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High-resolution melting analysis for bird sexing: A successful approach to molecular sex identification using different biological samples

机译:鸟类性别的高分辨率融解分析:使用不同生物样品鉴定分子性别的成功方法

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High-resolution melting (HRM) analysis is a very attractive and flexible advanced post-PCR method with high sensitivity/specificity for simple, fast and cost-effective genotyping based on the detection of specific melting profiles of PCR products. Next generation real-time PCR systems, along with improved saturating DNA-binding dyes, enable the direct acquisition of HRM data after quantitative PCR. Melting behaviour is particularly influenced by the length, nucleotide sequence and GC content of the amplicons. This method is expanding rapidly in several research areas such as human genetics, reproductive biology, microbiology and ecology/conservation of wild populations. Here we have developed a successful HRM protocol for avian sex identification based on the amplification of sex-specific CHD1 fragments. The melting curve patterns allowed efficient sexual differentiation of 111 samples analysed (plucked feathers, muscle tissues, blood and oral cavity epithelial cells) of 14 bird species. In addition, we sequenced the amplified regions of the CHD1 gene and demonstrated the usefulness of this strategy for the genotype discrimination of various amplicons (CHD1Z and CHD1W), which have small size differences, ranging from 2 bp to 44 bp. The established methodology clearly revealed the advantages (e.g. closed-tube system, high sensitivity and rapidity) of a simple HRM assay for accurate sex differentiation of the species under study. The requirements, strengths and limitations of the method are addressed to provide a simple guide for its application in the field of molecular sexing of birds. The high sensitivity and resolution relative to previous real-time PCR methods makes HRM analysis an excellent approach for improving advanced molecular methods for bird sexing.
机译:高分辨率熔解(HRM)分析是一种非常诱人且灵活的高级后PCR方法,具有高灵敏度/特异性,可基于检测PCR产物的特定熔解曲线进行简单,快速且经济高效的基因分型。下一代实时PCR系统以及改进的饱和DNA结合染料可以在定量PCR之后直接获取HRM数据。熔解行为特别受扩增子的长度,核苷酸序列和GC含量影响。这种方法正在人类遗传学,生殖生物学,微生物学和野生种群生态/保护等几个研究领域中迅速发展。在这里,我们已基于性别特异性CHD1片段的扩增,开发了一种成功的HRM协议,可用于禽类性别鉴定。融解曲线模式可对14种鸟类的111种样品(拔出的羽毛,肌肉组织,血液和口腔上皮细胞)进行有效的性别区分。此外,我们对CHD1基因的扩增区域进行了测序,并证明了该策略对各种扩增子(CHD1Z和CHD1W)的基因型判别的有用性,这些扩增子的大小差异在2 bp至44 bp之间。既定的方法学清楚地揭示了简单的HRM测定法对所研究物种的准确性别区分的优势(例如,封闭管系统,高灵敏度和快速性)。提出了该方法的要求,优势和局限性,为在鸟类分子性别鉴定领域中的应用提供了简单的指南。相对于以前的实时PCR方法,高灵敏度和高分辨率使HRM分析成为改善鸟类性别鉴定的先进分子方法的绝佳方法。

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