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在人类卵子发生过程中探寻14号和21号染色体之间的近端着丝粒关联

FISHing for acrocentric associations between chromosomes 14 and 21 in human oogenesis.

作者信息

Cheng Edith Y, Naluai-Cecchini Theresa

机构信息

Departments of Obstetrics and Gynecology and Medicine, University of Washington, Seattle, 98195-6460, USA.

出版信息

Am J Obstet Gynecol. 2004 Jun;190(6):1781-5; discussion 1785-7. doi: 10.1016/j.ajog.2004.02.062.

Abstract

OBJECTIVE

The purpose of this study was to search for cytologic evidence of robertsonian translocation formation that involves chromosomes 14q and 21q in human oogenesis with the use of dual color fluorescent in situ hybridization with whole chromosome paints.

STUDY DESIGN

The oocytes from a chromosomally normal fetus at 23.5 weeks of gestation underwent cohybridization with chromosome specific DNA libraries from chromosomes 14 and 21. The nuclei were scored for the proportion of meiosis I prophase substages and for hybridization efficiency and were evaluated for the presence of hybridization signals that were suggestive of heterologous associations between chromosomes 14q and 21q in zygotene, pachytene, and diplotene.

RESULTS

A total of 1769 meiotic nuclei were analyzed. Of 272 informative nuclei at zygotene, pachytene, and diplotene, 1 nucleus at pachytene demonstrated hybridization signals for chromosomes 14 and 21 that could be consistent with a robertsonian translocation.

CONCLUSION

A heterologous association between chromosomes 14q and 21q that possibly represent robertsonian translocation formation was observed cytologically with the use of fluorescent in situ hybridization.

摘要

目的

本研究的目的是通过使用全染色体涂染双色荧光原位杂交技术,寻找在人类卵子发生过程中涉及14号染色体长臂(14q)和21号染色体长臂(21q)的罗伯逊易位形成的细胞学证据。

研究设计

对一名妊娠23.5周的染色体正常胎儿的卵母细胞,进行与14号和21号染色体特异性DNA文库的共杂交。对细胞核进行减数分裂I前期亚阶段比例和杂交效率评分,并评估在偶线期、粗线期和双线期是否存在提示14q和21q染色体之间异源关联的杂交信号。

结果

共分析了1769个减数分裂细胞核。在272个处于偶线期、粗线期和双线期的可提供信息的细胞核中,有1个处于粗线期的细胞核显示出与罗伯逊易位相符的14号和21号染色体杂交信号。

结论

使用荧光原位杂交技术在细胞学上观察到了14q和21q染色体之间可能代表罗伯逊易位形成的异源关联。

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