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Cloning and Sequence Analysis of Gene Fragment of Major Allergenic Protein in Tartary Buckwheat

机译:Tartary荞麦主要过敏蛋白基因片段的克隆与序列分析

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The partial gene of major allergenic protein in tartary buckwheat was amplified from the total RNA of tartary buckwheat using RT-PCR and 5'-rapid amplication of cDNA ends (5'-RACE) methods. The gene sequence consisted of 1005 nucleotides and a 960 bpopen reading frame (ORF) which encoded a protein of 320 amino acids residues. Results of homology analysis revealed that the cDNA sequence shared 90% homology with the major allergenic storage protein and legumin-like protein of common buckwheat. The deduced ammo acid sequence shared 84% and 76% homology with the legumin-like 13S storage protein and the major allergenic storage protein of common buckwheat respectively. The obtainment of gene fragment of major allergenic protein in tartary buckwheat should lay an important foundation for further study of the tartary buckwheat allergen.
机译:使用RT-PCR和5'-快速扩增cDNA末端(5'-播种)方法,从季后血荞麦酸碎片中的主要过敏蛋白的部分基因从季后荞麦酸盐的总RNA扩增。基因序列由1005个核苷酸和960bpopen读数框架(ORF)组成,其编码了320个氨基酸残基的蛋白质。同源性分析结果表明,CDNA序列与普通荞麦的主要过敏储存蛋白和豆类样蛋白共享90%同源性。推导的AMMO酸序列分别与豆类般的13S储存蛋白和分别的常见荞麦的主要过敏素储存蛋白共享84%和76%的同源性。在Tar​​tary Buckwheeat中获得主要过敏蛋白的基因片段应该为进一步研究Tartary荞麦过敏原进行重要的基础。

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