Unknown

Dataset Information

0

Polymorphisms and variants in the prion protein sequence of European moose (Alces alces), reindeer (Rangifer tarandus), roe deer (Capreolus capreolus) and fallow deer (Dama dama) in Scandinavia.


ABSTRACT: The prion protein (PrP) sequence of European moose, reindeer, roe deer and fallow deer in Scandinavia has high homology to the PrP sequence of North American cervids. Variants in the European moose PrP sequence were found at amino acid position 109 as K or Q. The 109Q variant is unique in the PrP sequence of vertebrates. During the 1980s a wasting syndrome in Swedish moose, Moose Wasting Syndrome (MWS), was described. SNP analysis demonstrated a difference in the observed genotype proportions of the heterozygous Q/K and homozygous Q/Q variants in the MWS animals compared with the healthy animals. In MWS moose the allele frequencies for 109K and 109Q were 0.73 and 0.27, respectively, and for healthy animals 0.69 and 0.31. Both alleles were seen as heterozygotes and homozygotes. In reindeer, PrP sequence variation was demonstrated at codon 176 as D or N and codon 225 as S or Y. The PrP sequences in roe deer and fallow deer were identical with published GenBank sequences.

SUBMITTER: Wik L 

PROVIDER: S-EPMC3399539 | biostudies-literature | 2012 Jul

REPOSITORIES: biostudies-literature

altmetric image

Publications

Polymorphisms and variants in the prion protein sequence of European moose (Alces alces), reindeer (Rangifer tarandus), roe deer (Capreolus capreolus) and fallow deer (Dama dama) in Scandinavia.

Wik Lotta L   Mikko Sofia S   Klingeborn Mikael M   Stéen Margareta M   Simonsson Magnus M   Linné Tommy T  

Prion 20120701 3


The prion protein (PrP) sequence of European moose, reindeer, roe deer and fallow deer in Scandinavia has high homology to the PrP sequence of North American cervids. Variants in the European moose PrP sequence were found at amino acid position 109 as K or Q. The 109Q variant is unique in the PrP sequence of vertebrates. During the 1980s a wasting syndrome in Swedish moose, Moose Wasting Syndrome (MWS), was described. SNP analysis demonstrated a difference in the observed genotype proportions of  ...[more]

Similar Datasets

| S-EPMC7912786 | biostudies-literature
| S-EPMC7699845 | biostudies-literature
| S-EPMC6318929 | biostudies-literature
| S-EPMC4620691 | biostudies-literature
| S-EPMC5726476 | biostudies-literature
| S-EPMC3377593 | biostudies-literature
| S-EPMC1242257 | biostudies-literature
| S-EPMC8101042 | biostudies-literature
| S-EPMC7431400 | biostudies-literature
| S-EPMC7374648 | biostudies-literature