Evidence map›Paper›PMID 27143231›Full record

ArticleNature communications2016

Highly efficient baculovirus-mediated multigene delivery in primary cells.

Maysam Mansouri, Itxaso Bellon-Echeverria, Aurélien Rizk, Zahra Ehsaei, Chiara Cianciolo Cosentino, Catarina S Silva, Ye Xie, Frederick M Boyce, M Wayne Davis, Stephan C F Neuhauss and 4 more

Abstract read
In one paragraph

Article in Nature communications, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing 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

59 citing papers in PubMed.

  1. Article
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  3. The design and engineering of synthetic genomes.Nature reviews. Genetics · 2025
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  9. Genome editing and kidney health.Clinical kidney journal · 2024
    Review
  10. Article
  11. Illuminating Neuropeptide Y YACS pharmacology & translational science · 2024
    Article
  12. Article
  13. Assembly of Baculovirus Vectors for Multiplexed Prime Editing.Methods in molecular biology (Clifton, N.J.) · 2024
    Article
  14. Baculovirus Production and Infection in Axolotls.Methods in molecular biology (Clifton, N.J.) · 2023
    Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Review
  20. 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

14 authors.

Maysam MansouriBiomolecular Research, Molecular Cell Biology, Paul Scherrer Institute, CH-5232 Villigen, Switzerland.
Itxaso Bellon-EcheverriaEuropean Molecular Biology Laboratory (EMBL), Grenoble Outstation, B.P. 181, 38042 Grenoble Cedex 9, France.
Aurélien RizkBiomolecular Research, Molecular Cell Biology, Paul Scherrer Institute, CH-5232 Villigen, Switzerland.
Zahra EhsaeiDepartment of Biomedicine, University of Basel, CH-4058 Basel, Switzerland.
Chiara Cianciolo CosentinoInstitute of Molecular Life Sciences, University of Zürich, CH-8057 Zürich, Switzerland.
Catarina S SilvaEuropean Molecular Biology Laboratory (EMBL), Grenoble Outstation, B.P. 181, 38042 Grenoble Cedex 9, France.
Ye XieBiomolecular Research, Molecular Cell Biology, Paul Scherrer Institute, CH-5232 Villigen, Switzerland.
Frederick M BoyceDepartment of Neurology, Massachusetts General Hospital, Cambridge, Massachusetts 02139, USA.
M Wayne DavisDepartment of Biology and Howard Hughes Medical Institute, University of Utah, Salt Lake City, Utah 84112-0840, USA.
Stephan C F NeuhaussInstitute of Molecular Life Sciences, University of Zürich, CH-8057 Zürich, Switzerland.
Verdon TaylorDepartment of Biomedicine, University of Basel, CH-4058 Basel, Switzerland.
Kurt Ballmer-HoferBiomolecular Research, Molecular Cell Biology, Paul Scherrer Institute, CH-5232 Villigen, Switzerland.
Imre BergerEuropean Molecular Biology Laboratory (EMBL), Grenoble Outstation, B.P. 181, 38042 Grenoble Cedex 9, France.
Philipp BergerBiomolecular Research, Molecular Cell Biology, Paul Scherrer Institute, CH-5232 Villigen, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multigene delivery and subsequent cellular expression is emerging as a key technology required in diverse research fields including, synthetic and structural biology, cellular reprogramming and functional pharmaceutical screening. Current viral delivery systems such as retro- and adenoviruses suffer from limited DNA cargo capacity, thus impeding unrestricted multigene expression. We developed MultiPrime, a modular, non-cytotoxic, non-integrating, baculovirus-based vector system expediting highly efficient transient multigene expression from a variety of promoters. MultiPrime viruses efficiently transduce a wide range of cell types, including non-dividing primary neurons and induced-pluripotent stem cells (iPS). We show that MultiPrime can be used for reprogramming, and for genome editing and engineering by CRISPR/Cas9. Moreover, we implemented dual-host-specific cassettes enabling multiprotein expression in insect and mammalian cells using a single reagent. Our experiments establish MultiPrime as a powerful and highly efficient tool, to deliver multiple genes for a wide range of applications in primary and established mammalian cells.

Indexed as

CRISPR-Cas SystemsGene Transfer TechniquesAnimalsBaculoviridaeCells, CulturedCellular Reprogramming TechniquesChlorocebus aethiopsCOS CellsGenetic VectorsHEK293 CellsHeLa CellsHumansSf9 CellsTransfectionTransgenes

Identifiers

PMID27143231
PMCPMC4857464

What OpenQuestion holds

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LicenceCC BY
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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.