Epigenetic structure and the role of polymorphism in the shaping of DNA methylation patterns of equine OAS1 locus View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2014-09-07

AUTHORS

T. Ząbek, E. Semik, M. Wnuk, A. Fornal, A. Gurgul, M. Bugno-Poniewierska

ABSTRACT

DNA methylation patterns and their relation with genetic polymorphisms were determined in the equine OAS1 locus. Genetic variants of OAS1 were previously found to be associated with susceptibility to West Nile virus infections in horses. The subject of the study were white blood cells of 13 juvenile and 13 old horses from AA and HC breed and a set of solid tissues from a single adult horse. The aim was to determine the degree of variation of CpG methylation profiles with concern for tissue type, horse breed and age. Results of direct BSPCR and cloned BSPCR sequencing revealed that all of determined CpG islands (CGIs) were hypermethylated in exception to CGI covering OAS1 promoter and exon 1. One of intragenic CGIs displayed variability of methylation patterns across eight tissue types. The variability of particular sub-types of white blood cells between AA and HC horses were considered as the possible cause of interbreed differences of methylation levels. Comparison of sequence variability between converted and unconverted DNAs of both horse breeds showed polymorphisms of CpG sites to be the source of monoallelic methylation in exception to the polymorphic CpGs located in the OAS1 promoter. Two of them are new polymorphic variants in the OAS1 promoter region. Application of methylation data in conjunction with genetic variation detected at the OAS1 locus might be useful to deepen the knowledge about mechanisms underlying immunity to viral infections in the horse. More... »

PAGES

231-238

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s13353-014-0244-7

DOI

http://dx.doi.org/10.1007/s13353-014-0244-7

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1028135593

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/25195205


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