Geographic variation in the PRNP gene and its promoter, and their relationship to chronic wasting disease in North American deer.

IF 1.6 3区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Prion Pub Date : 2020-12-01 DOI:10.1080/19336896.2020.1796250
Robert M Zink, Nadje Najar, Hernán Vázquez-Miranda, Brittaney L Buchanan, Duan Loy, Bruce W Brodersen
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引用次数: 9

Abstract

PRNP genotypes, number of octarepeats (PHGGGWGQ) and indels in the PRNP promoter can influence the progression of prion disease in mammals. We found no relationship between presence of promoter indels in white-tailed deer and mule deer from Nebraska and CWD presence. White-tailed deer with the 95 H allele and G20D mule deer were more likely to be CWD-free, but unlike other studies white-tailed deer with the 96S allele(s) were equally likely to be CWD-free. We provide the first information on PRNP genotypes and indels in the promoter for Key deer (all homozygous 96SS) and Coues deer (lacked 95 H and 96S alleles, but possessed a uniquely high frequency of 103 T). All deer surveyed were homozygous for three tandem octarepeats.

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北美鹿PRNP基因及其启动子的地理变异及其与慢性消耗性疾病的关系
PRNP基因型、八联体数(PHGGGWGQ)和PRNP启动子中的索引可影响哺乳动物朊病毒疾病的进展。我们发现内布拉斯加州白尾鹿和骡鹿的启动子索引的存在与CWD的存在没有关系。携带95 H等位基因的白尾鹿和G20D骡鹿更有可能无cwd,但与其他研究不同的是,携带96S等位基因的白尾鹿同样有可能无cwd。我们首次提供了Key鹿(全部为纯合子96SS)和Coues鹿(缺少95个H和96S等位基因,但具有独特的103 T高频)的PRNP基因型和启动子索引的信息。所有被调查的鹿都是三个连续八重复的纯合子。
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来源期刊
Prion
Prion 生物-生化与分子生物学
CiteScore
5.20
自引率
4.30%
发文量
13
审稿时长
6-12 weeks
期刊介绍: Prion is the first international peer-reviewed open access journal to focus exclusively on protein folding and misfolding, protein assembly disorders, protein-based and structural inheritance. The goal is to foster communication and rapid exchange of information through timely publication of important results using traditional as well as electronic formats. The overriding criteria for publication in Prion are originality, scientific merit and general interest.
期刊最新文献
Chronic Wasting Disease Research in North America: A systematic review highlighting species-wise and interdisciplinary research trends. Specific early electroencephalogram for the diagnosis of sporadic Creutzfeldt-Jakob disease. Chronic wasting disease as a model for human prion therapy. Functional amyloid protein FXR1 is recruited into neuronal stress granules. Prion 2024 conference: from two decades of growth to a new journey forward.
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