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通过使用复合全染色体特异性DNA探针的三联组合进行荧光原位杂交分析辐射诱导的染色体畸变。

Radiation-induced chromosome aberrations analysed by fluorescence in situ hybridization with a triple combination of composite whole chromosome-specific DNA probes.

作者信息

Schmid E, Zitzelsberger H, Braselmann H, Gray J W, Bauchinger M

机构信息

Institut für Strahlenbiologie, GSF-Forschungszentrum für Umwelt und Gesundheit, Neuherberg, Germany.

出版信息

Int J Radiat Biol. 1992 Dec;62(6):673-8. doi: 10.1080/09553009214552621.

Abstract

Fluorescence in situ hybridization (FISH) with a combination of three composite whole chromosome-specific DNA probes for human chromosomes 1, 4 and 12 was used to analyse in vitro radiation-induced dicentrics and symmetrical translocations in peripheral lymphocytes. Translocations could be rapidly and efficiently detected by FISH. Their frequencies were 1.8-fold higher than the frequencies for dicentrics at a given dose. The dose-response curves for translocations and dicentrics were linear quadratic with a significant higher quadratic component for translocations. The application of FISH for scoring stable translocations for biological dosimetry of radiation exposures is discussed.

摘要

采用针对人类1号、4号和12号染色体的三种复合全染色体特异性DNA探针组合进行荧光原位杂交(FISH),以分析体外辐射诱导的外周血淋巴细胞中的双着丝粒和对称易位。通过FISH可以快速有效地检测到易位。在给定剂量下,易位频率比双着丝粒频率高1.8倍。易位和双着丝粒的剂量反应曲线均为线性二次曲线,易位的二次成分显著更高。讨论了FISH在辐射暴露生物剂量测定中用于稳定易位评分的应用。

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