Evidence map›Paper›PMID 24835852›Full record

ArticlePloS one2014

Development of a Cucumis sativus TILLinG platform for forward and reverse genetics.

Adnane Boualem, Sebastien Fleurier, Christelle Troadec, Pascal Audigier, Anish P K Kumar, Manash Chatterjee, Abdullah A Alsadon, Monther T Sadder, Mahmoud A Wahb-Allah, Abdullah A Al-Doss and 1 more

Abstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing 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

15 citing papers in PubMed.

  1. Review
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  8. Article
  9. Breeding science · 2018
    Article
  10. Review
  11. Article
  12. Article
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  15. 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

11 authors.

Adnane BoualemINRA-URGV, UMR1165, Unité de Recherche en Génomique Végétale, Saclay Plant Sciences, Evry, France.
Sebastien FleurierINRA-URGV, UMR1165, Unité de Recherche en Génomique Végétale, Saclay Plant Sciences, Evry, France.
Christelle TroadecINRA-URGV, UMR1165, Unité de Recherche en Génomique Végétale, Saclay Plant Sciences, Evry, France.
Pascal AudigierINRA-URGV, UMR1165, Unité de Recherche en Génomique Végétale, Saclay Plant Sciences, Evry, France.
Anish P K KumarBench Bio Pvt Ltd., c/o Jai Research Foundation, Vapi, Gujarat, India.
Manash ChatterjeeBench Bio Pvt Ltd., c/o Jai Research Foundation, Vapi, Gujarat, India; Plant and AgriBiosciences Research Centre (PABC), Botany and Plant Science, National University of Ireland Galway, University Road, Galway, Ireland.
Abdullah A AlsadonDepartment of Plant Production, College of Food and Agricultural Sciences, King Saud University, Riyadh, Saudi Arabia.
Monther T SadderDepartment of Plant Production, College of Food and Agricultural Sciences, King Saud University, Riyadh, Saudi Arabia.
Mahmoud A Wahb-AllahDepartment of Plant Production, College of Food and Agricultural Sciences, King Saud University, Riyadh, Saudi Arabia.
Abdullah A Al-DossDepartment of Plant Production, College of Food and Agricultural Sciences, King Saud University, Riyadh, Saudi Arabia.
Abdelhafid BendahmaneINRA-URGV, UMR1165, Unité de Recherche en Génomique Végétale, Saclay Plant Sciences, Evry, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCucumber (Cucumis sativus) belongs to the Cucurbitaceae family that includes more than 800 species. The cucumber genome has been recently sequenced and annotated. Transcriptomics and genome sequencing of many plant genomes are providing information on candidate genes potentially related to agronomically important traits. To accelerate functional characterization of these genes in cucumber we have generated an EMS mutant population that can be used as a TILLinG platform for reverse genetics. PRINCIPAL

findingsA population of 3,331 M2 mutant seed families was generated using two EMS concentrations (0.5% and 0.75%). Genomic DNA was extracted from M2 families and eight-fold pooled for mutation detection by ENDO1 nuclease. To assess the quality of the mutant collection, we screened for induced mutations in five genes and identified 26 mutations. The average mutation rate was calculated as 1/1147 Kb giving rise to approximately 320 mutations per genome. We focused our characterization on three missense mutations, G33C, S238F and S249F identified in the CsACS2 sex determination gene. Protein modeling and crystallography studies predicted that mutation at G33 may affect the protein function, whereas mutations at S238 and S249 may not impair the protein function. As predicted, detailed phenotypic evaluation showed that the S238F and the S249F mutant lines had no sexual phenotype. In contrast, plants homozygous for the G33C mutation showed a complete sexual transition from monoecy to andromonoecy. This result demonstrates that TILLinG is a valuable tool for functional validation of gene function in crops recalcitrant to transgenic transformation.

conclusionsWe have developed a cucumber mutant population that can be used as an efficient reverse genetics tool. The cucumber TILLinG collection as well as the previously described melon TILLinG collection will prove to be a valuable resource for both fundamental research and the identification of agronomically-important genes for crop improvement in cucurbits in general.

Indexed as

Mutation, MissenseAmino Acid SequenceCucumis sativusMolecular Sequence DataPhenotypePlant ProteinsReverse GeneticsPlant Proteins

Identifiers

PMID24835852
PMCPMC4024006

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Registered trials

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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.