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首页> 外文期刊>Analytical Biochemistry: An International Journal of Analytical and Preparative Methods >An efficient approach for constructing shRNA expression vectors based on short oligonucleotide synthesis
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An efficient approach for constructing shRNA expression vectors based on short oligonucleotide synthesis

机译:基于短寡核苷酸合成构建shRNA表达载体的有效方法

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摘要

Traditional strategies for establishing shRNA expression constructs are inefficient, error-prone, or costly. We describe a simple approach that overcomes these drawbacks. Briefly, the sense and antisense strands of the short hairpin RNA coding sequence are segmented into two parts, respectively, at asymmetric sites. The four resulting short oligonucleotides are synthesized. Each oligonucleotide is annealed with its opposite, resulting in a double-stranded fragment with sticky termini at both ends. The two fragments so generated can be easily spliced by simple ligation to reconstitute the full-length short hairpin RNA coding sequence which can then be cloned into an appropriately restricted vector, (C) 2008 Elsevier Inc. All rights reserved.
机译:建立shRNA表达构建体的传统策略效率低下,容易出错或成本高昂。我们描述了一种克服这些缺点的简单方法。简而言之,短发夹RNA编码序列的有义和反义链分别在不对称位点分为两部分。合成了四个所得的短寡核苷酸。每种寡核苷酸均以相反的方式退火,从而产生在两端均带有粘性末端的双链片段。如此产生的两个片段可通过简单的连接容易地剪接以重构全长短发夹RNA编码序列,然后可将其克隆到适当限制的载体中,(C)2008 Elsevier Inc.。保留所有权利。

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