Evidence map›Paper›PMID 35639605›Full record

ArticlePlant biotechnology journal2022

A single promoter-TALE system for tissue-specific and tuneable expression of multiple genes in rice.

Florence Danila, Tom Schreiber, Maria Ermakova, Lei Hua, Daniela Vlad, Shuen-Fang Lo, Yi-Shih Chen, Julia Lambret-Frotte, Anna S Hermanns, Benedikt Athmer and 7 more

Open access · goldAbstract read
In one paragraph

Article in Plant biotechnology journal, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.6field-weighted citation impact, top 16% of its field
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

14 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
  2. The Promise of Synthetic Biology for Redesigning Plant Architecture.International journal of molecular sciences · 2026
    Review
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  6. Article
  7. Gibberellins: extending the Green Revolution.Journal of experimental botany · 2025
    Review
  8. The switch-liker's guide to plant synthetic gene circuits.The Plant journal : for cell and molecular biology · 2025
    Review
  9. Promoters, KeyInternational journal of molecular sciences · 2024
    Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. Review
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

17 authors at 6 institutions in 4 countries.

Florence DanilaAustralian Research Council Centre of Excellence for Translational Photosynthesis, Plant Sciences Division, Research School of Biology, Australian National University, Canberra, Australian Capital Territory, Australia.ORCID 0000-0002-7352-3852
Tom SchreiberDepartment of Cell and Metabolic Biology, Leibniz Institute of Plant Biochemistry, Halle, Germany.ORCID 0000-0001-5457-178X
Maria ErmakovaAustralian Research Council Centre of Excellence for Translational Photosynthesis, Plant Sciences Division, Research School of Biology, Australian National University, Canberra, Australian Capital Territory, Australia.ORCID 0000-0001-8466-4186
Lei HuaDepartment of Plant Sciences, University of Cambridge, Cambridge, UK.
Daniela VladDepartment of Plant Sciences, University of Oxford, Oxford, UK.
Shuen-Fang LoBiotechnology Center, National Chung Hsing University, Taichung, Taiwan.
Yi-Shih ChenInstitute of Molecular Biology, Academia Sinica, Taipei, Taiwan.
Julia Lambret-FrotteDepartment of Plant Sciences, University of Oxford, Oxford, UK.ORCID 0000-0002-5978-8475
Anna S HermannsDepartment of Plant Sciences, University of Oxford, Oxford, UK.
Benedikt AthmerDepartment of Cell and Metabolic Biology, Leibniz Institute of Plant Biochemistry, Halle, Germany.
Susanne von CaemmererAustralian Research Council Centre of Excellence for Translational Photosynthesis, Plant Sciences Division, Research School of Biology, Australian National University, Canberra, Australian Capital Territory, Australia.ORCID 0000-0002-8366-2071
Su-May YuBiotechnology Center, National Chung Hsing University, Taichung, Taiwan.
Julian M HibberdDepartment of Plant Sciences, University of Cambridge, Cambridge, UK.ORCID 0000-0003-0662-7958
Alain TissierDepartment of Cell and Metabolic Biology, Leibniz Institute of Plant Biochemistry, Halle, Germany.ORCID 0000-0002-9406-4245
Robert T FurbankAustralian Research Council Centre of Excellence for Translational Photosynthesis, Plant Sciences Division, Research School of Biology, Australian National University, Canberra, Australian Capital Territory, Australia.ORCID 0000-0001-8700-6613
Steven KellyDepartment of Plant Sciences, University of Oxford, Oxford, UK.ORCID 0000-0001-8583-5362
Jane A LangdaleDepartment of Plant Sciences, University of Oxford, Oxford, UK.ORCID 0000-0001-7648-3924
University of Oxford · GBAustralian National University · AULeibniz Institute of Plant Biochemistry · DENational Chung Hsing University · TWUniversity of Cambridge · GBInstitute of Molecular Biology, Academia Sinica · TW

Funding

Biotechnology and Biological Sciences Research Council BB/P003117/1
6 · The paper itself

Abstract

In biological discovery and engineering research, there is a need to spatially and/or temporally regulate transgene expression. However, the limited availability of promoter sequences that are uniquely active in specific tissue-types and/or at specific times often precludes co-expression of multiple transgenes in precisely controlled developmental contexts. Here, we developed a system for use in rice that comprises synthetic designer transcription activator-like effectors (dTALEs) and cognate synthetic TALE-activated promoters (STAPs). The system allows multiple transgenes to be expressed from different STAPs, with the spatial and temporal context determined by a single promoter that drives expression of the dTALE. We show that two different systems-dTALE1-STAP1 and dTALE2-STAP2-can activate STAP-driven reporter gene expression in stable transgenic rice lines, with transgene transcript levels dependent on both dTALE and STAP sequence identities. The relative strength of individual STAP sequences is consistent between dTALE1 and dTALE2 systems but differs between cell-types, requiring empirical evaluation in each case. dTALE expression leads to off-target activation of endogenous genes but the number of genes affected is substantially less than the number impacted by the somaclonal variation that occurs during the regeneration of transformed plants. With the potential to design fully orthogonal dTALEs for any genome of interest, the dTALE-STAP system thus provides a powerful approach to fine-tune the expression of multiple transgenes, and to simultaneously introduce different synthetic circuits into distinct developmental contexts.

Indexed as

OryzaGenes, ReporterPlantsPlants, Genetically ModifiedPromoter Regions, GeneticTransgenescell-type-specific gene expressiondTALE-STAPricesynthetic gene circuits

Identifiers

PMID35639605
PMCPMC9398400
OpenAlexW4282929715

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.