首页> 外文期刊>Theoretical and Applied Genetics: International Journal of Breeding Research and Cell Genetics >Development of SRAP, SNP and Multiplexed SCAR molecular markers for the major seed coat color gene in Brassica rapa L
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Development of SRAP, SNP and Multiplexed SCAR molecular markers for the major seed coat color gene in Brassica rapa L

机译:甘蓝型油菜主要种皮颜色基因SRAP,SNP和多重SCAR分子标记的开发

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摘要

Seed coat color inheritance in B. rapa was studied in F(1), F(2), F(3), and BC(1) progenies from a cross of a Canadian brown-seeded variety 'SPAN' and a Bangladeshi yellow sarson variety 'BARI-6'. A pollen effect was found when the yellow sarson line was used as the maternal parent. Seed coat color segregated into brown, yellow-brown and bright yellow classes. Segregation was under digenic control where the brown or yellow-brown color was dominant over bright yellow seed coat color. A sequence related amplified polymorphism (SRAP) marker linked closely to a major seed coat color gene (Br1/br1) was developed. This dominant SRAP molecular marker was successfully converted into single nucleotide polymorphism (SNP) markers and sequence characterized amplification region (SCAR) markers after the extended flanking sequence of the SRAP was obtained with chromosome walking. In total, 24 SNPs were identified with more than 2-kb sequence. A 12-bp deletion allowed the development of a SCAR marker linked closely to the Br1 gene. Using the five-fluorescence dye set supplied by ABI, four labeled M13 primers were integrated with different SCAR primers to increase the throughput of SCAR marker detection. Using multiplexed SCAR markers targeting insertions and deletions in a genome shows great potential for marker assisted selection in plant breeding.
机译:在F(1),F(2),F(3)和BC(1)子代中研究了B. rapa的种皮颜色遗传,该子代来自加拿大棕色种子品种“ SPAN”和孟加拉国黄色sarson的杂交品种“ BARI-6”。当黄色萨森线用作母本时,发现花粉效应。种皮的颜色分为棕色,黄棕色和亮黄色。分离是在双基因控制下进行的,其中棕色或黄棕色比明亮的黄色种皮颜色更占优势。开发了与主要种皮颜色基因(Br1 / br1)紧密相关的序列相关扩增多态性(SRAP)标记。通过染色体行走获得SRAP的延伸侧翼序列后,该优势SRAP分子标记已成功转换为单核苷酸多态性(SNP)标记和序列特征性扩增区域(SCAR)标记。总共鉴定出24个SNP,其序列超过2kb。 12 bp的删除允许发展与Br1基因紧密相连的SCAR标记。使用ABI提供的五种荧光染料组合,将四个标记的M13引物与不同的SCAR引物整合在一起,以提高SCAR标记检测的通量。使用针对基因组中的插入和缺失的多重SCAR标记,在植物育种中显示了标记辅助选择的巨大潜力。

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