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人参新栽培品种‘春蓬’的分子标记开发与主要乳状蛋白基因相关联。

Development of molecular markers for the determination of the new cultivar 'Chunpoong' in Panax ginseng C. A. Meyer associated with a major latex-like protein gene.

机构信息

Department of Oriental Medicinal Material & Processing, College of Life Science, Kyung Hee University, 1 Seocheondong, Giheung-gu, Yongin-si, Gyeonggi-do 446-701, South Korea.

出版信息

Biol Pharm Bull. 2010;33(2):183-7. doi: 10.1248/bpb.33.183.

Abstract

Chunpoong is one of the most valuable cultivars of Panax ginseng C. A. MEYER, and is widely grown in Korea and China. Insertion/deletion (InDel) markers and single nucleotide polymorphism (SNP) markers are useful tools for marker-assisted selections. The SNP marker for determinate Chunpoong was previously developed from the nad7 gene of mtDNA by Wang et al. (2009) but was effective only on a limited range of cultivars. In this study, we studied the reasons for this limited application and developed new useful markers for application in Chunpoong-breeding programs. The new markers of InDel and SNP were designed in the major latex-like protein (MLP-like) gene which was highly expressed in 4-year-old Chunpoong expressed sequence tags (ESTs). To validate the marker in polymerase chain reaction (PCR), we used an InDel marker for identification of Chunpoong in the 70 Panax samples based on a double-blind test, and the success rate was 100%. For rapid and reliable assay of Chunpoong in numerous samples, we utilized an EvaGreen dye and melting curve method on real-time PCR. Furthermore, we designed an SNP marker that depended on the InDel region for more efficient detection of Chunpoong in real-time PCR. Compared with PCR-based assays, our Chunpoong SNP marker and real-time PCR assay offers a significant savings of time and labor in the analysis of large numbers of Chunpoong samples.

摘要

春峰是人参(Panax ginseng C. A. Meyer)的一个极具价值的品种,在韩国和中国广泛种植。插入/缺失(InDel)标记和单核苷酸多态性(SNP)标记是用于标记辅助选择的有用工具。Wang 等人(2009 年)曾从 mtDNA 的 nad7 基因中开发出用于确定春峰的 SNP 标记,但仅在有限的品种范围内有效。在这项研究中,我们研究了这种应用受限的原因,并开发了新的有用标记,用于春峰的培育计划。新的 InDel 和 SNP 标记是在主要乳蛋白样(MLP-like)基因中设计的,该基因在 4 年生春峰的表达序列标签(EST)中高度表达。为了在聚合酶链反应(PCR)中验证标记,我们使用基于双盲测试的 InDel 标记鉴定了 70 个人参样本中的春峰,成功率为 100%。为了在大量样本中快速可靠地检测春峰,我们在实时 PCR 中使用了 EvaGreen 染料和熔解曲线法。此外,我们设计了一个 SNP 标记,该标记依赖于 InDel 区域,以便在实时 PCR 中更有效地检测春峰。与基于 PCR 的分析相比,我们的春峰 SNP 标记和实时 PCR 分析在分析大量春峰样本时节省了大量时间和劳动力。

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