A rapid quantitative real-time PCR-based DNA quantification assay coupled with species--assignment capabilities for two hybridizing Macaca species.

A Barr, A Premasuthan, J Satkoski, D G Smith, D George, S Kanthaswamy
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引用次数: 11

Abstract

Regional populations of rhesus and long-tailed macaques exhibit fundamental differences in mitochondrial DNA, short tandem repeat and single nucleotide polymorphism variation between mainland and insular Southeast Asian populations. Some studies have revealed genetic admixture between these species due to natural hybridization and human-assisted intercrosses. A quantitative real-time PCR (qPCR) assay was developed to efficiently determine the species of origin of a macaque biological sample, and to quantify the species-specific template DNA. Prior knowledge of species identity and DNA concentrations are crucial for maintaining cost-effective methods and accurate DNA analysis. DNA from 109 regionally representative rhesus and long-tailed macaques was qPCR amplified to determine the species and template quantities. Of the 19 Vietnamese long-tailed macaques, 3 samples were discovered to be hybrids.

一个快速定量实时pcr为基础的DNA定量分析结合物种分配能力的两个杂交猕猴物种。
恒河猴和长尾猕猴的区域种群在线粒体DNA、短串联重复序列和单核苷酸多态性变异方面与东南亚大陆和岛屿种群存在根本差异。一些研究表明,这些物种之间存在遗传混合,这是由于自然杂交和人类辅助杂交。建立了一种实时荧光定量PCR (qPCR)方法,用于确定猕猴生物样本的来源物种,并定量确定物种特异性模板DNA。物种身份和DNA浓度的先验知识对于维持成本效益的方法和准确的DNA分析至关重要。采用qPCR方法扩增了109只地区代表性恒河猴和长尾猕猴的DNA,以确定其种类和模板数量。在19只越南长尾猕猴中,有3只样本为杂交。
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