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Generation and Characterization of SCARs by Cloning and Sequencing of RAPD Products: A Strategy for Species-specific Marker Development in Bamboo

机译:通过克隆和测序RAPD产品来生成和表征SCAR:竹子中特定物种标记开发的策略

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摘要

• Background and Aims The aim of this study was to develop species-specific molecular markers for Bambusa balcooa and B. tulda to allow for their proper identification, in order to avoid unintentional adulteration that affects the quality and quantity of paper pulp production.• Methods Two putative, species-specific RAPD markers, Bb836 for B. balcooa and Bt609 for B. tulda were generated using a PCR-based RAPD technique. Species-specificity of these two markers was confirmed through Southern hybridization in which RAPD gels were blotted and hybridized with radiolabelled cloned RAPD markers. Southern hybridization analyses were also performed to validate homology of the co-migrating Bb836 and Bt609 marker bands amplified from 16 different populations of B. balcooa and B. tulda, respectively. Sequence-characterized amplified region (SCAR) markers were developed from Bb836 and Bt609 sequences, using 20-mer oligonucleotide primers designed from both the flanking ends of the respective RAPD primers.• Key Results As anticipated, Bb836 hybridized with an amplified band from B. balcooa and Bt609 hybridized only with an amplified product from B. tulda; the two markers did not hybridize with the amplified products of any of the other 14 bamboo species studied. The two pairs of SCAR primers amplified the target sequences only in the respective species. The species-specific SCAR fragments were named as ‘Balco836’ for B. balcooa and ‘Tuldo609’ for B. tulda. The species-specific ‘Balco836’ was amplified from the genomic DNA of 80 individuals of 16 populations of B. balcooa studied. Similarly, the presence of ‘Tuldo609’ was noted in all the 80 individuals representing 16 populations of B. tulda assessed. These SCAR fragments contained no obvious repetitive sequence beyond the primers.• Conclusion These two molecular markers are potentially useful for regulatory agencies to establish sovereign rights of the germplasms of B. balcooa and B. tulda. In addition, this is the first report of species-specific SCAR marker development in bamboo.
机译:•背景和目的这项研究的目的是开发Balbusa balcooa和B. tulda的物种特异性分子标记,以便对其进行正确鉴定,以避免对纸浆生产的质量和数量造成意外掺假。•方法使用基于PCR的RAPD技术生成了两个假定的物种特异性RAPD标记,即B. balcooa的Bb836和B. tulda的Bt609。通过Southern杂交证实了这两种标记的物种特异性,在该杂交中,RAPD凝胶被印迹并与放射性标记的克隆的RAPD标记杂交。还进行了Southern杂交分析以验证分别从B. balcooa和B. tulda的16个不同种群中扩增的共迁移Bb836和Bt609标记带的同源性。使用从各个RAPD引物的两个侧翼末端设计的20-mer寡核苷酸引物,从Bb836和Bt609序列中开发出了具有序列特征的扩增区域(SCAR)标记。 balcooa和Bt609仅与B. tulda的扩增产物杂交;这两个标记未与所研究的其他14个竹种的扩增产物杂交。两对SCAR引物仅在相应物种中扩增靶序列。物种特异性的SCAR片段被称为B. balcooa,名称为“ Balco836”,而被命名为B. tulda,名称为“ Tuldo609”。从研究的B. balcooa的16个种群的80个个体的基因组DNA中扩增出物种特异性的“ Balco836”。同样,在评估的16个图尔达人人群中,共有80个人表示存在“ Tuldo609”。这些SCAR片段除引物外没有明显的重复序列。•结论这两个分子标记可能对监管机构建立 B种质的主权有用。 balcooa B。图尔达。此外,这是关于竹子中特定物种SCAR标记发育的首次报道。

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