Genetic characterization of Addison’s disease in Bearded Collies
Abstract Background Primary hypoadrenocorticism (or Addison’s disease, AD) is an autoimmune disease that results in destruction of the adrenal cortex and consequent adrenal insufficiency. The disease has been described in purebred and mixed breed dogs, although some breeds, including the Bearded Col...
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doaj-adb0820fa8f641ef8d99e6ec0d0881da2020-11-26T12:51:16ZengBMCBMC Genomics1471-21642020-11-0121111310.1186/s12864-020-07243-0Genetic characterization of Addison’s disease in Bearded ColliesLiza C. Gershony0Janelle M. Belanger1Marjo K. Hytönen2Hannes Lohi3Thomas R. Famula4Anita M. Oberbauer5Department of Animal Science, University of California-DavisDepartment of Animal Science, University of California-DavisDepartment of Medical and Clinical Genetics, and Department of Veterinary Biosciences, University of HelsinkiDepartment of Medical and Clinical Genetics, and Department of Veterinary Biosciences, University of HelsinkiDepartment of Animal Science, University of California-DavisDepartment of Animal Science, University of California-DavisAbstract Background Primary hypoadrenocorticism (or Addison’s disease, AD) is an autoimmune disease that results in destruction of the adrenal cortex and consequent adrenal insufficiency. The disease has been described in purebred and mixed breed dogs, although some breeds, including the Bearded Collie, are at increased risk for AD. Candidate gene approaches have yielded few associations that appear to be breed-specific. A single other genome-wide association study reported no significant regions of association for AD in Standard Poodles. The present study aimed to identify genomic regions of association for canine AD in Bearded Collies. Results Our study consists of the first genome-wide association analysis to identify a genome-wide significant region of association with canine AD (CFA18). Peaks of suggestive association were also noted on chromosomes 11, 16 and 29. Logistic regression analysis supported an additive effect of risk genotypes at these smaller effect loci on the probability of disease associated with carrying a risk genotype on CFA18. Potential candidate genes involved in adrenal steroidogenesis, regulation of immune responses and/or inflammation were identified within the associated regions of chromosomes 11 and 16. The gene-poor regions of chromosomes 18 and 29 may, however, harbor regulatory sequences that can modulate gene expression and contribute to disease susceptibility. Conclusion Our findings support the polygenic and complex nature of canine AD and identified a strongly associated locus on CFA18 that, when combined with three other smaller effect loci, was predictive of disease. The results offer progress in the identification of susceptibility loci for canine AD in the Bearded Collie. Further studies are needed to confirm association with the suggested candidate genes and identify actual causative mutations involved with AD susceptibility in this breed.http://link.springer.com/article/10.1186/s12864-020-07243-0Addison’s diseaseAutoimmuneDogsGWASGenomicsHypoadrenocorticism |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Liza C. Gershony Janelle M. Belanger Marjo K. Hytönen Hannes Lohi Thomas R. Famula Anita M. Oberbauer |
spellingShingle |
Liza C. Gershony Janelle M. Belanger Marjo K. Hytönen Hannes Lohi Thomas R. Famula Anita M. Oberbauer Genetic characterization of Addison’s disease in Bearded Collies BMC Genomics Addison’s disease Autoimmune Dogs GWAS Genomics Hypoadrenocorticism |
author_facet |
Liza C. Gershony Janelle M. Belanger Marjo K. Hytönen Hannes Lohi Thomas R. Famula Anita M. Oberbauer |
author_sort |
Liza C. Gershony |
title |
Genetic characterization of Addison’s disease in Bearded Collies |
title_short |
Genetic characterization of Addison’s disease in Bearded Collies |
title_full |
Genetic characterization of Addison’s disease in Bearded Collies |
title_fullStr |
Genetic characterization of Addison’s disease in Bearded Collies |
title_full_unstemmed |
Genetic characterization of Addison’s disease in Bearded Collies |
title_sort |
genetic characterization of addison’s disease in bearded collies |
publisher |
BMC |
series |
BMC Genomics |
issn |
1471-2164 |
publishDate |
2020-11-01 |
description |
Abstract Background Primary hypoadrenocorticism (or Addison’s disease, AD) is an autoimmune disease that results in destruction of the adrenal cortex and consequent adrenal insufficiency. The disease has been described in purebred and mixed breed dogs, although some breeds, including the Bearded Collie, are at increased risk for AD. Candidate gene approaches have yielded few associations that appear to be breed-specific. A single other genome-wide association study reported no significant regions of association for AD in Standard Poodles. The present study aimed to identify genomic regions of association for canine AD in Bearded Collies. Results Our study consists of the first genome-wide association analysis to identify a genome-wide significant region of association with canine AD (CFA18). Peaks of suggestive association were also noted on chromosomes 11, 16 and 29. Logistic regression analysis supported an additive effect of risk genotypes at these smaller effect loci on the probability of disease associated with carrying a risk genotype on CFA18. Potential candidate genes involved in adrenal steroidogenesis, regulation of immune responses and/or inflammation were identified within the associated regions of chromosomes 11 and 16. The gene-poor regions of chromosomes 18 and 29 may, however, harbor regulatory sequences that can modulate gene expression and contribute to disease susceptibility. Conclusion Our findings support the polygenic and complex nature of canine AD and identified a strongly associated locus on CFA18 that, when combined with three other smaller effect loci, was predictive of disease. The results offer progress in the identification of susceptibility loci for canine AD in the Bearded Collie. Further studies are needed to confirm association with the suggested candidate genes and identify actual causative mutations involved with AD susceptibility in this breed. |
topic |
Addison’s disease Autoimmune Dogs GWAS Genomics Hypoadrenocorticism |
url |
http://link.springer.com/article/10.1186/s12864-020-07243-0 |
work_keys_str_mv |
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