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Human enamel thickness and ENAM polymorphism
The tooth enamel development gene, enamelin (ENAM), showed evidence of positive selection during a genome-wide scan of human and primate DNA for signs of adaptive evolution. The current study examined the hypothesis that a single-nucleotide polymorphism (SNP) C14625T (rs7671281) in the ENAM gene ide...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4932773/ https://www.ncbi.nlm.nih.gov/pubmed/27357321 http://dx.doi.org/10.1038/ijos.2016.1 |
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author | Daubert, Diane M Kelley, Joanna L Udod, Yuriy G Habor, Carolina Kleist, Chris G Furman, Ilona K Tikonov, Igor N Swanson, Willie J Roberts, Frank A |
author_facet | Daubert, Diane M Kelley, Joanna L Udod, Yuriy G Habor, Carolina Kleist, Chris G Furman, Ilona K Tikonov, Igor N Swanson, Willie J Roberts, Frank A |
author_sort | Daubert, Diane M |
collection | PubMed |
description | The tooth enamel development gene, enamelin (ENAM), showed evidence of positive selection during a genome-wide scan of human and primate DNA for signs of adaptive evolution. The current study examined the hypothesis that a single-nucleotide polymorphism (SNP) C14625T (rs7671281) in the ENAM gene identified in the genome-wide scan is associated with a change in enamel phenotype. African Americans were selected as the target population, as they have been reported to have a target SNP frequency of approximately 50%, whereas non-Africans are predicted to have a 96% SNP frequency. Digital radiographs and DNA samples from 244 teeth in 133 subjects were analysed, and enamel thickness was assessed in relation to SNP status, controlling for age, sex, tooth number and crown length. Crown length was found to increase with molar number, and females were found to have thicker enamel. Teeth with larger crowns also had thicker enamel, and older subjects had thinner enamel. Linear regression and generalized estimating equations were used to investigate the relationship between enamel thickness of the mandibular molars and ENAM SNP status; enamel in subjects with the derived allele was significantly thinner (P=0.040) when the results were controlled for sex, age, tooth number and crown length. The derived allele demonstrated a recessive effect on the phenotype. The data indicate that thinner dental enamel is associated with the derived ENAM genotype. This is the first direct evidence of a dental gene implicated in human adaptive evolution as having a phenotypic effect on an oral structure. |
format | Online Article Text |
id | pubmed-4932773 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-49327732016-07-14 Human enamel thickness and ENAM polymorphism Daubert, Diane M Kelley, Joanna L Udod, Yuriy G Habor, Carolina Kleist, Chris G Furman, Ilona K Tikonov, Igor N Swanson, Willie J Roberts, Frank A Int J Oral Sci Original Article The tooth enamel development gene, enamelin (ENAM), showed evidence of positive selection during a genome-wide scan of human and primate DNA for signs of adaptive evolution. The current study examined the hypothesis that a single-nucleotide polymorphism (SNP) C14625T (rs7671281) in the ENAM gene identified in the genome-wide scan is associated with a change in enamel phenotype. African Americans were selected as the target population, as they have been reported to have a target SNP frequency of approximately 50%, whereas non-Africans are predicted to have a 96% SNP frequency. Digital radiographs and DNA samples from 244 teeth in 133 subjects were analysed, and enamel thickness was assessed in relation to SNP status, controlling for age, sex, tooth number and crown length. Crown length was found to increase with molar number, and females were found to have thicker enamel. Teeth with larger crowns also had thicker enamel, and older subjects had thinner enamel. Linear regression and generalized estimating equations were used to investigate the relationship between enamel thickness of the mandibular molars and ENAM SNP status; enamel in subjects with the derived allele was significantly thinner (P=0.040) when the results were controlled for sex, age, tooth number and crown length. The derived allele demonstrated a recessive effect on the phenotype. The data indicate that thinner dental enamel is associated with the derived ENAM genotype. This is the first direct evidence of a dental gene implicated in human adaptive evolution as having a phenotypic effect on an oral structure. Nature Publishing Group 2016-06 2016-04-01 /pmc/articles/PMC4932773/ /pubmed/27357321 http://dx.doi.org/10.1038/ijos.2016.1 Text en Copyright © 2016 Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Original Article Daubert, Diane M Kelley, Joanna L Udod, Yuriy G Habor, Carolina Kleist, Chris G Furman, Ilona K Tikonov, Igor N Swanson, Willie J Roberts, Frank A Human enamel thickness and ENAM polymorphism |
title | Human enamel thickness and ENAM polymorphism |
title_full | Human enamel thickness and ENAM polymorphism |
title_fullStr | Human enamel thickness and ENAM polymorphism |
title_full_unstemmed | Human enamel thickness and ENAM polymorphism |
title_short | Human enamel thickness and ENAM polymorphism |
title_sort | human enamel thickness and enam polymorphism |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4932773/ https://www.ncbi.nlm.nih.gov/pubmed/27357321 http://dx.doi.org/10.1038/ijos.2016.1 |
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