Evidence map›Paper›PMID 37446368›Full record

ArticleInternational journal of molecular sciences2023

CRISPR/Cas9-Mediated Cytosine Base Editing Using an Improved Transformation Procedure in Melon (

Hadi Shirazi Parsa, Mohammad Sadegh Sabet, Ahmad Moieni, Abdolali Shojaeiyan, Catherine Dogimont, Adnane Boualem, Abdelhafid Bendahmane

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

12 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Uracil-DNA Glycosylase fromInternational journal of molecular sciences · 2025
    Article
  6. Review
  7. Article
  8. Unlocking the potential of 'Egusi' melon (Frontiers in plant science · 2025
    Review
  9. Article
  10. Article
  11. Article
  12. 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

7 authors at 3 institutions in 2 countries.

Hadi Shirazi ParsaUniversité Paris-Saclay, CNRS, INRAE, Université Evry, Institute of Plant Sciences Paris-Saclay (IPS2), 91190 Gif sur Yvette, France.ORCID 0009-0005-9785-8824
Mohammad Sadegh SabetDepartment of Plant Genetics and Breeding, Faculty of Agriculture, Tarbiat Modares University, Tehran 14115-336, Iran.
Ahmad MoieniDepartment of Plant Genetics and Breeding, Faculty of Agriculture, Tarbiat Modares University, Tehran 14115-336, Iran.
Abdolali ShojaeiyanDepartment of Horticulture, Faculty of Agriculture, Tarbiat Modares University, Tehran 14115-336, Iran.
Catherine DogimontINRAE, Génétique et Amélioration des Fruits et Légumes (GAFL), 84143 Montfavet, France.ORCID 0000-0001-7399-768X
Adnane BoualemUniversité Paris-Saclay, CNRS, INRAE, Université Evry, Institute of Plant Sciences Paris-Saclay (IPS2), 91190 Gif sur Yvette, France.
Abdelhafid BendahmaneUniversité Paris-Saclay, CNRS, INRAE, Université Evry, Institute of Plant Sciences Paris-Saclay (IPS2), 91190 Gif sur Yvette, France.ORCID 0000-0003-3246-868X
Centre National de la Recherche Scientifique · FRTarbiat Modares University · IRInstitut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement · FR

Funding

European Research Council 101095736
6 · The paper itself

Abstract

Melon is a recalcitrant plant for stable genetic transformation. Various protocols have been tried to improve melon transformation efficiency; however, it remains significantly low compared to other plants such as tomato. In this study, the primary focus was on the optimization of key parameters during the inoculation and co-culture steps of the genetic transformation protocol. Our results showed that immersing the explants in the inoculation medium for 20 min significantly enhanced transformation efficiency. During the co-culture step, the use of filer paper, 10 mM 2-(N-morpholino)-ethanesulfonic acid (MES), and a temperature of 24 °C significantly enhanced the melon transformation efficiency. Furthermore, the impact of different ethylene inhibitors and absorbers on the transformation efficiency of various melon varieties was explored. Our findings revealed that the use of these compounds led to a significant improvement in the transformation efficiency of the tested melon varieties. Subsequently, using our improved protocol and reporter-gene construct, diploid transgenic melons successfully generated. The efficiency of plant genetic transformation ranged from 3.73 to 4.83%. Expanding the scope of our investigation, the optimized protocol was applied to generate stable gene-edited melon lines using the Clustered regularly interspaced short palindromic repeats/CRISPR-associated protein 9 (CRISPR/Cas9)-mediated cytosine base editor and obtained melon lines with editions (C-to-T and C-to-G) in the eukaryotic translation initiation factor 4E,

Indexed as

Cucumis meloCucurbitaceaeCRISPR-Cas SystemsGene EditingPlantsCmeIF4E geneethylenegene editinggenetic transformation

Identifiers

PMID37446368
PMCPMC10342833
OpenAlexW4383551445

What OpenQuestion holds

Textmetadata
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.