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A Genetic Basis for Mechanosensory Traits in Humans

In all vertebrates hearing and touch represent two distinct sensory systems that both rely on the transformation of mechanical force into electrical signals. There is an extensive literature describing single gene mutations in humans that cause hearing impairment, but there are essentially none for...

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Autores principales: Frenzel, Henning, Bohlender, Jörg, Pinsker, Katrin, Wohlleben, Bärbel, Tank, Jens, Lechner, Stefan G., Schiska, Daniela, Jaijo, Teresa, Rüschendorf, Franz, Saar, Kathrin, Jordan, Jens, Millán, José M., Gross, Manfred, Lewin, Gary R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3341339/
https://www.ncbi.nlm.nih.gov/pubmed/22563300
http://dx.doi.org/10.1371/journal.pbio.1001318
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author Frenzel, Henning
Bohlender, Jörg
Pinsker, Katrin
Wohlleben, Bärbel
Tank, Jens
Lechner, Stefan G.
Schiska, Daniela
Jaijo, Teresa
Rüschendorf, Franz
Saar, Kathrin
Jordan, Jens
Millán, José M.
Gross, Manfred
Lewin, Gary R.
author_facet Frenzel, Henning
Bohlender, Jörg
Pinsker, Katrin
Wohlleben, Bärbel
Tank, Jens
Lechner, Stefan G.
Schiska, Daniela
Jaijo, Teresa
Rüschendorf, Franz
Saar, Kathrin
Jordan, Jens
Millán, José M.
Gross, Manfred
Lewin, Gary R.
author_sort Frenzel, Henning
collection PubMed
description In all vertebrates hearing and touch represent two distinct sensory systems that both rely on the transformation of mechanical force into electrical signals. There is an extensive literature describing single gene mutations in humans that cause hearing impairment, but there are essentially none for touch. Here we first asked if touch sensitivity is a heritable trait and second whether there are common genes that influence different mechanosensory senses like hearing and touch in humans. Using a classical twin study design we demonstrate that touch sensitivity and touch acuity are highly heritable traits. Quantitative phenotypic measures of different mechanosensory systems revealed significant correlations between touch and hearing acuity in a healthy human population. Thus mutations in genes causing deafness genes could conceivably negatively influence touch sensitivity. In agreement with this hypothesis we found that a proportion of a cohort of congenitally deaf young adults display significantly impaired measures of touch sensitivity compared to controls. In contrast, blind individuals showed enhanced, not diminished touch acuity. Finally, by examining a cohort of patients with Usher syndrome, a genetically well-characterized deaf-blindness syndrome, we could show that recessive pathogenic mutations in the USH2A gene influence touch acuity. Control Usher syndrome cohorts lacking demonstrable pathogenic USH2A mutations showed no impairment in touch acuity. Our study thus provides comprehensive evidence that there are common genetic elements that contribute to touch and hearing and has identified one of these genes as USH2A.
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spelling pubmed-33413392012-05-04 A Genetic Basis for Mechanosensory Traits in Humans Frenzel, Henning Bohlender, Jörg Pinsker, Katrin Wohlleben, Bärbel Tank, Jens Lechner, Stefan G. Schiska, Daniela Jaijo, Teresa Rüschendorf, Franz Saar, Kathrin Jordan, Jens Millán, José M. Gross, Manfred Lewin, Gary R. PLoS Biol Research Article In all vertebrates hearing and touch represent two distinct sensory systems that both rely on the transformation of mechanical force into electrical signals. There is an extensive literature describing single gene mutations in humans that cause hearing impairment, but there are essentially none for touch. Here we first asked if touch sensitivity is a heritable trait and second whether there are common genes that influence different mechanosensory senses like hearing and touch in humans. Using a classical twin study design we demonstrate that touch sensitivity and touch acuity are highly heritable traits. Quantitative phenotypic measures of different mechanosensory systems revealed significant correlations between touch and hearing acuity in a healthy human population. Thus mutations in genes causing deafness genes could conceivably negatively influence touch sensitivity. In agreement with this hypothesis we found that a proportion of a cohort of congenitally deaf young adults display significantly impaired measures of touch sensitivity compared to controls. In contrast, blind individuals showed enhanced, not diminished touch acuity. Finally, by examining a cohort of patients with Usher syndrome, a genetically well-characterized deaf-blindness syndrome, we could show that recessive pathogenic mutations in the USH2A gene influence touch acuity. Control Usher syndrome cohorts lacking demonstrable pathogenic USH2A mutations showed no impairment in touch acuity. Our study thus provides comprehensive evidence that there are common genetic elements that contribute to touch and hearing and has identified one of these genes as USH2A. Public Library of Science 2012-05-01 /pmc/articles/PMC3341339/ /pubmed/22563300 http://dx.doi.org/10.1371/journal.pbio.1001318 Text en Frenzel 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Frenzel, Henning
Bohlender, Jörg
Pinsker, Katrin
Wohlleben, Bärbel
Tank, Jens
Lechner, Stefan G.
Schiska, Daniela
Jaijo, Teresa
Rüschendorf, Franz
Saar, Kathrin
Jordan, Jens
Millán, José M.
Gross, Manfred
Lewin, Gary R.
A Genetic Basis for Mechanosensory Traits in Humans
title A Genetic Basis for Mechanosensory Traits in Humans
title_full A Genetic Basis for Mechanosensory Traits in Humans
title_fullStr A Genetic Basis for Mechanosensory Traits in Humans
title_full_unstemmed A Genetic Basis for Mechanosensory Traits in Humans
title_short A Genetic Basis for Mechanosensory Traits in Humans
title_sort genetic basis for mechanosensory traits in humans
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3341339/
https://www.ncbi.nlm.nih.gov/pubmed/22563300
http://dx.doi.org/10.1371/journal.pbio.1001318
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