Next Article in Journal
DNA Testing Reveals the Putative Identity of JB55, a 19th Century Vampire Buried in Griswold, Connecticut
Next Article in Special Issue
Identification of Two Independent COL5A1 Variants in Dogs with Ehlers–Danlos Syndrome
Previous Article in Journal
Maternal Haplotypes in DHFR Promoter and MTHFR Gene in Tuning Childhood Acute Lymphoblastic Leukemia Onset-Latency: Genetic/Epigenetic Mother/Child Dyad Study (GEMCDS)
Previous Article in Special Issue
AKNA Frameshift Variant in Three Dogs with Recurrent Inflammatory Pulmonary Disease
Open AccessArticle

Novel Locus Associated with Symmetrical Lupoid Onychodystrophy in the Bearded Collie

1
Department of Animal Science, University of California, Davis, CA 95616, USA
2
Brazilian National Council for Scientific and Technological Development (CNPq) fellow, Brasilia, DF 71605, Brazil
3
Department of Medical and Clinical Genetics, and Department of Veterinary Biosciences, University of Helsinki, 00014 Helsinki, Finland; Folkhälsan Research Center, 00290 Helsinki, Finland
*
Author to whom correspondence should be addressed.
Genes 2019, 10(9), 635; https://doi.org/10.3390/genes10090635
Received: 15 July 2019 / Revised: 16 August 2019 / Accepted: 20 August 2019 / Published: 22 August 2019
(This article belongs to the Special Issue Canine Genetics)
Symmetrical lupoid onychodystrophy (SLO) is characterized by inflammation of the nail bed and nail sloughing that causes affected dogs considerable pain. Disease etiology remains unclear, although an autoimmune component is suspected. A genome-wide association study on Bearded Collies revealed regions of association on canine chromosomes (CFA) 12 and 17. The large region of association on CFA12 likely consists of two smaller linked regions, both of which are also linked to the dog leukocyte antigen (DLA) class II genes. Dogs homozygous for the alternate allele at the top CFA12 SNP also carried two DLA class II risk haplotypes for SLO, and this locus explained most of the increased risk for disease seen throughout the CFA12 region of association. A stronger peak was seen on CFA17 when analysis was done solely on dogs that carried DLA class II risk haplotypes for SLO. The majority of SLO dogs carried a homozygous alternate genotype on CFA12 and at least one CFA17 risk haplotype. Our findings offer progress toward uncovering the genetic basis of SLO. While the contribution of the CFA17 region remains unclear, both CFA12 and CFA17 regions are significantly associated with SLO disease expression in the Bearded Collie and contain potential candidate genes for this disease. View Full-Text
Keywords: SLO; onychodystrophy; dogs; autoimmune; DLA; MHC; genomics; GWAS SLO; onychodystrophy; dogs; autoimmune; DLA; MHC; genomics; GWAS
Show Figures

Figure 1

MDPI and ACS Style

Gershony, L.C.; Belanger, J.M.; Hytönen, M.K.; Lohi, H.; Oberbauer, A.M. Novel Locus Associated with Symmetrical Lupoid Onychodystrophy in the Bearded Collie. Genes 2019, 10, 635.

Show more citation formats Show less citations formats
Note that from the first issue of 2016, MDPI journals use article numbers instead of page numbers. See further details here.

Article Access Map by Country/Region

1
Search more from Scilit
 
Search
Back to TopTop