Development of TaqMan allelic discrimination based genotyping of large DNA deletions

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• 作者：Anastasia Fedick^a ; ^{afedick@rmanj.com} ; Jing Su^b ; Nathan R. Treff^a ; ^b
• 关键词：TaqMan allelic discrimination ; Genotyping ; Deletion mutation ; Ashkenazi
• 刊名：Genomics
• 出版年：2012
• 期刊代码：170_08887543
• 类别：bio
• 出版时间：March, 2012
• 卷：99
• 期：3
• 页码：127-131
• 文件大小：594 K

摘要

The high prevalence of genetic diseases resulting from gross deletions has highlighted a need for a quick, simple, and reliable method of genotyping these mutations. Here, we developed a novel strategy for applying TaqMan allelic discrimination to accurately genotype 3 different large deletions in a high-throughput manner. Allelic discrimination has previously been used to genotype frame shift and point mutations, and small insertions or deletions six base pairs in length, but not large deletions. The assays designed here recognize a 2502 base pair deletion in the Nebulin (NEB) gene that results in Nemaline Myopathy, a 308,769 base pair deletion in the Gap Junction Protein, beta 6 (GJB6) gene that causes Hearing Loss, and a 6433 base pair deletion in the Mucolipin 1 (MCOLN1) gene responsible for causing Mucolipidosis IV Disease. This methodology may also be successfully applied to high throughput genotyping of other large deletions.