Yang Bing, Damaschke Nathan, Yao Tianyu, McCormick Johnathon, Wagner Jennifer, Jarrard David
Department of Urology, University of Wisconsin School of Medicine and Public Health, Madison, Wisconsin.
University of Wisconsin Carbone Comprehensive Cancer Center, Madison, Wisconsin.
J Cell Biochem. 2015 Jul;116(7):1165-70. doi: 10.1002/jcb.25081.
Genomic imprinting is an epigenetic mechanism that restricts gene expression to one inherited allele. Improper maintenance of imprinting has been implicated in a number of human diseases and developmental syndromes. Assays are needed that can quantify the contribution of each paternal allele to a gene expression profile. We have developed a rapid, sensitive quantitative assay for the measurement of individual allelic ratios termed Pyrosequencing for Imprinted Expression (PIE). Advantages of PIE over other approaches include shorter experimental time, decreased labor, avoiding the need for restriction endonuclease enzymes at polymorphic sites, and prevent heteroduplex formation which is problematic in quantitative PCR-based methods. We demonstrate the improved sensitivity of PIE including the ability to detect differences in allelic expression down to 1%. The assay is capable of measuring genomic heterozygosity as well as imprinting in a single run. PIE is applied to determine the status of Insulin-like Growth Factor-2 (IGF2) imprinting in human and mouse tissues.
基因组印记是一种表观遗传机制,它将基因表达限制在一个遗传等位基因上。印记的不当维持与多种人类疾病和发育综合征有关。需要能够量化每个父本等位基因对基因表达谱贡献的检测方法。我们开发了一种快速、灵敏的定量检测方法,用于测量个体等位基因比例,称为印记表达焦磷酸测序(PIE)。PIE相对于其他方法的优点包括实验时间更短、劳动强度降低、无需在多态性位点使用限制性内切酶,以及防止异源双链体形成,而异源双链体形成在基于定量PCR的方法中是个问题。我们证明了PIE的灵敏度有所提高,包括能够检测低至1%的等位基因表达差异。该检测方法能够在一次运行中测量基因组杂合性以及印记情况。PIE被应用于确定人类和小鼠组织中胰岛素样生长因子2(IGF2)的印记状态。