Shimizu Masashi, Kosaka Natsuki, Shimada Takashi, Nagahata Takemitsu, Iwasaki Hironori, Nagai Hisaki, Shiba Tadayoshi, Emi Mitsuru
Department of Molecular Biology, Institute of Gerontology, Nippon Medical School, 1-396 Kosugi-cho, Nakahara-ku, Kawasaki 211-8533, Japan.
DNA Res. 2002 Oct 31;9(5):173-8. doi: 10.1093/dnares/9.5.173.
We have devised a novel method for automated microsatellite analysis using "universal" fluorescent labeling. This system is based on polymerase chain reactions driven by sequence-specific primers and a reporter primer labeled with a fluorescent dye at its 5' end. The forward sequence-specific primer is designed with a tag region bearing no homology to any human genomic sequence. Complementary tag sequences act as templates for the 6-carboxyfluorescein-labeled reporter primer, and those products can be analyzed with an autosequencer. The results we achieved with this assay system were consistent with the results of conventional assays using radioisotope-labeled primers, and diagnosis required less time. Furthermore, the fluorescent-labeled reporter primer is "universal" in that it can be used with different sequence-specific primers designed to carry the appropriate tag sequence at their 5'-ends. Our observations suggest that the "universal" fluorescent labeling method is an efficient tool for analyzing sequence variations in human DNA.
我们设计了一种使用“通用”荧光标记进行自动化微卫星分析的新方法。该系统基于由序列特异性引物和在其5'端用荧光染料标记的报告引物驱动的聚合酶链反应。正向序列特异性引物设计有一个与任何人类基因组序列无同源性的标签区域。互补标签序列充当6-羧基荧光素标记的报告引物的模板,这些产物可以用自动测序仪进行分析。我们用该检测系统获得的结果与使用放射性同位素标记引物的传统检测结果一致,并且诊断所需时间更短。此外,荧光标记的报告引物是“通用的”,因为它可以与设计为在其5'端携带适当标签序列的不同序列特异性引物一起使用。我们的观察结果表明,“通用”荧光标记方法是分析人类DNA序列变异的有效工具。