Evidence map›Paper›PMID 24705598›Full record

ArticleNature protocols2014

Design and construction of an in-plant activation cassette for transgene expression and recombinant protein production in plants.

Benjamin Dugdale, Cara L Mortimer, Maiko Kato, Tess A James, Robert M Harding, James L Dale

Abstract read
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In one paragraph

Article in Nature protocols, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
7.4field-weighted citation impact, top 3% 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

17 citing papers in PubMed, 40 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
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  5. Review
  6. Distinct domains of the AVRPM3The New phytologist · 2018
    Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Towards engineering carboxysomes into C3 plants.The Plant journal : for cell and molecular biology · 2016
    Article
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  14. Article
  15. Review
  16. Review
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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

6 authors at 1 institution in 1 country.

Benjamin Dugdale1] Centre for Tropical Crops and Biocommodities, Queensland University of Technology, Brisbane, Queensland, Australia. [2].
Cara L Mortimer1] Centre for Tropical Crops and Biocommodities, Queensland University of Technology, Brisbane, Queensland, Australia. [2].
Maiko KatoCentre for Tropical Crops and Biocommodities, Queensland University of Technology, Brisbane, Queensland, Australia.
Tess A JamesCentre for Tropical Crops and Biocommodities, Queensland University of Technology, Brisbane, Queensland, Australia.
Robert M HardingCentre for Tropical Crops and Biocommodities, Queensland University of Technology, Brisbane, Queensland, Australia.
James L DaleCentre for Tropical Crops and Biocommodities, Queensland University of Technology, Brisbane, Queensland, Australia.
Queensland University of Technology · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Virus-based transgene expression systems have become particularly valuable for recombinant protein production in plants. The dual-module in-plant activation (INPACT) expression platform consists of a uniquely designed split-gene cassette incorporating the cis replication elements of Tobacco yellow dwarf geminivirus (TYDV) and an ethanol-inducible activation cassette encoding the TYDV Rep and RepA replication-associated proteins. The INPACT system is essentially tailored for recombinant protein production in stably transformed plants and provides both inducible and high-level transient transgene expression with the potential to be adapted to diverse crop species. The construction of a novel split-gene cassette, the inducible nature of the system and the ability to amplify transgene expression via rolling-circle replication differentiates this system from other DNA- and RNA-based virus vector systems used for stable or transient recombinant protein production in plants. Here we provide a detailed protocol describing the design and construction of a split-gene INPACT cassette, and we highlight factors that may influence optimal activation and amplification of gene expression in transgenic plants. By using Nicotiana tabacum, the protocol takes 6-9 months to complete, and recombinant proteins expressed using INPACT can accumulate to up to 10% of the leaf total soluble protein.

Indexed as

EthanolGeminiviridaeGene Expression Regulation, PlantModels, GeneticNicotianaRecombinant ProteinsTranscriptional ActivationTransgenesEthanolRecombinant Proteins

Identifiers

PMID24705598
OpenAlexW1981436875

What OpenQuestion holds

Textmetadata
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.