation modes when compared with randomly assessed spermatozoa: alternate (50.7% versus 84.3%), adjacent (36.6% versus 14.6%) and 3:0 (10.2% versus 1%). Diploid/multiple disomic spermatozoa showed differences in alternate (3.7% versus 84.3%) and 3:0 (67.6% versus 1%). We concluded that in Robertsonian translocation carriers that exhibit ICE, numerically abnormal spermatozoa preferentially contain unbalanced segregation products. This might be explained by heterosynapsis acting as a rescue mechanism that would lead to aberrant recombination, which is a predisposing factor for non-disjunction events.

摘要

本研究的目的是评估罗伯逊易位携带者精子中的染色体数目异常与某些分离模式之间是否存在关联。对一名t(13;22)携带者和十名t(13;14)携带者的精子样本进行了基于两轮连续杂交的序贯荧光原位杂交实验。患者纳入标准包括存在阳性染色体间效应(ICE)。在第一轮中,分析了15/22、18、21、X和Y染色体的数目异常情况。在第二轮中,对第一轮检测到的染色体数目异常精子以及随机评估的精子中重排染色体的分离结果进行了评估。与随机评估的精子相比,非整倍体精子在所有分离模式下均表现出统计学差异:交替分离(50.7%对84.3%)、相邻分离(36.6%对14.6%)和3:0分离(10.2%对1%)。二倍体/多重双体精子在交替分离(3.7%对84.3%)和3:0分离(67.6%对1%)方面存在差异。我们得出结论,在表现出ICE的罗伯逊易位携带者中,染色体数目异常的精子优先包含不平衡的分离产物。这可能是由于异源联会作为一种挽救机制,导致异常重组,而异常重组是非分离事件的一个诱发因素。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验