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PTPN22 polymorphisms may indicate a role for this gene in atopic dermatitis in West Highland white terriers
BACKGROUND: Canine atopic dermatitis is an allergic inflammatory skin disease common in West Highland white terriers. A genome-wide association study for atopic dermatitis in a population of West Highland white terriers identified a 1.3 Mb area of association on CFA17 containing canine protein tyros...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3271996/ https://www.ncbi.nlm.nih.gov/pubmed/22208456 http://dx.doi.org/10.1186/1756-0500-4-571 |
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author | Roque, Joana Barros O'Leary, Caroline A Kyaw-Tanner, Myat Duffy, David L Gharahkhani, Puya Vogelnest, Linda Mason, Kenneth Shipstone, Michael |
author_facet | Roque, Joana Barros O'Leary, Caroline A Kyaw-Tanner, Myat Duffy, David L Gharahkhani, Puya Vogelnest, Linda Mason, Kenneth Shipstone, Michael |
author_sort | Roque, Joana Barros |
collection | PubMed |
description | BACKGROUND: Canine atopic dermatitis is an allergic inflammatory skin disease common in West Highland white terriers. A genome-wide association study for atopic dermatitis in a population of West Highland white terriers identified a 1.3 Mb area of association on CFA17 containing canine protein tyrosine phosphatase non-receptor type 22 (lymphoid) PTPN22. This gene is a potential candidate gene for canine atopic dermatitis as it encodes a lymphoid-specific signalling mediator that regulates T-cell and possibly B-cell activity. FINDINGS: Sequencing of PTPN22 in three atopic and three non-atopic West Highland white terriers identified 18 polymorphisms, including five genetic variants with a bioinformatically predicted functional effect. An intronic polymorphic repeat sequence variant was excluded as the cause of the genome-wide association study peak signal, by large-scale genotyping in 72 West Highland white terriers (gene-dropping simulation method, P = 0.01). CONCLUSIONS: This study identified 18 genetic variants in PTPN22 that might be associated with atopic dermatitis in West Highland white terriers. This preliminary data may direct further study on the role of PTPN22 in this disease. Large scale genotyping and complementary genomic and proteomic assays would be required to assess this possibility. |
format | Online Article Text |
id | pubmed-3271996 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-32719962012-02-04 PTPN22 polymorphisms may indicate a role for this gene in atopic dermatitis in West Highland white terriers Roque, Joana Barros O'Leary, Caroline A Kyaw-Tanner, Myat Duffy, David L Gharahkhani, Puya Vogelnest, Linda Mason, Kenneth Shipstone, Michael BMC Res Notes Short Report BACKGROUND: Canine atopic dermatitis is an allergic inflammatory skin disease common in West Highland white terriers. A genome-wide association study for atopic dermatitis in a population of West Highland white terriers identified a 1.3 Mb area of association on CFA17 containing canine protein tyrosine phosphatase non-receptor type 22 (lymphoid) PTPN22. This gene is a potential candidate gene for canine atopic dermatitis as it encodes a lymphoid-specific signalling mediator that regulates T-cell and possibly B-cell activity. FINDINGS: Sequencing of PTPN22 in three atopic and three non-atopic West Highland white terriers identified 18 polymorphisms, including five genetic variants with a bioinformatically predicted functional effect. An intronic polymorphic repeat sequence variant was excluded as the cause of the genome-wide association study peak signal, by large-scale genotyping in 72 West Highland white terriers (gene-dropping simulation method, P = 0.01). CONCLUSIONS: This study identified 18 genetic variants in PTPN22 that might be associated with atopic dermatitis in West Highland white terriers. This preliminary data may direct further study on the role of PTPN22 in this disease. Large scale genotyping and complementary genomic and proteomic assays would be required to assess this possibility. BioMed Central 2011-12-30 /pmc/articles/PMC3271996/ /pubmed/22208456 http://dx.doi.org/10.1186/1756-0500-4-571 Text en Copyright ©2011 Roque et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Short Report Roque, Joana Barros O'Leary, Caroline A Kyaw-Tanner, Myat Duffy, David L Gharahkhani, Puya Vogelnest, Linda Mason, Kenneth Shipstone, Michael PTPN22 polymorphisms may indicate a role for this gene in atopic dermatitis in West Highland white terriers |
title | PTPN22 polymorphisms may indicate a role for this gene in atopic dermatitis in West Highland white terriers |
title_full | PTPN22 polymorphisms may indicate a role for this gene in atopic dermatitis in West Highland white terriers |
title_fullStr | PTPN22 polymorphisms may indicate a role for this gene in atopic dermatitis in West Highland white terriers |
title_full_unstemmed | PTPN22 polymorphisms may indicate a role for this gene in atopic dermatitis in West Highland white terriers |
title_short | PTPN22 polymorphisms may indicate a role for this gene in atopic dermatitis in West Highland white terriers |
title_sort | ptpn22 polymorphisms may indicate a role for this gene in atopic dermatitis in west highland white terriers |
topic | Short Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3271996/ https://www.ncbi.nlm.nih.gov/pubmed/22208456 http://dx.doi.org/10.1186/1756-0500-4-571 |
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