豇豆(Vigna mungo (L.))遗传变异对比揭示及遗传多样性研究Hepper)利用SDS-PAGE分析种子贮藏蛋白

S. Tripathy, P. Mohanty, M. Jena, G. Dash, K. Pradhan, P. Nayak, S. Dash, D. Lenka, D. Mishra, P. Mohapatra, D. Swain, N. Senapati
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引用次数: 6

摘要

采用十二烷基硫酸钠聚丙烯酰胺凝胶电泳(SDS-PAGE)技术对包括流行品种T9在内的20个豇豆基因型的总种子贮藏蛋白谱进行了分析。基于基因型特异性的种子蛋白指纹图谱可明确鉴定出14个基因型,其余试验基因型可划分为3种蛋白型。基于电泳数据的树状图将基因型聚为7组,表型水平为78.5%。TU 95-1与TU 12-25-4相似指数最低(0.33),其次是TU 95-1与PU 30和KU 96-3(SI=0.35)。聚类结果显示,TPU 95-1与TPU 4形成明显的分化群。这些基因型可以作为重组育种中有价值的源基因型。关键词:种子贮藏蛋白谱,SDS-PAGE,遗传变异,豇豆
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Revealing contrasting genetic variation and study of genetic diversity in urdbean (Vigna mungo (L.) Hepper) using SDS-PAGE of seed storage proteins
Total seed storage protein profiles of 20 urdbean genotypes including the popular variety T9 were analysed by Sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE). 14 genotypes could be clearly identified based on genotype-specific seed protein fingerprints while rest of the test genotypes were categorized into three protein types. Dendrogram based on electrophoretic data clustered the genotypes into seven groups at 78.5% phenon level.  TU 95-1 with TU 12-25-4 revealed lowest similarity index value (0.33) followed by TU 95-1 with PU 30 and KU 96-3(SI=0.35). Clustering pattern revealed distinctly divergent group formed by TPU 95-1 and TPU 4. These may serve as a valuable source genotype in recombination breeding. Key words: Seed storage protein profiling, SDS-PAGE, Genetic variation, urdbean.
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