Rapid single-tube splice variants typing of the BF gene based on dual-primer RT-PCR amplification that influence resistance/susceptibility to Mareks disease in chicken

Jin Yuan-chang, Li Yu-feng, H. Liang, Zhou Jia-jun, Zhang Xue-fang, M. Ran, Lu Meng-lin, Hao Mei-lin, Zeng Gang, Zeng Bo-ping
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引用次数: 0

Abstract

A new effective splice variants typing based on multiplex allele-specific dual-primer RT-PCR assay was developed in a single tube for the rapid detection of the exon 7 splice variant of the BF gene. With 2 pairs of primers, one pair was used for amplifying cDNA fragments containing exon 7 of the BF gene, the other does not contain exon 7 of the BF gene. The templates were amplified in one tube and the type of splice variants was determined by the length of products to be extended and by analysis of nucleotide sequences of these BFs. Results obtained for all samples showed 100% accuracy compared to those obtained with a semi-nested PCR (snPCR) assay of 100% accuracy, but which need two round PCR assay. The dual-primer RT-PCR assay was more rapid and easy to operate than the snPCR assay.
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基于双引物RT-PCR扩增的BF基因快速单管剪接变异体分型对鸡马立克氏病抗性/易感性的影响
为了快速检测BF基因外显子7剪接变异,建立了一种新的基于多重等位基因特异性双引物RT-PCR的剪接变异分型方法。用2对引物,一对用于扩增含有BF基因7外显子的cDNA片段,另一对不含BF基因7外显子。在一个试管中扩增模板,通过扩增产物的长度和分析这些BFs的核苷酸序列来确定剪接变体的类型。与半巢式PCR (snPCR)测定100%的准确性相比,所有样品的结果均显示100%的准确性,但需要两次轮PCR测定。双引物RT-PCR比snPCR快速、简便。
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来源期刊
African Journal of Biotechnology
African Journal of Biotechnology 工程技术-生物工程与应用微生物
自引率
0.00%
发文量
15
审稿时长
4.7 months
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