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首页> 外文期刊>The Veterinary Journal >Detection of the nt230[del4] MDR1 mutation in dogs by a fluorogenic 5' Nuclease TaqMan allelic discrimination method.
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Detection of the nt230[del4] MDR1 mutation in dogs by a fluorogenic 5' Nuclease TaqMan allelic discrimination method.

机译:用荧光5'核酸酶TaqMan等位基因鉴别方法检测狗中nt230 [del4] MDR1 突变。

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摘要

For detection of the nt230[del4] MDR1 mutation, a 4-bp deletion in the canine MDR1 (ABCB1) gene, a TaqMan allelic discrimination assay was designed that allows for MDR1 genotyping without post-PCR processing. Directly after completion of the PCR amplification, the MDR1 genotype can be assigned based on selective fluorescence measurement. For primer selection the locus of a potential 265A > G single nucleotide polymorphism was omitted; this locus is covered by the oligonucleotide PCR primers from most of the hitherto established MDR1 genotyping methods. Dogs homozygous for the nt230[del4] MDR1 mutation show highly increased susceptibility to many drugs commonly used in veterinary medicine including ivermectin. As more than 10 dog breeds are predisposed to this mutation, reliable genotyping methods are necessary to identify affected dogs before drug treatment. This study provides a new allelic discrimination method that detects the MDR1 mutation with high specificity and reliability and is useful for routine diagnostics.
机译:为了检测nt230 [del4] MDR1 突变,即犬 MDR1(ABCB1)基因中的4 bp缺失,设计了TaqMan等位基因判别分析,该分析可实现< i> MDR1 基因分型,无需进行PCR后处理。 PCR扩增完成后,可以直接基于选择性荧光测量来分配 MDR1 基因型。对于引物选择,省略了潜在的265A> G单核苷酸多态性的基因座。该基因座被迄今为止大多数已建立的 MDR1 基因分型方法的寡核苷酸PCR引物所覆盖。纯合nt230 [del4] MDR1 突变的狗对包括伊维菌素在内的许多兽医学常用药物的敏感性大大提高。由于超过10种犬种容易发生这种突变,因此在药物治疗之前必须有可靠的基因分型方法来鉴定出患病的狗。这项研究提供了一种新的等位基因鉴别方法,该方法可高度特异性和可靠性地检测 MDR1 突变,可用于常规诊断。

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