First Report of Polymorphisms and Genetic Characteristics of Prion-like Protein Gene (PRND) in Cats

Prion diseases are fatal neurodegenerative disorders caused by the misfolding of the normal cellular prion protein (PrP<sup>C</sup>) into its infectious isoform (PrP<sup>Sc</sup>). Although prion diseases in humans, sheep, goats, and cattle have been extensively studied, feline spongiform encephalopathy (FSE) remains poorly understood. Genetic factors, particularly polymorphisms in the prion protein gene (<i>PRNP</i>) and <i>prion-like</i> protein gene (<i>PRND</i>), have been linked to prion disease susceptibility in various species. However, no studies have yet investigated the <i>PRND</i> gene in cats with respect to prion diseases. Therefore, we investigated polymorphisms in the feline <i>PRND gene</i> and analyzed their genetic characteristics. We sequenced the coding region of the <i>PRND</i> gene using samples from 210 domestic cats and determined the genotype and allele frequencies of <i>PRND</i> polymorphisms. We identified thirteen novel single nucleotide polymorphisms (SNPs), including six non-synonymous variants and one insertion/deletion (InDel) in the feline <i>PRND</i> gene. Four of the non-synonymous SNPs were predicted to have deleterious effects on the Doppel protein's structure and function. Notably, the SNP c.97A>G (I33V) showed potential structural clashes, and the others formed additional hydrogen bonds. The LD analysis revealed strong genetic associations between the <i>PRND</i> SNPs and the <i>PRNP</i> InDel, suggesting linkage between these loci in cats. This study identifies novel <i>PRND</i> polymorphisms in domestic cats and provides new insights into the genetic factors underlying feline susceptibility to prion diseases. The strong genetic linkage between <i>PRND</i> and <i>PRNP</i> polymorphisms, coupled with predictions of detrimental effects on Doppel protein structure, suggests that <i>PRND</i> gene variants could influence prion disease progression in cats. These findings provide a foundational framework for future studies on the functional implications of <i>PRND</i> polymorphisms in FSE. To the best of our knowledge, this study is the first report on the genetic characteristics of <i>PRND</i> polymorphisms in cats.

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Journal
Animals
Published
2024-11-27
DOI
https://doi.org/10.3390/ani14233438
Citations
1
Primary Topic
Prion Diseases and Protein Misfolding
Type
article
Field-Weighted Citation Impact
0.23

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article

First Report of Polymorphisms and Genetic Characteristics of Prion-like Protein Gene (PRND) in Cats

Min‐Ju Jeong, Byung‐Hoon Jeong, Yong‐Chan Kim
1 citations
Animals
Prion Diseases and Protein Misfolding
0.23
article

First Report of Polymorphisms and Genetic Characteristics of Prion-like Protein Gene (PRND) in Cats

Min‐Ju Jeong, Byung‐Hoon Jeong, Yong‐Chan Kim
article en
1 citations

Abstract

Prion diseases are fatal neurodegenerative disorders caused by the misfolding of the normal cellular prion protein (PrP<sup>C</sup>) into its infectious isoform (PrP<sup>Sc</sup>). Although prion diseases in humans, sheep, goats, and cattle have been extensively studied, feline spongiform encephalopathy (FSE) remains poorly understood. Genetic factors, particularly polymorphisms in the prion protein gene (<i>PRNP</i>) and <i>prion-like</i> protein gene (<i>PRND</i>), have been linked to prion disease susceptibility in various species. However, no studies have yet investigated the <i>PRND</i> gene in cats with respect to prion diseases. Therefore, we investigated polymorphisms in the feline <i>PRND gene</i> and analyzed their genetic characteristics. We sequenced the coding region of the <i>PRND</i> gene using samples from 210 domestic cats and determined the genotype and allele frequencies of <i>PRND</i> polymorphisms. We identified thirteen novel single nucleotide polymorphisms (SNPs), including six non-synonymous variants and one insertion/deletion (InDel) in the feline <i>PRND</i> gene. Four of the non-synonymous SNPs were predicted to have deleterious effects on the Doppel protein's structure and function. Notably, the SNP c.97A>G (I33V) showed potential structural clashes, and the others formed additional hydrogen bonds. The LD analysis revealed strong genetic associations between the <i>PRND</i> SNPs and the <i>PRNP</i> InDel, suggesting linkage between these loci in cats. This study identifies novel <i>PRND</i> polymorphisms in domestic cats and provides new insights into the genetic factors underlying feline susceptibility to prion diseases. The strong genetic linkage between <i>PRND</i> and <i>PRNP</i> polymorphisms, coupled with predictions of detrimental effects on Doppel protein structure, suggests that <i>PRND</i> gene variants could influence prion disease progression in cats. These findings provide a foundational framework for future studies on the functional implications of <i>PRND</i> polymorphisms in FSE. To the best of our knowledge, this study is the first report on the genetic characteristics of <i>PRND</i> polymorphisms in cats.

AnimalsVol. 14(23)
Gyeongguk National University (KR), Jeonbuk National University (KR)
National Research Foundation of Korea
Life in Land
Openalex Percentile: Top 41%
Prion Diseases and Protein Misfolding
0.23
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