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1.
Tissue Antigens ; 75(3): 218-26, 2010 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-20047645

RESUMEN

Strong linkage disequilibrium (LD) is a characteristic of the major histocompatibility complex (MHC) region, as well as the genome in general in dogs as a consequence of demographic changes with domestication. Disease association studies of MHC haplotypes may be affected by high LD and the resultant shared genetic backgrounds of haplotypes giving associations with linked but non-causative mutations, and also by convergent haplotypes, in which combinations of alleles have arisen independently. This study provides preliminary tools for dog leukocyte antigen (DLA) class II haplotype analysis with 102 single nucleotide polymorphisms (SNPs) identified in 14.6 kb and genotyping of 20 of these SNPs to tag haplotypes in 60 dogs with diabetes mellitus and in 49 non-diabetic dogs. The pattern of LD and analysis of SNP patterns indicated combinations of exon 2 alleles have arisen through both recombination and convergence. For exon 2 haplotypes associated with susceptibility or protection from diabetes mellitus, a region of fixed differences in SNPs across the DQ region was observed, suggesting a region outside exon 2 may be implicated in disease association. Four new DQB1 promoter alleles restricted to diabetic dogs were identified, as well as a substitution difference in the X1 box of the DQB1 promoter that will potentially modify the effect of the protective haplotypes within diabetic dogs.


Asunto(s)
Evolución Biológica , Diabetes Mellitus/veterinaria , Haplotipos , Antígenos de Histocompatibilidad Clase II/genética , Polimorfismo de Nucleótido Simple , Alelos , Animales , Diabetes Mellitus/genética , Diabetes Mellitus/inmunología , Perros , Antígenos HLA/genética , Antígenos HLA/inmunología , Antígenos de Histocompatibilidad Clase II/inmunología , Leucocitos/inmunología , Desequilibrio de Ligamiento , Complejo Mayor de Histocompatibilidad
2.
Heredity (Edinb) ; 95(1): 84-90, 2005 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-16077505

RESUMEN

The genome of the European hedgehog, Erinaceus concolor and E. europaeus, shows a strong signal of cycles of restriction to glacial refugia and postglacial expansion. Patterns of expansion, however, differ for mitochondrial DNA (mtDNA) and preliminary analysis of nuclear markers. In this study, we determine phylogeographic patterns in the hedgehog using two loci of the major histocompatibility complex (MHC), isolated for the first time in hedgehogs. These genes show long persistence times and high polymorphism in many species because of the actions of balancing selection. Among 84 individuals screened for variation, only two DQA alleles were identified in each species, but 10 DQB alleles were found in E. concolor and six in E. europaeus. A strong effect of demography on patterns of DQB variability is observed, with only weak evidence of balancing selection. While data from mtDNA clearly subdivide both species into monophyletic subgroups, the MHC data delineate only E. concolor into distinct subgroups, supporting the preliminary findings of other nuclear markers. Together with differences in variability, this suggests that the refugia history and/or expansion patterns of E. concolor and E. europaeus differ.


Asunto(s)
ADN Mitocondrial/genética , Erizos/clasificación , Erizos/genética , Filogenia , Animales , Europa (Continente) , Genoma , Geografía , Complejo Mayor de Histocompatibilidad , Movimiento , Dinámica Poblacional , Selección Genética
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