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TRANCERs: engineering enhancers into autonomous tissue-specific expression cassettes

Abstract:

The process by which a foreign gene is introduced into a cell and translated into a functional protein is referred to as transgene expression. Understanding and optimising transgene expression is crucial for a wide variety of applications which range from investigating basic biology, synthetic biology, recombinant protein production to gene therapy. However, precise control over the timing and location of transgene expression remains a key limitation, particularly in therapeutic contexts where specificity and compactness are critical.

To address limitations of traditional promoter-based transgene construct approaches, we developed TRANCERs (TRanscriptionally Autonomous enhaNCERs), a modular and compact system that transforms cell type-specific enhancers into standalone sources of productive transcription. To accomplish this, we leveraged basic facets of enhancer function as well as known and novel principles of transcript stability and nuclear export.

We demonstrate that TRANCERs can drive lineage-restricted expression of both reporter and therapeutic genes across multiple mammalian cell types both in vitro and in vivo, and that this expression pattern faithfully mirrors the activity of the enhancer element used. Enhancer elements are the most cell type specific element in the mammalian genome and are used to drive development, differentiation and cellular responses to extrinsic signals. Therefore, the TRANCER system allows for the generation of specific stable expression constructs for all conceivable situations for which a native enhancer exists with the required activity pattern. Furthermore, we show that the TRANCER system is compatible with previously published machine learning derived artificial enhancer sequences suggesting the possibility even for specific bespoke expression patterns that do not exist in nature. This, combined with a significantly reduced vector footprint ideal for size-constrained delivery systems such as lentiviral vectors, means that the TRANCER system represent a significant step forward in our ability to control gene expression for both basic biology and therapeutic applications.

Publication status:
Published
Peer review status:
Not peer reviewed

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Preprint server copy:
10.1101/2025.10.27.684763

Authors

More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Radcliffe Department of Medicine
Sub department:
RDM-Weatherall Inst of Molecular Medicine
Oxford college:
Reuben College
Role:
Author
ORCID:
0009-0000-9472-9975
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Radcliffe Department of Medicine
Sub department:
RDM-Weatherall Inst of Molecular Medicine
Role:
Author
ORCID:
0000-0001-6330-1407
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
NDM
Sub department:
Oxford Ludwig Institute
Role:
Author
ORCID:
0000-0002-2963-6438
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Radcliffe Department of Medicine
Sub department:
RDM-Weatherall Inst of Molecular Medicine
Oxford college:
St Cross College
Role:
Author
ORCID:
0000-0003-1161-5409
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
NDM
Sub department:
Oxford Ludwig Institute
Role:
Author
ORCID:
0000-0001-9099-9169


More from this funder
Funder identifier:
https://ror.org/029chgv08
Grant:
225220/Z/22/Z
More from this funder
Funder identifier:
https://ror.org/03x94j517
Grant:
MC_UU_00016/14
MC_UU_00029/3


Preprint server:
bioRxiv
Publication date:
2025-10-27
DOI:


Language:
English
Pubs id:
2308321
UUID:
uuid_ce73b5e0-887f-40ce-956c-0ff1f20f379b
Local pid:
pubs:2308321
Source identifiers:
W4415652014
Deposit date:
2025-11-14
ARK identifier:

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