Skip to main content
Log in

Development of new binary expression systems for plant synthetic biology

  • Original Article
  • Published:
Plant Cell Reports Aims and scope Submit manuscript

Abstract

Key message

A novel plant binary expression system was developed from the compactin biosynthetic pathway 27 of Penicillium citrinum ML-236B. The system achieved >fivefold activation of gene expression in 28 transgenic tobacco.

Abstract

A diverse and well-characterized genetic toolset is fundamental to achieve the overall goals of plant synthetic biology. To properly coordinate expression of a multigene pathway, this toolset should include binary systems that control gene expression at the level of transcription. In plants, few highly functional, orthogonal transcriptional regulators have been identified. Here, we describe the process of developing synthetic plant transcription factors using regulatory elements from the Penicillium citrinum ML-236B (compactin) pathway. This pathway contains several genes including mlcA and mlcC that are transcriptionally regulated in a dose-dependent manner by the activator mlcR. In Nicotiana benthamiana, we first expressed mlcR with several cognate synthetic promoters driving expression of GFP. Synthetic promoters contained operator sequences from the compactin gene cluster. Following identification of the most active synthetic promoter, the DNA-binding domain from mlcR was used to generate chimeric transcription factors containing variable activation domains, including QF from the Neurospora crassa Q-system. Activity was measured at both protein and RNA levels which correlated with an R2 value of 0.94. A synthetic transcription factor with a QF activation domain increased gene expression from its synthetic promoter up to sixfold in N. benthamiana. Two systems were characterized in transgenic tobacco plants. The QF-based plants maintained high expression in tobacco, increasing expression from the cognate synthetic promoter by fivefold. Transgenic plants and non-transgenic plants were morphologically indistinguishable. The framework of this study can easily be adopted for other putative transcription factors to continue improvement of the plant synthetic biology toolbox.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4

Similar content being viewed by others

Data availability

The datasets generated during and/or analysed during the current study are available from the corresponding author on reasonable request.

Abbreviations

AD:

Activation domain

DBD:

DNA-binding domain

LBD:

Ligand-binding domain

UAS:

Upstream activation sequence

TF:

Transcription factor

References

Download references

Funding

The authors acknowledge funding by the Defense Advanced Research Projects Agency (Award No. HR0011-18-2-0049) and USDA Hatch grants to CNS and SCL.

Author information

Authors and Affiliations

Authors

Contributions

ACP, CNS, and SCL designed the strategy. ACP, DNR, MC, SAH, and TMS collected data. ACP, DNR, MC, TMS, and SCL analyzed data. ACP, CNS, and SCL wrote the article.

Corresponding author

Correspondence to Scott C. Lenaghan.

Ethics declarations

Conflict of interest

The authors declare no competing interests.

Additional information

Communicated by Wei Ma.

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

The views, opinions, and/or findings expressed are those of the authors and should not be interpreted as representing the official views of policies of the Department of Defense or the United States Government (Approved for Public Release, Distribution Unlimited).

Supplementary Information

Below is the link to the electronic supplementary material.

Supplementary file1 (XLSX 14 KB)

Supplementary file2 (DOCX 98 KB)

Rights and permissions

Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Pfotenhauer, A.C., Reuter, D.N., Clark, M. et al. Development of new binary expression systems for plant synthetic biology. Plant Cell Rep 43, 22 (2024). https://doi.org/10.1007/s00299-023-03100-y

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1007/s00299-023-03100-y

Keywords

Navigation