Toward Predictable 5′UTRs in Saccharomyces cerevisiae: Development of a yUTR Calculator

被引:20
作者
Decoene, Thomas [1 ]
Peters, Gert [1 ]
De Maeseneire, Sofie L. [2 ]
De Mey, Marjan [1 ]
机构
[1] Univ Ghent, Ctr Synthet Biol, Coupure Links 653, B-9000 Ghent, Belgium
[2] Univ Ghent, Ctr Ind Biotechnol & Biocatalysis, Coupure Links 653, B-9000 Ghent, Belgium
来源
ACS SYNTHETIC BIOLOGY | 2018年 / 7卷 / 02期
关键词
translational fine-tuning; computational design; forward engineering; 5 ' UTR; Saccharomyces cerevisiae; OPEN READING FRAMES; GENE-EXPRESSION; MESSENGER-RNA; RIBOSOME BINDING; FLUORESCENT PROTEIN; CORE PROMOTERS; TRANSLATION; YEAST; CODON; SEQUENCES;
D O I
10.1021/acssynbio.7b00366
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Fine-tuning biosynthetic pathways is crucial for the development of economic feasible microbial cell factories. Therefore, the use of computational models able to predictably design regulatory sequences for pathway engineering proves to be a valuable tool, especially for modifying genes at the translational level. In this study we developed a computational approach for the de novo design of 5'-untranslated regions (5'UTRs) in Saccharomyces cerevisiae with a predictive outcome on translation initiation rate. On the basis of existing data, a partial least-squares (PLS) regression model was trained and showed good performance on predicting protein abundances of an independent test set. This model was further used for the construction of a "yUTR calculator" that can design 5'UTR sequences with a diverse range of desired translation efficiencies. The predictive power of our yUTR calculator was confirmed in vivo by different representative case studies. As such, these results show the great potential of data driven approaches for reliable pathway engineering in S. cerevisiae.
引用
收藏
页码:622 / 634
页数:25
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