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A genome-wide association study reveals a locus for bilateral iridal hypopigmentation in Holstein Friesian cattle

BACKGROUND: Eye pigmentation abnormalities in cattle are often related to albinism, Chediak-Higashi or Tietz like syndrome. However, mutations only affecting pigmentation of coat color and eye have also been described. Herein 18 Holstein Friesian cattle affected by bicolored and hypopigmented irises...

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Autores principales: Hollmann, Anne K., Bleyer, Martina, Tipold, Andrea, Neßler, Jasmin N., Wemheuer, Wilhelm E., Schütz, Ekkehard, Brenig, Bertram
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5372310/
https://www.ncbi.nlm.nih.gov/pubmed/28356055
http://dx.doi.org/10.1186/s12863-017-0496-4
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author Hollmann, Anne K.
Bleyer, Martina
Tipold, Andrea
Neßler, Jasmin N.
Wemheuer, Wilhelm E.
Schütz, Ekkehard
Brenig, Bertram
author_facet Hollmann, Anne K.
Bleyer, Martina
Tipold, Andrea
Neßler, Jasmin N.
Wemheuer, Wilhelm E.
Schütz, Ekkehard
Brenig, Bertram
author_sort Hollmann, Anne K.
collection PubMed
description BACKGROUND: Eye pigmentation abnormalities in cattle are often related to albinism, Chediak-Higashi or Tietz like syndrome. However, mutations only affecting pigmentation of coat color and eye have also been described. Herein 18 Holstein Friesian cattle affected by bicolored and hypopigmented irises have been investigated. RESULTS: Affected animals did not reveal any ophthalmological or neurological abnormalities besides the specific iris color differences. Coat color of affected cattle did not differ from controls. Histological examination revealed a reduction of melanin pigment in the iridal anterior border layer and stroma in cases as cause of iris hypopigmentation. To analyze the genetics of the iris pigmentation differences, a genome-wide association study was performed using Illumina BovineSNP50 BeadChip genotypes of the 18 cases and 172 randomly chosen control animals. A significant association on bovine chromosome 8 (BTA8) was identified at position 60,990,733 with a -log(10)(p) = 9.17. Analysis of genotypic and allelic dependences between cases of iridal hypopigmentation and an additional set of 316 randomly selected Holstein Friesian cattle controls showed that allele A at position 60,990,733 on BTA8 (P = 4.0e–08, odds ratio = 6.3, 95% confidence interval 3.02–13.17) significantly increased the chance of iridal hypopigmentation. CONCLUSIONS: The clinical appearance of the iridal hypopigmentation differed from previously reported cases of pigmentation abnormalities in syndromes like Chediak-Higashi or Tietz and seems to be mainly of cosmetic character. Iridal hypopigmentation is caused by a reduced content of melanin pigment in the anterior border layer and iridal stroma. A single genomic position on BTA8 was detected to be significantly associated with iridal hypopigmentation in examined cattle. To our knowledge this is the first report about this phenotype in Holstein Friesian cattle. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12863-017-0496-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-53723102017-03-31 A genome-wide association study reveals a locus for bilateral iridal hypopigmentation in Holstein Friesian cattle Hollmann, Anne K. Bleyer, Martina Tipold, Andrea Neßler, Jasmin N. Wemheuer, Wilhelm E. Schütz, Ekkehard Brenig, Bertram BMC Genet Research Article BACKGROUND: Eye pigmentation abnormalities in cattle are often related to albinism, Chediak-Higashi or Tietz like syndrome. However, mutations only affecting pigmentation of coat color and eye have also been described. Herein 18 Holstein Friesian cattle affected by bicolored and hypopigmented irises have been investigated. RESULTS: Affected animals did not reveal any ophthalmological or neurological abnormalities besides the specific iris color differences. Coat color of affected cattle did not differ from controls. Histological examination revealed a reduction of melanin pigment in the iridal anterior border layer and stroma in cases as cause of iris hypopigmentation. To analyze the genetics of the iris pigmentation differences, a genome-wide association study was performed using Illumina BovineSNP50 BeadChip genotypes of the 18 cases and 172 randomly chosen control animals. A significant association on bovine chromosome 8 (BTA8) was identified at position 60,990,733 with a -log(10)(p) = 9.17. Analysis of genotypic and allelic dependences between cases of iridal hypopigmentation and an additional set of 316 randomly selected Holstein Friesian cattle controls showed that allele A at position 60,990,733 on BTA8 (P = 4.0e–08, odds ratio = 6.3, 95% confidence interval 3.02–13.17) significantly increased the chance of iridal hypopigmentation. CONCLUSIONS: The clinical appearance of the iridal hypopigmentation differed from previously reported cases of pigmentation abnormalities in syndromes like Chediak-Higashi or Tietz and seems to be mainly of cosmetic character. Iridal hypopigmentation is caused by a reduced content of melanin pigment in the anterior border layer and iridal stroma. A single genomic position on BTA8 was detected to be significantly associated with iridal hypopigmentation in examined cattle. To our knowledge this is the first report about this phenotype in Holstein Friesian cattle. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12863-017-0496-4) contains supplementary material, which is available to authorized users. BioMed Central 2017-03-29 /pmc/articles/PMC5372310/ /pubmed/28356055 http://dx.doi.org/10.1186/s12863-017-0496-4 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Hollmann, Anne K.
Bleyer, Martina
Tipold, Andrea
Neßler, Jasmin N.
Wemheuer, Wilhelm E.
Schütz, Ekkehard
Brenig, Bertram
A genome-wide association study reveals a locus for bilateral iridal hypopigmentation in Holstein Friesian cattle
title A genome-wide association study reveals a locus for bilateral iridal hypopigmentation in Holstein Friesian cattle
title_full A genome-wide association study reveals a locus for bilateral iridal hypopigmentation in Holstein Friesian cattle
title_fullStr A genome-wide association study reveals a locus for bilateral iridal hypopigmentation in Holstein Friesian cattle
title_full_unstemmed A genome-wide association study reveals a locus for bilateral iridal hypopigmentation in Holstein Friesian cattle
title_short A genome-wide association study reveals a locus for bilateral iridal hypopigmentation in Holstein Friesian cattle
title_sort genome-wide association study reveals a locus for bilateral iridal hypopigmentation in holstein friesian cattle
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5372310/
https://www.ncbi.nlm.nih.gov/pubmed/28356055
http://dx.doi.org/10.1186/s12863-017-0496-4
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