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通过激光显微切割和接头-衔接子PCR从单条染色体生成染色体涂染探针。

Generation of chromosome painting probes from single chromosomes by laser microdissection and linker-adaptor PCR.

作者信息

Thalhammer Stefan, Langer Sabine, Speicher Michael R, Heckl Wolfgang M, Geigl Jochen B

机构信息

Department für Geowissenschaften, University of Munich, Theresienstr. 41, D-80333 Munich, Germany.

出版信息

Chromosome Res. 2004;12(4):337-43. doi: 10.1023/B:CHRO.0000034132.77192.5f.

Abstract

Fluorescence in situ hybridization (FISH) plays an essential role in research and clinical diagnostics. The versatility and resolution of FISH depends critically on the probe set used. Here, we describe an improved approach for the generation of specific DNA probes from single copies of chromosomes. Single chromosomes or single chromosomal regions were microdissected by laser pressure catapulting and amplified using linker-adaptor PCR. The probes were labeled and tested in various scenarios including multicolor-FISH experiments employing up to seven different fluorochromes. FISH confirmed the specific and even staining of the respective chromosomal regions. Furthermore, the capability of these probes to detect even small translocations (<3 Mb) suggests that the dissected regions are completely represented in the generated painting probes.

摘要

荧光原位杂交(FISH)在研究和临床诊断中起着至关重要的作用。FISH的多功能性和分辨率关键取决于所使用的探针组。在此,我们描述了一种从单条染色体生成特异性DNA探针的改进方法。通过激光压力弹射对单条染色体或单个染色体区域进行显微切割,并使用接头连接PCR进行扩增。这些探针经过标记并在各种情况下进行测试,包括使用多达七种不同荧光染料的多色FISH实验。FISH证实了各个染色体区域的特异性和均匀染色。此外,这些探针检测甚至小至<3 Mb的易位的能力表明,在生成的涂染探针中完全代表了解剖区域。

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