Millis Meredith P
Diabetes, Cardiovascular, and Metabolic Diseases Division, Translational Genomics Research Institute, Phoenix, AZ, USA.
Methods Mol Biol. 2011;700:61-76. doi: 10.1007/978-1-61737-954-3_5.
Depending on the scope of the research project, categories of single-nucleotide polymorphism (SNP) genotyping experiments range from low to medium to high throughput, with each approach differing widely in cost, platform, and efficiency. Medium-throughput genotyping is generally appropriate for assaying up to 36 markers in 384 individuals and is commonly used for fine-mapping chromosomal regions identified in genome scans. Multiplexing, which allows for simultaneous assessment of multiple SNPs, is an efficient, rapid, and economic way to augment medium-throughput genotyping output and is readily performed using matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS). In this chapter, we describe a technique for medium-throughput genotyping using the iPLEX® Gold assay available from Sequenom, Inc. (San Diego, CA). This multiplex SNP genotyping platform incorporates locus-specific PCR amplification of genomic DNA, followed by shrimp alkaline phosphatase treatment to inactivate unincorporated nucleotides, single-base primer extension using mass-modified terminators, and MALDI-TOF MS for allele-specific detection. This protocol utilizes proprietary enzymes, software and SpectroCHIP® Arrays that are pre-spotted with a MALDI matrix.
根据研究项目的范围,单核苷酸多态性(SNP)基因分型实验的类别从低通量到中通量再到高通量不等,每种方法在成本、平台和效率方面差异很大。中通量基因分型通常适用于对384个个体中的多达36个标记进行检测,常用于对基因组扫描中确定的染色体区域进行精细定位。多重分析允许同时评估多个SNP,是增加中通量基因分型产量的一种高效、快速且经济的方法,并且使用基质辅助激光解吸电离飞行时间质谱(MALDI-TOF MS)很容易实现。在本章中,我们描述了一种使用Sequenom公司(加利福尼亚州圣地亚哥)提供的iPLEX® Gold分析方法进行中通量基因分型的技术。这个多重SNP基因分型平台包括对基因组DNA进行位点特异性PCR扩增,随后用虾碱性磷酸酶处理以灭活未掺入的核苷酸,使用质量修饰的终止子进行单碱基引物延伸,以及使用MALDI-TOF MS进行等位基因特异性检测。本方案使用了专有的酶、软件和预先点有MALDI基质的SpectroCHIP®阵列。