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

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,...

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Autores principales: Plassais, Jocelyn, Lagoutte, Laetitia, Correard, Solenne, Paradis, Manon, Guaguère, Eric, Hédan, Benoit, Pommier, Alix, Botherel, Nadine, Cadiergues, Marie-Christine, Pilorge, Philippe, Silversides, David, Bizot, Maud, Samuels, Mark, Arnan, Carme, Johnson, Rory, Hitte, Christophe, Salbert, Gilles, Méreau, Agnès, Quignon, Pascale, Derrien, Thomas, André, Catherine
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5198995/
https://www.ncbi.nlm.nih.gov/pubmed/28033318
http://dx.doi.org/10.1371/journal.pgen.1006482
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author Plassais, Jocelyn
Lagoutte, Laetitia
Correard, Solenne
Paradis, Manon
Guaguère, Eric
Hédan, Benoit
Pommier, Alix
Botherel, Nadine
Cadiergues, Marie-Christine
Pilorge, Philippe
Silversides, David
Bizot, Maud
Samuels, Mark
Arnan, Carme
Johnson, Rory
Hitte, Christophe
Salbert, Gilles
Méreau, Agnès
Quignon, Pascale
Derrien, Thomas
André, Catherine
author_facet Plassais, Jocelyn
Lagoutte, Laetitia
Correard, Solenne
Paradis, Manon
Guaguère, Eric
Hédan, Benoit
Pommier, Alix
Botherel, Nadine
Cadiergues, Marie-Christine
Pilorge, Philippe
Silversides, David
Bizot, Maud
Samuels, Mark
Arnan, Carme
Johnson, Rory
Hitte, Christophe
Salbert, Gilles
Méreau, Agnès
Quignon, Pascale
Derrien, Thomas
André, Catherine
author_sort Plassais, Jocelyn
collection PubMed
description 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.
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spelling pubmed-51989952017-01-19 A Point Mutation in a lincRNA Upstream of GDNF Is Associated to a Canine Insensitivity to Pain: A Spontaneous Model for Human Sensory Neuropathies Plassais, Jocelyn Lagoutte, Laetitia Correard, Solenne Paradis, Manon Guaguère, Eric Hédan, Benoit Pommier, Alix Botherel, Nadine Cadiergues, Marie-Christine Pilorge, Philippe Silversides, David Bizot, Maud Samuels, Mark Arnan, Carme Johnson, Rory Hitte, Christophe Salbert, Gilles Méreau, Agnès Quignon, Pascale Derrien, Thomas André, Catherine PLoS Genet Research Article 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. Public Library of Science 2016-12-29 /pmc/articles/PMC5198995/ /pubmed/28033318 http://dx.doi.org/10.1371/journal.pgen.1006482 Text en © 2016 Plassais et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Plassais, Jocelyn
Lagoutte, Laetitia
Correard, Solenne
Paradis, Manon
Guaguère, Eric
Hédan, Benoit
Pommier, Alix
Botherel, Nadine
Cadiergues, Marie-Christine
Pilorge, Philippe
Silversides, David
Bizot, Maud
Samuels, Mark
Arnan, Carme
Johnson, Rory
Hitte, Christophe
Salbert, Gilles
Méreau, Agnès
Quignon, Pascale
Derrien, Thomas
André, Catherine
A Point Mutation in a lincRNA Upstream of GDNF Is Associated to a Canine Insensitivity to Pain: A Spontaneous Model for Human Sensory Neuropathies
title A Point Mutation in a lincRNA Upstream of GDNF Is Associated to a Canine Insensitivity to Pain: A Spontaneous Model for Human Sensory Neuropathies
title_full A Point Mutation in a lincRNA Upstream of GDNF Is Associated to a Canine Insensitivity to Pain: A Spontaneous Model for Human Sensory Neuropathies
title_fullStr A Point Mutation in a lincRNA Upstream of GDNF Is Associated to a Canine Insensitivity to Pain: A Spontaneous Model for Human Sensory Neuropathies
title_full_unstemmed A Point Mutation in a lincRNA Upstream of GDNF Is Associated to a Canine Insensitivity to Pain: A Spontaneous Model for Human Sensory Neuropathies
title_short A Point Mutation in a lincRNA Upstream of GDNF Is Associated to a Canine Insensitivity to Pain: A Spontaneous Model for Human Sensory Neuropathies
title_sort point mutation in a lincrna upstream of gdnf is associated to a canine insensitivity to pain: a spontaneous model for human sensory neuropathies
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5198995/
https://www.ncbi.nlm.nih.gov/pubmed/28033318
http://dx.doi.org/10.1371/journal.pgen.1006482
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