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首页> 外文期刊>Archives of Biological Sciences >COMPARISON OF SINGLE NUCLEOTIDE POLYMORPHISMS AND MICROSATELLITES IN NON-INVASIVE GENETIC MONITORING OF A WOLF POPULATION
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COMPARISON OF SINGLE NUCLEOTIDE POLYMORPHISMS AND MICROSATELLITES IN NON-INVASIVE GENETIC MONITORING OF A WOLF POPULATION

机译:狼群非侵入性遗传监测中单个核苷酸多态性与微卫星的比较

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Single nucleotide polymorphisms (SNPs) which represent the most widespread source of sequence variation in genomes, are becoming a routine application in several fields such as forensics, ecology and conservation genetics. Their use, requiring short amplifications, may allow a more efficient genotyping of degraded DNA. We provide the first application of SNP genotyping in an Italian non-invasive genetic monitoring project of the wolf. We compared three different techniques for genotyping SNPs: pyrosequencing, SNaPshot? and TaqMan? Probe Assay in Real-Time PCR. We successively genotyped nine SNPs using the TaqMan Probe Assay in 51 Italian wolves, 57 domestic dogs, 15 wolf x dog hybrids and 313 wolf scats collected in the northern Apennines. The obtained results were used to estimate genetic variability and PCR error rates in SNP genotyping protocols compared to standard microsatellite analysis. We evaluated the cost, laboratory effort and reliability of these different markers and discuss the possible future use of VeraCode, SNPlex and Fluidigm EP1 system in wild population monitoring.
机译:单核苷酸多态性(SNP)代表了基因组中序列变异的最广泛来源,正在成为法医,生态学和保护遗传学等多个领域的常规应用。它们的使用需要短的扩增,可以允许对降解的DNA进行更有效的基因分型。我们提供了SNP基因分型在狼的意大利无创遗传监测项目中的首次应用。我们比较了三种不同的SNP基因分型技术:焦磷酸测序,SNaPshot?和TaqMan?实时PCR中的探针测定。我们使用TaqMan探针分析法成功地对9个SNP进行了基因分型,它们来自于亚平宁山脉北部收集的51只意大利狼,57只家犬,15只狼x狗杂种和313只狼。与标准微卫星分析相比,获得的结果用于估计SNP基因分型方案中的遗传变异性和PCR错误率。我们评估了这些不同标记的成本,实验室工作量和可靠性,并讨论了VeraCode,SNPlex和Fluidigm EP1系统在野生种群监测中的未来用途。

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