Dual UTR-A novel 5′ untranslated region design for synthetic biology applications

被引:16
作者
Le, Simone Balzer [1 ,2 ]
Onsager, Ingerid [3 ]
Lorentzen, Jon Andreas [1 ,4 ]
Lale, Rahmi [1 ]
机构
[1] Norwegian Univ Sci & Technol, Fac Nat Sci, Dept Biotechnol, PhotoSynLab, N-7491 Trondheim, Norway
[2] SINTEF Ind, Dept Biotechnol & Nanomed, N-7465 Trondheim, Norway
[3] Diatec Monoclonals, N-0349 Oslo, Norway
[4] Stavanger Univ Hosp, Dept Pathol, N-4011 Stavanger, Norway
关键词
5 ' untranslated region; transcription; translation; Escherichia coli; Pseudomonas putida; MESSENGER-RNA; GENE-EXPRESSION; TRANSLATION INITIATION; PM PROMOTER; TRANSCRIPTION; COLI; MUTAGENESIS; POLYMERASE; RIBOSOMES; SEQUENCES;
D O I
10.1093/synbio/ysaa006
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Bacterial 5' untranslated regions of mRNA (UTR) involve in a complex regulation of gene expression; however, the exact sequence features contributing to gene regulation are not yet fully understood. In this study, we report the design of a novel 5' UTR, dual UTR, utilizing the transcriptional and translational characteristics of 5' UTRs in a single expression cassette. The dual UTR consists of two 5' UTRs, each separately leading to either increase in transcription or translation of the reporter, that are separated by a spacer region, enabling de novo translation initiation. We rationally create dual UTRs with a wide range of expression profiles and demonstrate the functionality of the novel design concept in Escherichia coli and Pseudomonas putida using different promoter systems and coding sequences. Overall, we demonstrate the application potential of dual UTR design concept in various synthetic biology applications ranging from fine-tuning of gene expression to maximization of protein production.
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页数:11
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