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Molecular Marker-Assisted Genotyping of Mungbean Yellow Mosaic India Virus Resistant Germplasms of Mungbean and Urdbean

机译:绿豆印度花叶病抗绿豆和绿豆的分子标记辅助基因分型

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摘要

Mungbean Yellow Mosaic India Virus (MYMIV) belonging to the genus begomovirus causes the yellow mosaic disease in a number of economically important edible grain legumes including mungbean (Vigna radiata), urdbean (Vigna mungo) and soybean (Glycine max). The disease is severe, critical, open spread and inflicts heavy yield losses annually. The objective of this study is to develop molecular markers linked to MYMIV-resistance to facilitate genotyping of urdbean and mungbean germplasms for MYMIV-reaction. Resistance-linked molecular markers were successfully developed from consensus motifs of other resistance (R) gene or R gene homologue sequences. Applying linked marker-assisted genotyping, plant breeders can carry out repeated genotyping throughout the growing season in absence of any disease incidence. Two MYMIV-resistance marker loci, YR4 and CYR1, were identified and of these two CYR1 is completely linked with MYMIV-resistant germplasms and co-segregating with MYMIV-resistant F2, F3 progenies of urdbean. The present study demonstrated that these two markers could be efficiently employed together in a multiplex-PCR-reaction for genotyping both V. mungo and V. radiata germplasms from field grown plants and also directly from the seed stock. This method of genotyping would save time and labour during the introgression of MYMIV-resistance through molecular breeding, as methods of phenotyping against begomoviruses are tedious, labour and time intensive.
机译:属于begomovirus属的绿豆黄花叶印度病毒(MYMIV)在许多经济上重要的食用谷物豆类中引起黄花叶病,包括豆类(Vigna radiata),乌豆(Vigna mungo)和大豆(Glycine max)。该病是严重的,严重的,开放传播的,每年造成严重的产量损失。这项研究的目的是开发与抗MYMIV相关的分子标记,以促进针对MYMIV反应的乌豆和绿豆种质的基因分型。从其他抗性(R)基因或R基因同源序列的共有基序成功开发了抗性连锁的分子标记。应用链接的标记辅助基因分型,植物育种者可以在整个生长期进行重复的基因分型,而不会发生任何疾病。确定了两个抗MYMIV的标记基因座YR4和CYR1,这两个CYR1与抗MYMIV的种质完全连锁,并与抗MYMIV的F2 ,F3 后代共分离。本研究表明,这两种标记可以有效地一起用于多重PCR反应中,对田间生长植物以及直接从种子库中的芒(V. mungo)和辐射(V. radiata)种质进行基因分型。这种基因分型方法将通过分子育种在抗MYMIV基因渗入过程中节省时间和劳力,因为针对begomoviruss的表型分型方法既繁琐,费力又费时。

著录项

  • 来源
    《Molecular Biotechnology》 |2011年第2期|p.95-104|共10页
  • 作者单位

    Division of Plant Biology, Bose Institute, P 1/12 CIT Scheme VIIM, Kolkata, 700054, India;

    Division of Plant Biology, Bose Institute, P 1/12 CIT Scheme VIIM, Kolkata, 700054, India;

    Division of Plant Biology, Bose Institute, P 1/12 CIT Scheme VIIM, Kolkata, 700054, India;

    Division of Plant Biology, Bose Institute, P 1/12 CIT Scheme VIIM, Kolkata, 700054, India;

    Division of Plant Biology, Bose Institute, P 1/12 CIT Scheme VIIM, Kolkata, 700054, India;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    Genotyping; Molecular marker; Vignas; MYMIV;

    机译:基因分型分子标记Vignas MYMIV;

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