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Multiple regulatory...
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Tengvall, Katarina
(författare)
Multiple regulatory variants located in cell type-specific enhancers within the PKP2 locus form major risk and protective haplotypes for canine atopic dermatitis in German shepherd dogs
- E-artikel/E-kapitelEngelska2016
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Nummerbeteckningar
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LIBRIS-ID:21991708
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http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-299868uri
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urn:nbn:se:uu:diva-299868urn
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10.1186/s12863-016-0404-3doi
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Published
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Vetenskapsrådet [521-2012-2826]
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Forskningsrådet Formas [221-2009-1689]
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EU, Europeiska forskningsrådet [310203]
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EU, FP7, Sjunde ramprogrammet [GA-201370]
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gratis
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Background: Canine atopic dermatitis (CAD) is a chronic inflammatory skin disease triggered by allergic reactions involving IgE antibodies directed towards environmental allergens. We previously identified a similar to 1.5 Mb locus on canine chromosome 27 associated with CAD in German shepherd dogs (GSDs). Fine-mapping indicated association closest to the PKP2 gene encoding plakophilin 2. Results: Additional genotyping and association analyses in GSDs combined with control dogs from five breeds with low-risk for CAD revealed the top SNP 27: 19,086,778 (p = 1.4 x 10(-7)) and a rare similar to 48 kb risk haplotype overlapping the PKP2 gene and shared only with other high-risk CAD breeds. We selected altogether nine SNPs (four top-associated in GSDs and five within the similar to 48 kb risk haplotype) that spanned similar to 280 kb forming one risk haplotype carried by 35 % of the GSD cases and 10 % of the GSD controls (OR = 5.1, p = 5.9 x 10(-5)), and another haplotype present in 85 % of the GSD cases and 98 % of the GSD controls and conferring a protective effect against CAD in GSDs (OR = 0.14, p = 0.0032). Eight of these SNPs were analyzed for transcriptional regulation using reporter assays where all tested regions exerted regulatory effects on transcription in epithelial and/or immune cell lines, and seven SNPs showed allelic differences. The DNA fragment with the top-associated SNP 27: 19,086,778 displayed the highest activity in keratinocytes with 11-fold induction of transcription by the risk allele versus 8-fold by the control allele (p(difference) = 0.003), and also mapped close (similar to 3 kb) to an ENCODE skin-specific enhancer region. Conclusions: Our experiments indicate that multiple CAD-associated genetic variants located in cell type-specific enhancers are involved in gene regulation in different cells and tissues. No single causative variant alone, but rather multiple variants combined in a risk haplotype likely contribute to an altered expression of the PKP2 gene, and possibly nearby genes, in immune and epithelial cells, and predispose GSDs to CAD.
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Biuppslag (personer, institutioner, konferenser, titlar ...)
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Kozyrev, Sergey
(författare)
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Kierczak, Marcin
(författare)
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Bergvall, Kerstin
(författare)
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Farias, Fabiana H. G.
(författare)
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Ardesjö-Lundgren, Brita
(författare)
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Olsson, Mia
(författare)
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Murén, Eva
(författare)
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Hagman, Ragnvi
(författare)
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Leeb, Tosso
(författare)
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Pielberg, Gerli
(författare)
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Hedhammar, Åke
(författare)
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Andersson, Göran
(författare)
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Lindblad-Toh, Kerstin268427
(författare)
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Uppsala universitetMedicinska och farmaceutiska vetenskapsområdet
(utgivare)
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Del av/supplement till:channel record
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Ingår i:VärdpublikationBMC Genetics171471-2156
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Tengvall, Katari ...
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Kozyrev, Sergey
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Kierczak, Marcin
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Bergvall, Kersti ...
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Farias, Fabiana ...
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Ardesjö-Lundgren ...
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Olsson, Mia
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Murén, Eva
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Hagman, Ragnvi
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Leeb, Tosso
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Pielberg, Gerli
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Hedhammar, Åke
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Andersson, Göran
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Lindblad-Toh, Ke ...
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