Improving plant transient expression through the rational design of synthetic 5' and 3' untranslated regions

• Published in: Plant methods Vol. 15; no. 1; p. 108
• Main Authors: Peyret, Hadrien, Brown, James K M, Lomonossoff, George P
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 18-09-2019; BioMed Central; BMC
• Subjects: 3' Untranslated regions; Biochemistry; Botanical research; Cloning; Cowpea; Cowpeas; Deconstructed vectors; Design; Enhancers; Enzymes; Expression vectors; Gene expression; Genes; Genetic aspects; Genetic engineering; Genetic research; Industrial applications; Industrial equipment; Modulators; Molecular farming; Mutation; Novels; pEAQ; pHRE; pHREAC; Plant genetic engineering; Plant genetics; Plant transient expression; Plant viruses; Proteins; Recombinant proteins; Regulatory sequences; Ribonucleic acid; RNA; RNA viruses; Synthetic biology; Viruses; United Kingdom; United Kingdom > UK; Molecular farming; UTR; Deconstructed vectors; Viral expression system; pEAQ; pHREAC; Plant transient expression; Synthetic biology; Recombinant protein; pHRE
• ISSN: 1746-4811; 1746-4811
• DOI: 10.1186/s13007-019-0494-9

The growing field of plant molecular farming relies on expression vectors that allow high yields of recombinant proteins to be produced through transient gene expression. While numerous expression vectors currently exist for this purpose, there are very few examples of systematic efforts to improve upon these. Moreover, the current generation of expression systems makes use of naturally-occurring regulatory elements, typically selected from plant viruses, to maximise yields. This study aims to use rational design to generate synthetic sequences that can rival existing ones.
In this work, we present the rational design of novel synthetic 5' and 3' untranslated regions (UTRs) which can be used in various combinations to modulate accumulation levels of transiently-expressed recombinant proteins. Using the pEAQ-
expression vector as a point of comparison, we show that pre-existing expression systems can be improved by the deployment of rationally designed synthetic UTRs. Notably, we show that a suite of short, synthetic 5'UTRs behave as expression enhancers that outperform the
5'UTR present in the CPMV-
expression system. Furthermore, we confirm the critical role played by the 3'UTR of cowpea mosaic virus RNA-2 in the performance of the CPMV-
system. Finally, we use the knowledge obtained from these results to develop novel expression vectors (named pHRE and pHREAC) that equal or outperform pEAQ-
in terms of recombinant protein yield. These new vectors are also domesticated for the use of certain Type IIS restriction enzymes, which allows for quicker cloning and straightforward assessment of different combinations of UTRs.
We have shown that it is possible to rationally design a suite of expression modulators in the form of synthetic UTRs. We have created novel expression vectors that allow very high levels of recombinant protein expression in a transient expression context. This will have important consequences for future efforts to develop ever-better plant transient overexpression vectors for research or industrial applications.