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使用生物素化探针原位杂交检测正常和变异人类染色体中的Y特异性重复序列。

Detection of Y-specific repeat sequences in normal and variant human chromosomes using in situ hybridization with biotinylated probes.

作者信息

Lau Y F

出版信息

Cytogenet Cell Genet. 1985;39(3):184-7. doi: 10.1159/000132132.

Abstract

In situ hybridization with a cloned human Y-specific repeat, pY3.4, derived from the 3.4-kb HaeIII repetitive sequences, is useful in identifying Yq-autosome translocations. In this study nonradioactive procedures were also employed to detect the sites of hybridization. Using a biotinylated probe and either immunofluorescence or horseradish peroxidase reaction, the chromosomes of three probands and members of their families with probable Y-autosome translocations were examined. It was found that not all such translocations can be correctly diagnosed based on conventional banding analysis. The present data indicate the importance of chromosome-specific probes in studying chromosome rearrangements in man.

摘要

用从3.4kb HaeIII重复序列衍生而来的克隆化人Y特异性重复序列pY3.4进行原位杂交,有助于识别Yq-常染色体易位。在本研究中,还采用了非放射性方法来检测杂交位点。使用生物素化探针以及免疫荧光或辣根过氧化物酶反应,对三个先证者及其可能存在Y-常染色体易位的家庭成员的染色体进行了检查。结果发现,并非所有此类易位都能基于传统的显带分析得到正确诊断。目前的数据表明了染色体特异性探针在研究人类染色体重排中的重要性。

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