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...
- 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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| 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 |
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http://purl.org/coar/resource_type/c_2df8fbb1 |
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https://purl.org/redcol/resource_type/ART |
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http://purl.org/coar/version/c_970fb48d4fbd8a85 |
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info:eu-repo/semantics/article |
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info:eu-repo/semantics/publishedVersion |
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http://purl.org/coar/resource_type/c_2df8fbb1 |
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publishedVersion |
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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 |
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680 |
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5 |
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671 |
| dc.relation.citationvolume.spa.fl_str_mv |
66 |
| dc.relation.ispartofjournal.spa.fl_str_mv |
Neuron |
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https://creativecommons.org/licenses/by-nc-nd/2.5/co/ |
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https://creativecommons.org/licenses/by-nc-nd/4.0/ |
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info:eu-repo/semantics/openAccess |
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openAccess |
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10 |
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Cell Press |
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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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 |
