White H W, Kusukawa N
FMC BioProducts, Rockland, ME, USA.
Biotechniques. 1997 May;22(5):976-80. doi: 10.2144/97225pf01.
Short tandem repeats (STRs) are traditionally analyzed on large polyacrylamide electrophoresis gels. We demonstrate in this study that a small (10-cm-long, 1-mm-thick) agarose gel is sufficient for analysis of multiplexed samples for several commonly used STR loci. A system was developed using a high-resolution agarose, MetaPhor. Within an hour of electrophoresis, sufficient resolution was obtained to allow discrimination of triple-multiplexed STR loci. We show that this agarose is capable of resolving di- as well as tetranucleotide ladders. Using PCR conditions similar to those routinely used with sensitive detection systems, we found that direct staining of gels with SYBR Green I stain was comparable with silver staining, autoradiography or fluorescently tagged primers for sample detection and was considerably easier. This procedure significantly simplifies STR analysis and is much faster than many standard protocols.
传统上,短串联重复序列(STRs)是在大型聚丙烯酰胺电泳凝胶上进行分析的。我们在本研究中证明,一块小的(10厘米长、1毫米厚)琼脂糖凝胶足以分析多个常用STR位点的多重样本。使用高分辨率琼脂糖MetaPhor开发了一个系统。在电泳一小时内,获得了足够的分辨率,能够区分三重多重STR位点。我们表明,这种琼脂糖能够分辨二核苷酸和四核苷酸阶梯。使用与灵敏检测系统常规使用的条件相似的PCR条件,我们发现用SYBR Green I染料直接对凝胶染色与银染、放射自显影或荧光标记引物用于样本检测相当,并且操作要容易得多。该方法显著简化了STR分析,并且比许多标准方案快得多。