Variation in the prion protein gene (PRNP) open reading frame sequence in French cervids
Johann Laubier, Anne Van De Wiele, Aurélie Barboiron, Denis Laloë, Christine Saint-Andrieux, Johan Castille, Emma Meloni, Sonja Ernst, Maryline Pellerin, Sandrine Floriot, Nathalie Daniel-Carlier, Bruno Passet, Joël Merlet, Hélène Verheyden, Vincent Béringue, Olivier Andréoletti

TL;DR
This study examines genetic variation in the prion protein gene (PRNP) in French roe deer and red deer to understand their susceptibility to chronic wasting disease.
Contribution
The study provides a detailed analysis of PRNP polymorphisms in French cervids, revealing species-specific genetic diversity patterns.
Findings
French roe deer showed a monomorphic PRNP gene except for one heterozygous animal with a G37A mutation.
Red deer displayed multiple non-synonymous and synonymous substitutions, including a new 24bp deletion.
Significant regional variation in PRNP polymorphism frequencies was observed among French regions.
Abstract
The recent emergence of chronic wasting disease (CWD) in Europe has become a new public health risk for monitoring of wild and farmed cervids. This disease, due to prions, has proliferated in North America in a contagious manner. In several mammalian species, polymorphisms in the prion protein gene (PRNP) play a crucial role in the susceptibility to prions and their spread. To obtain a reliable picture of the distribution of PRNP polymorphisms in the two most common cervid species in France, we sequenced the open reading frame (ORF) of this gene in 2114 animals, 1116 roe deer (Capreolus capreolus) and 998 red deer (Cervus elaphus). Selection criteria such as historical origin, spatial distribution and sex ratio have been integrated to establish this sample collection. Except for one heterozygous animal with a non-synonymous mutation at codon 37 (G37A), all the 1116 French roe deer were…
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Taxonomy
TopicsPrion Diseases and Protein Misfolding · Trace Elements in Health · Metallurgy and Material Science
