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Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek

Non-inflammatory alopecia is a frequent skin problem in dogs, causing damaged coat integrity and compromised appearance of affected individuals. In this study, we examined the Cesky Fousek breed, which displays atypical recurrent flank alopecia (aRFA) at a high frequency. This type of alopecia can b...

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Autores principales: Neradilová, Silvie, Schauer, Alexandria M., Hayward, Jessica J., Brunner, Magdalena A. T., Bohutínská, Magdalena, Jagannathan, Vidhya, Connell, Laurie B., Boyko, Adam R., Welle, Monika M., Černá Bolfíková, Barbora
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9033119/
https://www.ncbi.nlm.nih.gov/pubmed/35456456
http://dx.doi.org/10.3390/genes13040650
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author Neradilová, Silvie
Schauer, Alexandria M.
Hayward, Jessica J.
Brunner, Magdalena A. T.
Bohutínská, Magdalena
Jagannathan, Vidhya
Connell, Laurie B.
Boyko, Adam R.
Welle, Monika M.
Černá Bolfíková, Barbora
author_facet Neradilová, Silvie
Schauer, Alexandria M.
Hayward, Jessica J.
Brunner, Magdalena A. T.
Bohutínská, Magdalena
Jagannathan, Vidhya
Connell, Laurie B.
Boyko, Adam R.
Welle, Monika M.
Černá Bolfíková, Barbora
author_sort Neradilová, Silvie
collection PubMed
description Non-inflammatory alopecia is a frequent skin problem in dogs, causing damaged coat integrity and compromised appearance of affected individuals. In this study, we examined the Cesky Fousek breed, which displays atypical recurrent flank alopecia (aRFA) at a high frequency. This type of alopecia can be quite severe and is characterized by seasonal episodes of well demarcated alopecic areas without hyperpigmentation. The genetic component responsible for aRFA remains unknown. Thus, here we aimed to identify variants involved in aRFA using a combination of histological, genomic, and transcriptomic data. We showed that aRFA is histologically similar to recurrent flank alopecia, characterized by a lack of anagen hair follicles and the presence of severely shortened telogen or kenogen hair follicles. We performed a genome-wide association study (GWAS) using 216 dogs phenotyped for aRFA and identified associations on chromosomes 19, 8, 30, 36, and 21, highlighting 144 candidate genes, which suggests a polygenic basis for aRFA. By comparing the skin cell transcription pattern of six aRFA and five control dogs, we identified 236 strongly differentially expressed genes (DEGs). We showed that the GWAS genes associated with aRFA are often predicted to interact with DEGs, suggesting their joint contribution to the development of the disease. Together, these genes affect four major metabolic pathways connected to aRFA: collagen formation, muscle structure/contraction, lipid metabolism, and the immune system.
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spelling pubmed-90331192022-04-23 Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek Neradilová, Silvie Schauer, Alexandria M. Hayward, Jessica J. Brunner, Magdalena A. T. Bohutínská, Magdalena Jagannathan, Vidhya Connell, Laurie B. Boyko, Adam R. Welle, Monika M. Černá Bolfíková, Barbora Genes (Basel) Article Non-inflammatory alopecia is a frequent skin problem in dogs, causing damaged coat integrity and compromised appearance of affected individuals. In this study, we examined the Cesky Fousek breed, which displays atypical recurrent flank alopecia (aRFA) at a high frequency. This type of alopecia can be quite severe and is characterized by seasonal episodes of well demarcated alopecic areas without hyperpigmentation. The genetic component responsible for aRFA remains unknown. Thus, here we aimed to identify variants involved in aRFA using a combination of histological, genomic, and transcriptomic data. We showed that aRFA is histologically similar to recurrent flank alopecia, characterized by a lack of anagen hair follicles and the presence of severely shortened telogen or kenogen hair follicles. We performed a genome-wide association study (GWAS) using 216 dogs phenotyped for aRFA and identified associations on chromosomes 19, 8, 30, 36, and 21, highlighting 144 candidate genes, which suggests a polygenic basis for aRFA. By comparing the skin cell transcription pattern of six aRFA and five control dogs, we identified 236 strongly differentially expressed genes (DEGs). We showed that the GWAS genes associated with aRFA are often predicted to interact with DEGs, suggesting their joint contribution to the development of the disease. Together, these genes affect four major metabolic pathways connected to aRFA: collagen formation, muscle structure/contraction, lipid metabolism, and the immune system. MDPI 2022-04-07 /pmc/articles/PMC9033119/ /pubmed/35456456 http://dx.doi.org/10.3390/genes13040650 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Neradilová, Silvie
Schauer, Alexandria M.
Hayward, Jessica J.
Brunner, Magdalena A. T.
Bohutínská, Magdalena
Jagannathan, Vidhya
Connell, Laurie B.
Boyko, Adam R.
Welle, Monika M.
Černá Bolfíková, Barbora
Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
title Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
title_full Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
title_fullStr Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
title_full_unstemmed Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
title_short Genomic and Transcriptomic Characterization of Atypical Recurrent Flank Alopecia in the Cesky Fousek
title_sort genomic and transcriptomic characterization of atypical recurrent flank alopecia in the cesky fousek
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9033119/
https://www.ncbi.nlm.nih.gov/pubmed/35456456
http://dx.doi.org/10.3390/genes13040650
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