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A Novel mRNA Level Subtraction Method for Quick Identification of Target-Orientated Uniquely Expressed Genes Between Peanut Immature Pod and Leaf

机译:一种新型的mRNA水平消减方法,用于快速鉴定花生未成熟荚果和叶片之间的目标定向独特表达基因

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Subtraction technique has been broadly applied for target gene discovery. However, most current protocols apply relative differential subtraction and result in great amount clone mixtures of unique and differentially expressed genes. This makes it more difficult to identify unique or target-orientated expressed genes. In this study, we developed a novel method for subtraction at mRNA level by integrating magnetic particle technology into driver preparation and tester–driver hybridization to facilitate uniquely expressed gene discovery between peanut immature pod and leaf through a single round subtraction. The resulting target clones were further validated through polymerase chain reaction screening using peanut immature pod and leaf cDNA libraries as templates. This study has resulted in identifying several genes expressed uniquely in immature peanut pod. These target genes can be used for future peanut functional genome and genetic engineering research.
机译:减法技术已广泛应用于靶基因发现。然而,大多数当前方案应用相对差异减法,并导致大量独特和差异表达基因的克隆混合物。这使得鉴定独特的或靶标定向的表达基因更加困难。在这项研究中,我们开发了一种在mRNA水平上扣除的新方法,该方法通过将磁性粒子技术整合到驱动程序制备和测试程序-驱动程序杂交中,以通过单轮扣除促进花生未成熟荚果和叶片之间独特表达的基因发现。通过聚合酶链反应筛选进一步验证得到的目标克隆,使用花生未成熟豆荚和叶片cDNA文库作为模板。这项研究导致鉴定了几个在未成熟花生荚中独特表达的基因。这些靶基因可用于未来的花生功能基因组和基因工程研究。

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