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首页> 外文期刊>Journal of computational biology: A journal of computational molecular cell biology >A Novel Method to Predict Highly Expressed Genes Based on Radius Clustering and Relative Synonymous Codon Usage
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A Novel Method to Predict Highly Expressed Genes Based on Radius Clustering and Relative Synonymous Codon Usage

机译:基于半径聚类和相对同义密码子使用的高表达基因预测新方法

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Recombinant proteins play an important role in many aspects of life and have generated a huge income, notably in the industrial enzyme business. A gene is introduced into a vector and expressed in a host organismfor example, E. colito obtain a high productivity of target protein. However, transferred genes from particular organisms are not usually compatible with the host's expression system because of various reasons, for example, codon usage bias, GC content, repetitive sequences, and secondary structure. The solution is developing programs to optimize for designing a nucleotide sequence whose origin is from peptide sequences using properties of highly expressed genes (HEGs) of the host organism. Existing data of HEGs determined by practical and computer-based methods do not satisfy for qualifying and quantifying. Therefore, the demand for developing a new HEG prediction method is critical. We proposed a new method for predicting HEGs and criteria to evaluate gene optimization. Codon usage bias was weighted by amplifying the difference between HEGs and non-highly expressed genes (non-HEGs). The number of predicted HEGs is 5% of the genome. In comparison with Puigb's method, the result is twice as good as Puigb's one, in kernel ratio and kernel sensitivity. Concerning transcription/translation factor proteins (TF), the proposed method gives low TF sensitivity, while Puigb's method gives moderate one. In summary, the results indicated that the proposed method can be a good optional applying method to predict optimized genes for particular organisms, and we generated an HEG database for further researches in gene design (Supplementary Material).
机译:重组蛋白在生活的许多方面都起着重要作用,并且产生了可观的收入,特别是在工业酶领域。将基因导入载体并在宿主生物例如大肠杆菌中表达以获得高生产率的靶蛋白。但是,由于各种原因,例如,密码子使用偏倚,GC含量,重复序列和二级结构,从特定生物体转移的基因通常与宿主的表达系统不兼容。该解决方案正在开发程序,以利用宿主生物的高表达基因(HEG)的特性优化设计核苷酸序列,该核苷酸序列源自肽序列。通过实用和基于计算机的方法确定的HEG的现有数据无法满足定性和定量要求。因此,开发新的HEG预测方法的需求至关重要。我们提出了一种预测HEG的新方法和评估基因优化的标准。通过放大HEG与非高度表达基因(non-HEG)之间的差异来加权密码子使用偏倚。预测的HEG数量为基因组的5%。与Puibb方法相比,结果在核比例和核敏感性方面是Puibb方法的两倍。关于转录/翻译因子蛋白(TF),该方法对TF的敏感性较低,而Puigb法则为中等。总而言之,结果表明,该方法可以作为预测特定生物优化基因的很好的可选应用方法,并且我们生成了一个HEG数据库用于基因设计的进一步研究(补充材料)。

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