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首页> 外文期刊>Breeding science >Structure and diversity of 13S globulin zero-repeat subunit, the trypsin-resistant storage protein of common buckwheat (Fagopyrum esculentum M.) seeds
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Structure and diversity of 13S globulin zero-repeat subunit, the trypsin-resistant storage protein of common buckwheat (Fagopyrum esculentum M.) seeds

机译:13s球蛋白零重复亚基的结构和多样性,普通荞麦胰蛋白酶抗性储存蛋白(Fagopyrum Esculentum M.)种子

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摘要

The zero-repeat subunit of 13S globulin, which lacks tandem repeat inserts, is trypsin-resistant and suggested to show higher allergenicity than the other subunits in common buckwheat (Fagopyrum esculentum Moench). To evaluate allelic variations and find novel alleles, the diversity of the zero-repeat genes was examined for two Japanese elite cultivars and 15 Pakistani landraces. The results demonstrated that two new alleles GIbNAI and GIbNCI, plus three additional new alleles GIbNA2, GIbNA3, and GIbND, were identified besides the already-known GIbNA, GIbNB, and GIbNC alleles. In the Pakistani landraces, Glb:VA was the most dominant allele (0.60-0.88 of allele frequency) in all except one landrace, where GIbNB was the most dominant allele (0.50 of allele frequency). Similar to GIbNC, the alleles GIbNA2 and GIbNA3 had extra similar to 200 bp MITE-like sequences around the stop codon. Secondary structure predictions of a sense strand demonstrated that the extra similar to 200 bp sequences of GIbNC, GIbNA2, and GIbNA3 can form rigid hairpin structures with free energies of -78.95, -67.06, and -29.90 kcal/mol, respectively. These structures may affect proper transcription and/or translation. In the GIbNV homozygous line, no transcript of a zero-repeat gene was detected, suggesting the material would be useful for developing hypoallergenic buckwheat.
机译:缺乏串联重复插入物的13s球蛋白的零重复亚基是胰蛋白酶抗性,并且表明含有普通荞麦(Fagopyrum Escululum Moench)中的其他亚基的过敏性。为了评估等位基因变异并找到新的等位基因,检查了两种日本精英品种和15个巴基斯坦地铁的零重复基因的多样性。结果表明,除了已知的Gibna,Gibnb和Gibnc等位基因之外,鉴定了两种新的等位基因Gibnai和Gibnci,加上三种额外的新等位基因Gibna2,Gibna3和Gibnd。在巴基斯坦地铁中,GLB:VA是除了一个Landrace之外的最主领域最多的等位基因(等位基因频率为0.60-0.88),其中Gibnb是最主载的等位基因(等位基因频率为0.50)。类似于Gibnc,等位基因Gibna2和Gibna3周围的终止密码子周围的序列与200bp螨样序列相似。感测链的二次结构预测表明,额外类似于200bp,GibnC,Gibna3的额外序列,可分别形成具有-78.95,67.06和-29.90kcal / mol的自由能量的刚性发夹结构。这些结构可能会影响正确的转录和/或翻译。在GibnV纯合线中,未检测到零重复基因的转录物,表明材料可用于开发过氧化钠荞麦。

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