Hagiwara Hiroko, Sawakami-Kobayashi Kazumi, Yamamoto Midori, Iwasaki Shoji, Sugiura Mika, Abe Hatsumi, Kunihiro-Ohashi Sumiko, Takase Kumiko, Yamane Noriko, Kato Kaoru, Son Renkon, Nakamura Michihiro, Segawa Osamu, Yoshida Mamiko, Yohda Masafumi, Tajima Hideji, Kobori Masato, Takahama Yousuke, Itakura Mitsuo, Machida Masayuki
Advanced Institute of Industrial Science and Technology (AIST), Japan.
Biotechnol Bioeng. 2007 Oct 1;98(2):420-8. doi: 10.1002/bit.21380.
Biological and medical importance of the single nucleotide polymorphism (SNP) has led to development of a wide variety of methods for SNP typing. Aiming for establishing highly reliable and fully automated SNP typing, we have developed the adapter ligation method in combination with the paramagnetic beads handling technology, Magtration(R). The method utilizes sequence specific ligation between the fluorescently labeled adapter and the sample DNAs at the cohesive end produced by a type IIS restriction enzyme. Evaluation of the method using human genomic DNA showed clear discrimination of the three genotypes without ambiguity using the same reaction condition for any SNPs examined. The operations following PCR amplification were automatically performed by the Magtration(R)-based robot that we have previously developed. Multiplex typing of two SNPs in a single reaction by using four fluorescent dyes was successfully preformed at the almost same sensitivity and reliability as the single typing. These results demonstrate that the automated paramagnetic beads handling technology, Magtration(R), is highly adaptable to the automated SNP analysis and that our method best fits to an automated in-house SNP typing for laboratory and medical uses.
单核苷酸多态性(SNP)在生物学和医学上的重要性促使人们开发了各种各样的SNP分型方法。为了建立高度可靠且完全自动化的SNP分型方法,我们结合顺磁珠处理技术Magtration®开发了衔接子连接法。该方法利用荧光标记的衔接子与由IIS型限制酶产生的粘性末端处的样品DNA之间的序列特异性连接。使用人类基因组DNA对该方法进行评估表明,对于所检测的任何SNP,在相同反应条件下都能清晰区分三种基因型,不存在模糊性。PCR扩增后的操作由我们之前开发的基于Magtration®的机器人自动执行。使用四种荧光染料在单个反应中对两个SNP进行多重分型,其灵敏度和可靠性与单分型几乎相同。这些结果表明,自动化顺磁珠处理技术Magtration®非常适合自动化SNP分析,并且我们的方法最适合用于实验室和医学用途的自动化内部SNP分型。