Evidence map›Paper›PMID 41143712›Full record

ArticleACS synthetic biology2025

Boosting Gene Translation by a Short ORF Encoding for a "Nonsense" Peptide Positioned Immediately Upstream.

Junyi Cao, Sarah Goldberg, Roee Amit

Abstract read
In one paragraph

Article in ACS synthetic biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

3 authors.

Junyi CaoDepartment of Biotechnology and Food Engineering, Technion─Israel Institute of Technology, Haifa 32000, Israel.
Sarah GoldbergDepartment of Biotechnology and Food Engineering, Technion─Israel Institute of Technology, Haifa 32000, Israel.ORCID 0000-0003-1062-2084
Roee AmitDepartment of Biotechnology and Food Engineering, Technion─Israel Institute of Technology, Haifa 32000, Israel.ORCID 0000-0003-0580-7076

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We demonstrate a new synthetic genetic component for boosting translational levels in bacteria. Boosting is facilitated by a short and nonfunctional open reading frame (nfORF) that encodes a "nonsense" peptide located upstream of the target gene. The nfORF may be either in-frame or frame-shifted relative to the target open reading frame (tORF), and it contains an internal strong RBS that is immediately adjacent to its stop codon. We characterized 50 nfORFs, which allowed us to build a predictive model for the nfORF sequence, length, and distance from the tORF. Finally, we validated the model by testing three additional unseen nfORFs and demonstrated that the model also accurately predicts a translational boost for another target gene. Our results show how ribosome recruitment can be engineered to boost translation by as much as ×20 by precise engineering of an upstream nfORF. Our finding can be used for a variety of gene expression applications, by increasing expression for potentially any target gene that is produced in

Indexed as

Open Reading FramesPeptidesProtein BiosynthesisCodon, TerminatorEscherichia coliRibosomesCodon, TerminatorPeptidesexpression boostnonfunctional open reading frameribosomal stretchingtarget open reading frametranslational couplingtranslational reinitiation

Identifiers

PMID41143712
PMCPMC13255528

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.