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Efficiency and accuracy of PCR-based sex determination methods in the european phalacrocoracidae

机译:基于效率的PCR性别测定方法在欧洲的phalacrocoracidae中

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The applicability of simple PCR-based approaches for sex discrimination in the three European Phalacrocoracidae species was tested, using 93 individuals of known sex and two sets of primers (1237L/1272R and 2550F/2718R) for the amplification of the avian sex-specific chromo-helicase-DNA-binding protein gene. We evaluated the accuracy of each set of primers in providing the correct sex for each individual. The first primer set did not produce reliable results. The second provided a band pattern for each sex, easily distinguishable with agarose gel electrophoresis, which correctly identified all the individuals, even in samples of low DNA yield. The amplification products were sequenced and aligned revealing important nucleotide diversity among Phalacrocoracidae species. Compared with morphometric discriminant analysis and DNA-fingerprinting techniques previously applied, the PCR-based sexing with the 2550F/2718R primers is more accurate, less invasive and widely applicable to both adults and chicks, using a variety of DNA sources such as blood, tissue, feathers, egg shells and others.
机译:测试了简单的基于PCR的方法在三种欧洲European草科物种中的性别歧视的适用性,使用了93名已知性别的个体和两组引物(1237L / 1272R和2550F / 2718R)来扩增禽类特定的染色体-解旋酶-DNA结合蛋白基因。我们评估了每组引物在为每个个体提供正确性别方面的准确性。第一组引物未产生可靠的结果。第二种为每种性别提供了条带模式,可通过琼脂糖凝胶电泳轻松区分,即使在DNA产量低的样品中,琼脂糖凝胶电泳也能正确识别所有个体。对扩增产物进行测序和比对,揭示了ala草科物种之间重要的核苷酸多样性。与先前应用的形态计量判别分析和DNA指纹技术相比,使用2550F / 2718R引物进行的基于PCR的性别鉴定更准确,更具侵入性,并且可以使用多种DNA来源(例如血液,组织)广泛应用于成年和雏鸡,羽毛,蛋壳等。

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