Electrophoretic Mobility of Amplified Products at MCT118 Locus.

G. Watanabe
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Abstract

DNA typing of MCT118 (D1S80) locus has been performed with polyacrylamide gel electrophoresis using D1S80 allelic ladder. However, some oŠ-ladder variants, which showed diŠerent electrophoretic mobility compared with the allelic ladder, were observed frequently in MCT118 typing. Five variants from ˆve previously typed individuals were selected for sequence analysis. The sequence of the variants were determined to ascertain whether sequence variation or size variation is the cause of altered migration of the oŠ-ladder variants. All of the variants have nucleotide substitutions resulting in diŠerent sequences of some repeat units and do not have insertions or deletions. Consequently, the MCT118 allelic polymorphism is due to variation in the number of repeat units and to sequence variation among repeats. Furthermore, we examined electrophoresis conditions in order to accurately determine the type of MCT118. Under suitable electrophoresis conditions, all of the variants were typed as corresponding alleles within ±0.15 repeats.
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MCT118位点扩增产物的电泳迁移率。
采用D1S80等位基因阶梯对MCT118 (D1S80)基因座进行聚丙烯酰胺凝胶电泳分型。然而,在MCT118分型中经常观察到一些oŠ-ladder变异,与等位基因阶梯相比,它们表现出diŠerent的电泳迁移率。从5个先前分型的个体中选择5个变体进行序列分析。确定变异的序列以确定是序列变异还是大小变异是导致oŠ-ladder变异迁移改变的原因。所有的变异都有核苷酸替换,导致一些重复单元的diŠerent序列,并且没有插入或删除。因此,MCT118等位基因多态性是由于重复单位数量的变化和重复之间的序列变化。此外,我们检查了电泳条件,以准确地确定MCT118的类型。在合适的电泳条件下,所有变异在±0.15个重复内被分型为对应的等位基因。
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