Evidence map›Paper›PMID 40758859›Full record

ArticleACS synthetic biology2025

Bioluminescence-Driven Optimization of Geminivirus-Based Vectors as Tools for Plant Biotechnology.

Elena Garcia-Perez, Victor Vazquez-Vilriales, Marta Vazquez-Vilar, Araceli G Castillo, Karen S Sarkisyan, Rosa Lozano-Duran, Eduardo R Bejarano, Diego Orzaez

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. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

2 citing papers in PubMed.

  1. Article
  2. Article
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

8 authors.

Elena Garcia-PerezInstituto de Biología Molecular y Celular de Plantas, CSIC-UPV, Valencia 46022, Spain.
Victor Vazquez-VilrialesInstituto de Biología Molecular y Celular de Plantas, CSIC-UPV, Valencia 46022, Spain.
Marta Vazquez-VilarInstituto de Biología Molecular y Celular de Plantas, CSIC-UPV, Valencia 46022, Spain.
Araceli G CastilloInstituto de Hortofruticultura Subtropical y Mediterranea 'La Mayora', Universidad de Málaga-Consejo Superior de Investigaciones Científicas (IHSM-UMA-CSIC), Universidad de Málaga, Málaga 29010, Spain.
Karen S SarkisyanInstitute of Clinical Sciences, Faculty of Medicine and Imperial College Centre for Synthetic Biology, Imperial College London, London SW7 2AZ, U.K.
Rosa Lozano-DuranCentre for Plant Molecular Biology (ZMBP), Eberhard Karls University, Tübingen 72076, Germany.
Eduardo R BejaranoInstituto de Hortofruticultura Subtropical y Mediterranea 'La Mayora', Universidad de Málaga-Consejo Superior de Investigaciones Científicas (IHSM-UMA-CSIC), Universidad de Málaga, Málaga 29010, Spain.
Diego OrzaezInstituto de Biología Molecular y Celular de Plantas, CSIC-UPV, Valencia 46022, Spain.ORCID 0000-0003-1662-5403

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Viral replicons are valuable tools in plant biotechnology, widely utilized to increase recombinant protein production. Their ability to amplify gene dosage in a trigger-dependent manner also opens doors to regulatory applications. This work focuses on optimizing geminivirus-based vectors for Synthetic Biology applications in plants, using autobioluminescence as a sensitive, real-time reporter to characterize gene expression. Specifically, geminivirus-based synthetic replicons derived from bean yellow dwarf virus (BeYDV), tomato yellow leaf curl virus (TYLCV), and beet curly top virus (BCTV) were engineered and assessed for basal expression, inducibility, and recombinant protein coexpression potential. Our study provided insights into the strengths and limitations of each geminiviral replicon. BeYDV replicon displayed a robust activation profile suitable for complex tasks such as multigene expression, while TYLCV showed high expression levels despite moderate basal leakage. In contrast, BCTV demonstrated less favorable control and expression levels. Through a bioluminescence-based screening, the TYLCV system was further optimized to improve regulatory precision. These findings highlight the versatility of geminivirus replicons, paving the way for future engineering of synthetic gene circuits in plants.

Indexed as

BiotechnologyGeminiviridaeGenetic VectorsBegomovirusLuminescent MeasurementsPlants, Genetically ModifiedRecombinant ProteinsRepliconSynthetic BiologyRecombinant ProteinsBCTVBeYDVbioluminescencegeminivirusNicotiana benthamianaplant synthetic biologyTYLCV

Identifiers

PMID40758859
PMCPMC12362603

What OpenQuestion holds

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Registered trials

None linked

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.