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体外受精产生的多核受精卵的染色体组成。

The chromosomal constitution of multipronuclear zygotes resulting from in-vitro fertilization.

作者信息

Rosenbusch B, Schneider M, Sterzik K

机构信息

Department of Gynecology and Obstetrics, University of Ulm, Ulm/Donau, Germany.

出版信息

Hum Reprod. 1997 Oct;12(10):2257-62. doi: 10.1093/humrep/12.10.2257.

Abstract

We have attempted to analyse the chromosome constitution of 77 multipronuclear uncleaved zygotes obtained from our in-vitro fertilization programme. Complete karyotypes could be established for 51 tripronuclear cells and eight zygotes with four pronuclei. When compiling the results, the varying arrangement of the chromosome sets was taken into consideration. Eighteen tripronuclear zygotes showed three separate haploid metaphases (distribution pattern n/n/n), 16 cells had one haploid and one diploid chromosome set (n/2n), and in 15 zygotes the individual sets were not distinguishable (3n). Two zygotes were in fact tetraploid, the distribution of metaphases on the slide being n/3n and n/n/2n, respectively. In tripronuclear zygotes the sex chromosome ratio XXX:XXY:XYY was 14:16:18, excluding the two tetraploid cells and one zygote with a 23,X/23,X/22,-C or -Y karyotype. Chromosome abnormalities were found in 16 zygotes (31.4%) and included numerical (six cells), structural (four cells) as well as combinations of numerical and structural alterations (six cells). Four of the zygotes with four pronuclei (50%) had numerical and/or structural chromosome aberrations. Excluding two cells with one uninterpretable metaphase and a 22,-C or -Y karyotype, respectively, the sex chromosome distribution XXXX:XXXY:XXYY:XYYY was 1:1:2:1 in zygotes with four pronuclei. Another zygote was found to be pentaploid after fixation. These results suggest that analysis of multipronuclear zygotes yields valuable information about cytogenetic abnormalities occurring at the earliest stage of conception.

摘要

我们试图分析从体外受精项目中获得的77个多核未分裂受精卵的染色体组成。可以为51个三核细胞和8个四核受精卵建立完整的核型。在汇总结果时,考虑了染色体组的不同排列方式。18个三核受精卵显示出三个独立的单倍体中期(分布模式为n/n/n),16个细胞有一个单倍体和一个二倍体染色体组(n/2n),15个受精卵中的各个染色体组无法区分(3n)。两个受精卵实际上是四倍体,玻片上中期的分布分别为n/3n和n/n/2n。在三核受精卵中,性染色体比例XXX:XXY:XYY为14:16:18,不包括两个四倍体细胞和一个核型为23,X/23,X/22,-C或-Y的受精卵。在16个受精卵(31.4%)中发现了染色体异常,包括数目异常(6个细胞)、结构异常(4个细胞)以及数目和结构改变的组合(6个细胞)。4个四核受精卵(50%)有数目和/或结构染色体畸变。分别排除两个中期无法解读且核型为22,-C或-Y的细胞后,四核受精卵中性染色体分布XXXX:XXXY:XXYY:XYYY为1:1:2:1。另一个受精卵在固定后被发现是五倍体。这些结果表明,对多核受精卵的分析能提供有关受孕最早阶段发生的细胞遗传学异常的有价值信息。

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