A Gain-of-Function Mutation in TRPA1 Causes familial episodic pain syndrome

ABSTRACT: Human monogenic pain syndromes have provided important insights into the molecular mechanisms that underlie normal and pathological pain states. We describe an autosomal-dominant familial episodic pain syndrome characterized by episodes of debilitating upper body pain, triggered by fasting...

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Autores:
Pineda Trujillo, Nicolás Guillermo
Bedoya Berrío, Gabriel de Jesús
Ruiz Linares, Andrés
Kremeyer, Barbara
Lopera Restrepo, Francisco Javier
Cox, James J.
Momin, Aliakmal
Rugiero, Francois
Marsh, Steve
Woods, C. Geoffrey
Jones, Nicholas G.
Paterson, Kathryn J.
Fricker, Florence R.
Villegas Lanau, Carlos Andrés
Acosta Baena, Natalia
Ramírez, Juan Diego
Zea, Julián
Burley, Mari Wyn
Bennett, David L.H.
Wood, John N.
Tipo de recurso:
Article of investigation
Fecha de publicación:
2010
Institución:
Universidad de Antioquia
Repositorio:
Repositorio UdeA
Idioma:
eng
OAI Identifier:
oai:bibliotecadigital.udea.edu.co:10495/33938
Acceso en línea:
https://hdl.handle.net/10495/33938
Palabra clave:
Análisis de Secuencia de Proteína
Sequence Analysis, Protein
Canales de Calcio
Calcium Channels
Línea Celular
Cell Line
Datos de Secuencia Molecular
Molecular Sequence Data
Rights
openAccess
License
https://creativecommons.org/licenses/by-nc-nd/2.5/co/
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oai_identifier_str oai:bibliotecadigital.udea.edu.co:10495/33938
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network_name_str Repositorio UdeA
repository_id_str
dc.title.spa.fl_str_mv A Gain-of-Function Mutation in TRPA1 Causes familial episodic pain syndrome
title A Gain-of-Function Mutation in TRPA1 Causes familial episodic pain syndrome
spellingShingle A Gain-of-Function Mutation in TRPA1 Causes familial episodic pain syndrome
Análisis de Secuencia de Proteína
Sequence Analysis, Protein
Canales de Calcio
Calcium Channels
Línea Celular
Cell Line
Datos de Secuencia Molecular
Molecular Sequence Data
title_short A Gain-of-Function Mutation in TRPA1 Causes familial episodic pain syndrome
title_full A Gain-of-Function Mutation in TRPA1 Causes familial episodic pain syndrome
title_fullStr A Gain-of-Function Mutation in TRPA1 Causes familial episodic pain syndrome
title_full_unstemmed A Gain-of-Function Mutation in TRPA1 Causes familial episodic pain syndrome
title_sort A Gain-of-Function Mutation in TRPA1 Causes familial episodic pain syndrome
dc.creator.fl_str_mv Pineda Trujillo, Nicolás Guillermo
Bedoya Berrío, Gabriel de Jesús
Ruiz Linares, Andrés
Kremeyer, Barbara
Lopera Restrepo, Francisco Javier
Cox, James J.
Momin, Aliakmal
Rugiero, Francois
Marsh, Steve
Woods, C. Geoffrey
Jones, Nicholas G.
Paterson, Kathryn J.
Fricker, Florence R.
Villegas Lanau, Carlos Andrés
Acosta Baena, Natalia
Ramírez, Juan Diego
Zea, Julián
Burley, Mari Wyn
Bennett, David L.H.
Wood, John N.
dc.contributor.author.none.fl_str_mv Pineda Trujillo, Nicolás Guillermo
Bedoya Berrío, Gabriel de Jesús
Ruiz Linares, Andrés
Kremeyer, Barbara
Lopera Restrepo, Francisco Javier
Cox, James J.
Momin, Aliakmal
Rugiero, Francois
Marsh, Steve
Woods, C. Geoffrey
Jones, Nicholas G.
Paterson, Kathryn J.
Fricker, Florence R.
Villegas Lanau, Carlos Andrés
Acosta Baena, Natalia
Ramírez, Juan Diego
Zea, Julián
Burley, Mari Wyn
Bennett, David L.H.
Wood, John N.
dc.contributor.researchgroup.spa.fl_str_mv Genética Molecular (GENMOL)
Grupo de Neurociencias de Antioquia
dc.subject.decs.none.fl_str_mv Análisis de Secuencia de Proteína
Sequence Analysis, Protein
Canales de Calcio
Calcium Channels
Línea Celular
Cell Line
Datos de Secuencia Molecular
Molecular Sequence Data
topic Análisis de Secuencia de Proteína
Sequence Analysis, Protein
Canales de Calcio
Calcium Channels
Línea Celular
Cell Line
Datos de Secuencia Molecular
Molecular Sequence Data
description ABSTRACT: Human monogenic pain syndromes have provided important insights into the molecular mechanisms that underlie normal and pathological pain states. We describe an autosomal-dominant familial episodic pain syndrome characterized by episodes of debilitating upper body pain, triggered by fasting and physical stress. Linkage and haplotype analysis mapped this phenotype to a 25 cM region on chromosome 8q12–8q13. Candidate gene sequencing identified a point mutation (N855S) in the S4 transmembrane segment of TRPA1, a key sensor for environmental irritants. The mutant channel showed a normal pharmacological profile but altered biophysical properties, with a 5-fold increase in inward current on activation at normal resting potentials. Quantitative sensory testing demonstrated normal baseline sensory thresholds but an enhanced secondary hyperalgesia to punctate stimuli on treatment with mustard oil. TRPA1 antagonists inhibit the mutant channel, promising a useful therapy for this disorder. Our findings provide evidence that variation in the TRPA1 gene can alter pain perception in humans.
publishDate 2010
dc.date.issued.none.fl_str_mv 2010
dc.date.accessioned.none.fl_str_mv 2023-03-12T19:25:34Z
dc.date.available.none.fl_str_mv 2023-03-12T19:25:34Z
dc.type.spa.fl_str_mv Artículo de investigación
dc.type.coar.spa.fl_str_mv http://purl.org/coar/resource_type/c_2df8fbb1
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dc.identifier.citation.spa.fl_str_mv Kremeyer B, Lopera F, Cox JJ, Momin A, Rugiero F, Marsh S, Woods CG, Jones NG, Paterson KJ, Fricker FR, Villegas A, Acosta N, Pineda-Trujillo NG, Ramírez JD, Zea J, Burley MW, Bedoya G, Bennett DL, Wood JN, Ruiz-Linares A. A gain-of-function mutation in TRPA1 causes familial episodic pain syndrome. Neuron. 2010 Jun 10;66(5):671-80. doi: 10.1016/j.neuron.2010.04.030.
dc.identifier.issn.none.fl_str_mv 0896-6273
dc.identifier.uri.none.fl_str_mv https://hdl.handle.net/10495/33938
dc.identifier.doi.none.fl_str_mv 10.1016/j.neuron.2010.04.030
dc.identifier.eissn.none.fl_str_mv 1097-4199
identifier_str_mv Kremeyer B, Lopera F, Cox JJ, Momin A, Rugiero F, Marsh S, Woods CG, Jones NG, Paterson KJ, Fricker FR, Villegas A, Acosta N, Pineda-Trujillo NG, Ramírez JD, Zea J, Burley MW, Bedoya G, Bennett DL, Wood JN, Ruiz-Linares A. A gain-of-function mutation in TRPA1 causes familial episodic pain syndrome. Neuron. 2010 Jun 10;66(5):671-80. doi: 10.1016/j.neuron.2010.04.030.
0896-6273
10.1016/j.neuron.2010.04.030
1097-4199
url https://hdl.handle.net/10495/33938
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.ispartofjournalabbrev.spa.fl_str_mv Neuron
dc.relation.citationendpage.spa.fl_str_mv 680
dc.relation.citationissue.spa.fl_str_mv 5
dc.relation.citationstartpage.spa.fl_str_mv 671
dc.relation.citationvolume.spa.fl_str_mv 66
dc.relation.ispartofjournal.spa.fl_str_mv Neuron
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dc.publisher.place.spa.fl_str_mv Cambridge, Estados Unidos
institution Universidad de Antioquia
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spelling Pineda Trujillo, Nicolás GuillermoBedoya Berrío, Gabriel de JesúsRuiz Linares, AndrésKremeyer, BarbaraLopera Restrepo, Francisco JavierCox, James J.Momin, AliakmalRugiero, FrancoisMarsh, SteveWoods, C. GeoffreyJones, Nicholas G.Paterson, Kathryn J.Fricker, Florence R.Villegas Lanau, Carlos AndrésAcosta Baena, NataliaRamírez, Juan DiegoZea, JuliánBurley, Mari WynBennett, David L.H.Wood, John N.Genética Molecular (GENMOL)Grupo de Neurociencias de Antioquia2023-03-12T19:25:34Z2023-03-12T19:25:34Z2010Kremeyer B, Lopera F, Cox JJ, Momin A, Rugiero F, Marsh S, Woods CG, Jones NG, Paterson KJ, Fricker FR, Villegas A, Acosta N, Pineda-Trujillo NG, Ramírez JD, Zea J, Burley MW, Bedoya G, Bennett DL, Wood JN, Ruiz-Linares A. A gain-of-function mutation in TRPA1 causes familial episodic pain syndrome. Neuron. 2010 Jun 10;66(5):671-80. doi: 10.1016/j.neuron.2010.04.030.0896-6273https://hdl.handle.net/10495/3393810.1016/j.neuron.2010.04.0301097-4199ABSTRACT: Human monogenic pain syndromes have provided important insights into the molecular mechanisms that underlie normal and pathological pain states. We describe an autosomal-dominant familial episodic pain syndrome characterized by episodes of debilitating upper body pain, triggered by fasting and physical stress. Linkage and haplotype analysis mapped this phenotype to a 25 cM region on chromosome 8q12–8q13. Candidate gene sequencing identified a point mutation (N855S) in the S4 transmembrane segment of TRPA1, a key sensor for environmental irritants. The mutant channel showed a normal pharmacological profile but altered biophysical properties, with a 5-fold increase in inward current on activation at normal resting potentials. Quantitative sensory testing demonstrated normal baseline sensory thresholds but an enhanced secondary hyperalgesia to punctate stimuli on treatment with mustard oil. TRPA1 antagonists inhibit the mutant channel, promising a useful therapy for this disorder. Our findings provide evidence that variation in the TRPA1 gene can alter pain perception in humans.COL0006723COL001074410application/pdfengCell PressCambridge, Estados Unidoshttps://creativecommons.org/licenses/by-nc-nd/2.5/co/https://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccesshttp://purl.org/coar/access_right/c_abf2A Gain-of-Function Mutation in TRPA1 Causes familial episodic pain syndromeArtículo de investigaciónhttp://purl.org/coar/resource_type/c_2df8fbb1https://purl.org/redcol/resource_type/ARThttp://purl.org/coar/version/c_970fb48d4fbd8a85info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionAnálisis de Secuencia de ProteínaSequence Analysis, ProteinCanales de CalcioCalcium ChannelsLínea CelularCell LineDatos de Secuencia MolecularMolecular Sequence DataNeuron680567166NeuronPublicationORIGINALPinedaNicolas_2010_FunctionMutationTRPA1.pdfPinedaNicolas_2010_FunctionMutationTRPA1.pdfArtículo de investigaciónapplication/pdf1199548https://bibliotecadigital.udea.edu.co/bitstreams/23fd1e0e-b10c-4765-bc25-d0161e79c4fa/download8a5e1dda9a2fd0ec5e52ca42dd06907eMD51trueAnonymousREADCC-LICENSElicense_rdflicense_rdfapplication/rdf+xml; charset=utf-8927https://bibliotecadigital.udea.edu.co/bitstreams/d3dc3cd0-6f91-4217-b3ba-73e6f24d4a6f/download1646d1f6b96dbbbc38035efc9239ac9cMD52falseAnonymousREADLICENSElicense.txtlicense.txttext/plain; charset=utf-81748https://bibliotecadigital.udea.edu.co/bitstreams/cb41b5b8-8762-4750-a725-7127b4bfaeba/download8a4605be74aa9ea9d79846c1fba20a33MD53falseAnonymousREADTEXTPinedaNicolas_2010_FunctionMutationTRPA1.pdf.txtPinedaNicolas_2010_FunctionMutationTRPA1.pdf.txtExtracted texttext/plain53744https://bibliotecadigital.udea.edu.co/bitstreams/000b3a5f-367d-4bd7-9d09-bf6bbc683d02/download5153e0bff974cdaddc0532281b14a520MD54falseAnonymousREADTHUMBNAILPinedaNicolas_2010_FunctionMutationTRPA1.pdf.jpgPinedaNicolas_2010_FunctionMutationTRPA1.pdf.jpgGenerated Thumbnailimage/jpeg17417https://bibliotecadigital.udea.edu.co/bitstreams/b08a5f7b-c461-4bac-9bdb-8f5901f34080/download77f754e1d6e61644b30e555baf52deabMD55falseAnonymousREAD10495/33938oai:bibliotecadigital.udea.edu.co:10495/339382025-03-26 19:48:08.19https://creativecommons.org/licenses/by-nc-nd/2.5/co/open.accesshttps://bibliotecadigital.udea.edu.coRepositorio Institucional de la Universidad de Antioquiaaplicacionbibliotecadigitalbiblioteca@udea.edu.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