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通过引物原位标记串联标记法检测胞质分裂阻滞小鼠脾细胞中的小卫星和主要卫星DNA。

Detection of minor and major satellite DNA in cytokinesis-blocked mouse splenocytes by a PRINS tandem labelling approach.

作者信息

Russo A, Tommasi A M, Renzi L

机构信息

Department of Biology, University of Padova, Italy.

出版信息

Mutagenesis. 1996 Nov;11(6):547-52. doi: 10.1093/mutage/11.6.547.

Abstract

A protocol for the simultaneous visualization of minor and major satellite DNA by primed in situ DNA synthesis (PRINS) was developed in cytokinesis-blocked murine splenocytes. After individuation of optimal experimental conditions, a micronucleus (MN) test was carried out by treating splenocytes in vitro with the clastogenic agent mitomycin C and the aneugenic compound Colcemid. It was found that PRINS gives highly reproducible results, also comparable with the literature on MN results obtained by fluorescent in situ hybridization (FISH). Therefore the PRINS methodology may be proposed as a fast alternative to FISH for the characterization of induced MN.

摘要

在胞质分裂阻滞的小鼠脾细胞中开发了一种通过引物原位DNA合成(PRINS)同时可视化小卫星和主要卫星DNA的方案。在确定最佳实验条件后,通过用致断裂剂丝裂霉素C和非整倍体化合物秋水仙酰胺体外处理脾细胞进行微核(MN)试验。结果发现,PRINS能给出高度可重复的结果,也与荧光原位杂交(FISH)获得的MN结果的文献相当。因此,PRINS方法可作为FISH的一种快速替代方法,用于鉴定诱导产生的微核。

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