Evidence map›Paper›PMID 28033318›Full record

ArticlePLoS genetics2016

A Point Mutation in a lincRNA Upstream of GDNF Is Associated to a Canine Insensitivity to Pain: A Spontaneous Model for Human Sensory Neuropathies.

Jocelyn Plassais, Laetitia Lagoutte, Solenne Correard, Manon Paradis, Eric Guaguère, Benoit Hédan, Alix Pommier, Nadine Botherel, Marie-Christine Cadiergues, Philippe Pilorge and 11 more

Abstract read
In one paragraph

Article in PLoS genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing 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

25 citing papers in PubMed.

  1. Article
  2. Whole exome sequencing as a screening tool in dogs: A pilot study.Computational and structural biotechnology journal · 2025
    Article
  3. Review
  4. The Shepherd and the Hunter: A Genomic Comparison of Italian Dog Breeds.Animals : an open access journal from MDPI · 2023
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Epigenetic Mechanisms in Canine Cancer.Frontiers in oncology · 2020
    Review
  14. Article
  15. Review
  16. Article
  17. Review
  18. Review
  19. Article
  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

21 authors.

Jocelyn PlassaisCNRS, UMR 6290, Institut de Génétique et Développement de Rennes, Rennes, France.
Laetitia LagoutteCNRS, UMR 6290, Institut de Génétique et Développement de Rennes, Rennes, France.
Solenne CorreardCNRS, UMR 6290, Institut de Génétique et Développement de Rennes, Rennes, France.
Manon ParadisDepartment of Clinical Sciences, Faculté de Médecine Vétérinaire, University of Montreal, Montreal, Québec, Canada.
Eric GuaguèreClinique Vétérinaire Saint Bernard, Lomme, France.
Benoit HédanCNRS, UMR 6290, Institut de Génétique et Développement de Rennes, Rennes, France.
Alix PommierCNRS, UMR 6290, Institut de Génétique et Développement de Rennes, Rennes, France.ORCID http://orcid.org/0000-0003-0588-8099
Nadine BotherelCNRS, UMR 6290, Institut de Génétique et Développement de Rennes, Rennes, France.
Marie-Christine CadierguesUDEAR, Université de Toulouse, Ecole Nationale Vétérinaire de Toulouse, INSERM, Toulouse, France.ORCID http://orcid.org/0000-0001-6909-0153
Philippe PilorgeClinique Vétérinaire de Saint-Cyr, Rennes, France.
David SilversidesDepartment of Clinical Sciences, Faculté de Médecine Vétérinaire, University of Montreal, Montreal, Québec, Canada.
Maud BizotCNRS, UMR 6290, Institut de Génétique et Développement de Rennes, Rennes, France.
Mark SamuelsDepartment of Biochemistry and Molecular Medicine, CHU Sainte-Justine, University of Montreal, Montreal, Québec, Canada.
Carme ArnanCentre for Genomic Regulation (CRG), Barcelona, Spain.ORCID http://orcid.org/0000-0002-7431-2088
Rory JohnsonCentre for Genomic Regulation (CRG), Barcelona, Spain.ORCID http://orcid.org/0000-0003-4607-2782
Christophe HitteCNRS, UMR 6290, Institut de Génétique et Développement de Rennes, Rennes, France.
Gilles SalbertCNRS, UMR 6290, Institut de Génétique et Développement de Rennes, Rennes, France.
Agnès MéreauCNRS, UMR 6290, Institut de Génétique et Développement de Rennes, Rennes, France.
Pascale QuignonCNRS, UMR 6290, Institut de Génétique et Développement de Rennes, Rennes, France.
Thomas DerrienCNRS, UMR 6290, Institut de Génétique et Développement de Rennes, Rennes, France.
Catherine AndréCNRS, UMR 6290, Institut de Génétique et Développement de Rennes, Rennes, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human Hereditary Sensory Autonomic Neuropathies (HSANs) are characterized by insensitivity to pain, sometimes combined with self-mutilation. Strikingly, several sporting dog breeds are particularly affected by such neuropathies. Clinical signs appear in young puppies and consist of acral analgesia, with or without sudden intense licking, biting and severe self-mutilation of the feet, whereas proprioception, motor abilities and spinal reflexes remain intact. Through a Genome Wide Association Study (GWAS) with 24 affected and 30 unaffected sporting dogs using the Canine HD 170K SNP array (Illumina), we identified a 1.8 Mb homozygous locus on canine chromosome 4 (adj. p-val = 2.5x10-6). Targeted high-throughput sequencing of this locus in 4 affected and 4 unaffected dogs identified 478 variants. Only one variant perfectly segregated with the expected recessive inheritance in 300 sporting dogs of known clinical status, while it was never present in 900 unaffected dogs from 130 other breeds. This variant, located 90 kb upstream of the GDNF gene, a highly relevant neurotrophic factor candidate gene, lies in a long intergenic non-coding RNAs (lincRNA), GDNF-AS. Using human comparative genomic analysis, we observed that the canine variant maps onto an enhancer element. Quantitative RT-PCR of dorsal root ganglia RNAs of affected dogs showed a significant decrease of both GDNF mRNA and GDNF-AS expression levels (respectively 60% and 80%), as compared to unaffected dogs. We thus performed gel shift assays (EMSA) that reveal that the canine variant significantly alters the binding of regulatory elements. Altogether, these results allowed the identification in dogs of GDNF as a relevant candidate for human HSAN and insensitivity to pain, but also shed light on the regulation of GDNF transcription. Finally, such results allow proposing these sporting dog breeds as natural models for clinical trials with a double benefit for human and veterinary medicine.

Indexed as

AnimalsChromosome MappingDogsGene Expression RegulationGenome-Wide Association StudyGlial Cell Line-Derived Neurotrophic FactorHereditary Sensory and Autonomic NeuropathiesHumansPainPain Insensitivity, CongenitalPoint MutationPolymorphism, Single NucleotideRNA, Long NoncodingGlial Cell Line-Derived Neurotrophic FactorRNA, Long Noncoding

Identifiers

PMID28033318
PMCPMC5198995

What OpenQuestion holds

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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.