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TmPrime: fast flexible oligonucleotide design software for gene synthesis

机译:TmPrime:用于基因合成的快速灵活的寡核苷酸设计软件

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摘要

Herein we present TmPrime, a computer program to design oligonucleotide sets for gene assembly by both ligase chain reaction (LCR) and polymerase chain reaction (PCR). TmPrime offers much flexibility with no constraints on the gene and oligonucleotide lengths. The program divides the long input DNA sequence based on the input desired melting temperature, and dynamically optimizes the length of oligonucleotides to achieve homologous melting temperatures. The output reports the melting temperatures, oligonucleotide sequences and potential formation of secondary structures. Our program also provides functions on sequence pooling to separate long genes into smaller pieces for multi-pool assembly and codon optimization for expression. The software has been successfully used in the design and synthesis of green fluorescent protein fragment (GFPuv) (760 bp), human protein kinase B-2 (PKB2) (1446 bp) and the promoter of human calcium-binding protein A4 (S100A4) (752 bp) using real-time PCR assembly with LCGreen I, which offers a novel approach to compare the efficiency of gene synthesis. The purity of assembled products is successfully estimated with the use of melting curve analysis, which would potentially eliminate the necessity for agarose gel electrophoresis. This program is freely available at .
机译:在这里,我们介绍TmPrime,这是一种计算机程序,可通过连接酶链反应(LCR)和聚合酶链反应(PCR)设计用于基因组装的寡核苷酸集。 TmPrime提供了很大的灵活性,而对基因和寡核苷酸的长度没有限制。该程序根据输入的所需熔解温度对长输入DNA序列进行划分,并动态优化寡核苷酸的长度以实现同源熔解温度。输出报告了解链温度,寡核苷酸序列和二级结构的潜在形成。我们的程序还提供序列合并功能,将长基因分离成较小的片段,以进行多池装配和密码子优化以表达。该软件已成功用于绿色荧光蛋白片段(GFPuv)(760 bp),人蛋白激酶B-2(PKB2)(1446 bp)和人钙结合蛋白A4(S100A4)启动子的设计和合成(752 bp)使用带有LCGreen I的实时PCR装配,提供了一种比较基因合成效率的新颖方法。通过使用熔解曲线分析成功地估计了组装产品的纯度,这可能消除了琼脂糖凝胶电泳的必要性。该程序可从以下网站免费获得。

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