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Article

First Report of Single Nucleotide Polymorphisms (SNPs) of the Leporine Shadow of Prion Protein Gene (SPRN) and Absence of Nonsynonymous SNPs in the Open Reading Frame (ORF) in Rabbits

by
Sameeullah Memon
1,2,
Zerui Wang
3,
Wen-Quan Zou
3,
Yong-Chan Kim
4,* and
Byung-Hoon Jeong
1,2,3,*
1
Korea Zoonosis Research Institute, Jeonbuk National University, Iksan 54531, Republic of Korea
2
Department of Bioactive Material Sciences and Institute for Molecular Biology and Genetics, Jeonbuk National University, Jeonju 54896, Republic of Korea
3
Department of Pathology, Case Western Reserve University School of Medicine, Cleveland, OH 44106, USA
4
Department of Biological Sciences, Andong National University, Andong 36729, Republic of Korea
*
Authors to whom correspondence should be addressed.
Animals 2024, 14(12), 1807; https://doi.org/10.3390/ani14121807
Submission received: 1 April 2024 / Revised: 7 June 2024 / Accepted: 10 June 2024 / Published: 17 June 2024
(This article belongs to the Section Animal Genetics and Genomics)
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Abstract

:

Simple Summary

The study focuses on the shadow of prion protein (Sho) encoded by the shadow of prion protein gene (SPRN), which associates with PrP and promotes the progression of prion diseases. While genetic polymorphisms in SPRN are linked to susceptibility in several species, rabbit SPRN gene polymorphisms have not been extensively studied. Through amplicon sequencing, we identified novel single nucleotide polymorphisms (SNPs) in the rabbit SPRN gene and found strong linkage disequilibrium (LD) between them. However, strong LD was not observed between polymorphisms in the prion protein gene (PRNP) and SPRN genes in rabbits. Comparison of amino acid sequences revealed differences in SPRN between rabbits and other species susceptible or resistant to prion diseases. This study represents the first examination of genetic features of the rabbit SPRN gene.

Abstract

Prion disorders are fatal infectious diseases that are caused by a buildup of pathogenic prion protein (PrPSc) in susceptible mammals. According to new findings, the shadow of prion protein (Sho) encoded by the shadow of prion protein gene (SPRN) is associated with prion protein (PrP), promoting the progression of prion diseases. Although genetic polymorphisms in SPRN are associated with susceptibility to several prion diseases, genetic polymorphisms in the rabbit SPRN gene have not been investigated in depth. We discovered two novel single nucleotide polymorphisms (SNPs) in the leporine SPRN gene on chromosome 18 and found strong linkage disequilibrium (LD) between them. Additionally, strong LD was not found between the polymorphisms of PRNP and SPRN genes in rabbits. Furthermore, nonsynonymous SNPs that alter the amino acid sequences within the open reading frame (ORF) of SPRN have been observed in prion disease-susceptible animals, but this is the first report in rabbits. As far as we are aware, this study represents the first examination of the genetic features of the rabbit SPRN gene.

1. Introduction

The prion protein (PrP) provides a vital contribution to the emergence of prion diseases, such as Creutzfeldt–Jakob disease (CJD), chronic wasting disease (CWD), scrapie, and bovine spongiform encephalopathy (BSE) [1]. The central nervous system in these disorders is characterized by the buildup of abnormal and misfolded prion proteins (PrPSc), which causes neuron dysfunction and eventual death [2]. The prion protein gene (PRNP) is linked to the development of prion disorders through several genetic attributes. Recent studies have demonstrated that a number of cofactors associated with PrP promote the transformation of normal prion protein (PrPC) to PrPSc [3,4,5]. The shadow of prion protein (Sho), which is translated by the shadow of the prion protein gene (SPRN), is one of these cofactors and plays an important role in the progression of prion diseases [6]. The Sho is classified as a prion family protein and exhibits similarities to PrP because of a glycosylphosphatidylinositol (GPI) anchor and the presence of repeat domains [7]. As the Sho protein is a crucial collaborator in interactions with PrP, genetic variations in the SPRN gene that influence structural alterations of the Sho protein, and its expression physiology have been associated with susceptibility to prion disease.
The rabbit is one of the few species of mammals that appears to be immune to transmissible spongiform encephalopathy (TSE) agents [8]. To date, rabbits inoculated with scrapie, kuru, or CJD agents from mice or sheep have not shown symptoms of TSE diseases [9]. In scrapie-infected mouse neuroblastoma cells, which accumulate mouse PrPSc, neither rabbit PrPC nor chimeric rabbit-mouse PrPC constructs have been transformed into the proteinase-K resistant form [1]. These results imply that the structural features of the leporine PrP are responsible for the resistance to conformational conversion to PrPSc and provide protection against TSE infection. The three-dimensional structure of leporine PrP can help us understand the unique characteristics that set it apart from PrPs of different species [8]. Sequence alignment also reveals 22 different amino acid residues between rabbit and mouse PrPs. The substitution of leporine-specific amino acids (N99G, L108M, N173S, or V214I) in mouse PrP inhibits abnormal conformational changes [10].
The SPRN gene was first identified in the 1990s when scientists began to speculate whether prion-induced disorders might be caused by an unidentified gene [7]. These scientists discovered a novel gene called “shadoo” or SPRN, which encodes a protein resembling the N-terminal region of the PrP. The amino acid sequences of Sho and PrP share a highly similar region with a hydrophobic alanine-rich sequence [5]. This PrP sequence plays a crucial role in interactions between PrPC and PrPSc [11]. In the mammalian brain, the expression profiles of SPRN and PRNP overlapped, and a previous study indicated that the activity of the two genes was co-regulated [5]. Furthermore, in the brains of mice injected with a mice-adapted scrapie strain, there was a significant reduction in the endogenous expression of the Sho protein, suggesting a potential role of Sho in TSE development [12]. Patients with variant CJD carry a null allele associated with the SPRN gene [3]. Additionally, susceptibility to goat scrapie is linked to an insertion variant in the 3′ untranslated region (UTR) of the SPRN gene [4]. Similarly, L-type atypical BSE-affected cattle showed an infrequent sequence variation within the coding sequence of the bovine SPRN gene [5,6] These studies demonstrate a strong relationship between genetic polymorphisms of the SPRN genes and the pathological mechanisms of prion diseases. To date, polymorphisms of the SPRN gene have been examined in prion disease-sensitive and -resistant species [1,6,13,14,15,16,17]. However, the genetic polymorphisms of the leporine SPRN gene have not been explored in depth.
In the current investigation, we used amplicon sequencing and genotyping with SPRN gene-specific primers to examine genetic polymorphisms of the SPRN gene in 207 rabbits and examined the variation characteristics of the rabbit SPRN gene. We also assessed polymorphisms in the SPRN gene for linkage disequilibrium (LD) and investigated LD between SPRN and PRNP single nucleotide polymorphisms (SNPs). Additionally, we identified specific amino acids unique to rabbits by performing multiple sequence alignments with amino acid sequences of Sho protein in the eight prion-related species. Furthermore, we examined the frequencies of genetic polymorphisms within the open reading frame (ORF) region of the SPRN gene between rabbits and species susceptible to prion disease (humans, cattle, goats, and sheep) and those resistant to prion disease (horses and dogs).

2. Materials and Methods

2.1. Ethics Statements

The Institutional Animal Care and Use Committee at Jeonbuk National University (CBNU 2019-058) granted approval for all experimental methods. The Korean Experimental Animal Protection Act was followed for all experiments involving rabbits.

2.2. Genomic DNA Extraction

Blood samples were collected from 207 crossbred rabbits (New Zealand White and Flemish Giant rabbits) in the Nonghyup slaughterhouse in the Republic of Korea. The sample size of the study was sufficient to detect uncommon polymorphisms, including those with genotype frequencies below 1% [18]. Before analysis, ethylenediaminetetraacetic acid (EDTA)-treated whole blood was stored at −80 °C. Genomic DNA was extracted from 200 μL of whole blood using a QIAamp DNA Blood Mini Kit (Qiagen, Valencia, CA, USA) according to the manufacturer’s guidelines.

2.3. Polymerase Chain Reaction (PCR) and DNA Sequencing

PCR was carried out using AxenTM Taq PCR Master Mix (Macrogen, Seoul, Republic of Korea) and gene-specific primers: rabbit SPRN-Forward (5′-GTAAGGCCCAGTGGTGGGAT-3′) and rabbit SPRN-Reverse (5′-GGACTACCGGGATACGGGAT-3′). Primers were designed using the genomic sequence of the rabbit SPRN gene that was deposited at GenBank (Gene ID: 100340524). The detailed experimental procedures followed manufacturers’ protocols, using an annealing temperature of 62 °C for 30 s. PCR reactions were purified using a QIAquick Gel Extraction Kit (Qiagen, Valencia, CA, USA) before being used for sequencing analysis. An ABI 3730XL sequencer (Applied Biosystems, Foster City, CA, USA) was used to perform amplicon sequencing of the PCR products. Finch TV Version 1.4.0 was used to read the sequencing data to carry out the genotype analysis.

2.4. Statistical Analysis

LD analysis was conducted using the Haploview program (version 4.2, https://www.broadinstitute.org/haploview/haploview) (accessed on 1 February 2024). SAS 9.4 program (SAS Institute Inc., Cary, NC, USA) was used to perform chi-square tests to assess distributional differences in Hardy–Weinberg Equilibrium (HWE), genotype, allele, and haplotype frequencies.

2.5. Multiple Sequence Alignments

The information on the Sho protein was acquired from GenBank. This included sequences from humans (Homo sapiens, NP_001012526.2), cattle (Bos taurus, AAY83885.1), sheep (Ovis aries, NP_001156033.1), goats (Capra hircus, AGU17009.1), red deer (Cervus elaphus, ACF24724.1), dogs (Canis lupus familiaris, XP_038296952.1), horses (Equus caballus, XP_023492126.1), and rabbits (Oryctolagus cuniculus, XP_008268877.2). The amino acid sequences of the Sho protein were aligned using the Geneious Bioinformatics program for Sequence Data Analysis (https://www.geneious.com) (accessed on 1 February 2024) based on a progressive alignment method.

2.6. Literature Search

A PubMed literature query was conducted to find reports on SPRN polymorphisms in humans, cattle, goats, sheep, horses, and dogs. Query parameters were “prion”, “SNP”, and “polymorphisms” along with “human”, “cattle”, “goat”, “sheep”, “horse”, or “dog”. After initial assessment of the title and abstract, irrelevant investigations were eliminated. The following criteria for participation were assessed by the authors of this manuscript. First, investigations on genetic polymorphisms of SPRN were listed, followed by full-text articles. The exclusion standards were (1) case reports and (2) reports with insufficient genotype information.

3. Results

3.1. Investigation of Polymorphisms in the SPRN Gene of 207 Rabbits

There are two exons in the rabbit SPRN gene. The ORF region of the leporine SPRN gene was amplified using PCR to investigate genetic polymorphisms. The amplified regions of the SPRN gene comprised 1099 bp, including its ORF as well as a small portion of its 3′ UTR. In exon 2 of the ORF region, we discovered two synonymous SNPs, c.129G>T and c.249A>C (Figure 1). The genotype and allele frequencies of these SNPs in the leporine SPRN gene are shown in Table 1. The genotype frequencies for the polymorphisms were within HWE. We further examined LD values between the two leporine SPRN polymorphisms with |D’| and r2 values (Table 2). Notably, strong LD was observed between the leporine SPRN polymorphisms, c.129G>T and c.249A>C (|D’|=0.67 and r2=1.0). Additionally, we carried out a haplotype analysis for the two polymorphisms of the leporine SPRN gene (Table 3). In the leporine SPRN gene, the GA haplotype was the most prevalent (0.956), followed by TA (0.05) and TC (0.039) (Table 3). Furthermore, we used |D’| and r2 values to examine the LD between PRNP and SPRN SNPs. Data from a previous study [19] were used to present detailed PRNP SNP information. These PRNP and SPRN SNPs were collected from 207 blood samples of different rabbits for LD analysis, and precise LD values are provided (Table 4). Specifically, SPRN SNPs demonstrated exceedingly weak LD with the PRNP c.234C>T SNP.

3.2. Sequence Alignment of the Sho Protein from Multiple Species

The Sho protein sequence of rabbits was compared with that of TSE-susceptible animals, including humans, cattle, sheep, goats, and red deer, and that of TSE-resistant animals, including dogs and horses. A total of 11 amino acids were unique to rabbits: isoleucine (I) at codon 39, threonine (T) at codon 46, proline (P) at codon 64, proline (P) at codon 88, leucine (L) at codon 107, serine (S) at codon 109, threonine (T) at codon 123, cysteine (C) at codon 130, serine (S) at codon 131, tyrosine (Y) at codon 137, and proline (P) at codon 150 (Figure 2).

3.3. Comparing Genetic Polymorphisms of the SPRN Gene among Species

The variations in genetic polymorphisms within the ORF of the SPRN gene in rabbits were compared with those of prion disease-susceptible animals (humans, cattle, goats, and sheep) and those of prion disease-resistant animals (horses and dogs). Remarkably, animals susceptible to prion diseases showed more than seven genetic variations in the SPRN gene. In contrast, prion disease-resistant animals had only one genetic polymorphism in the ORF region of SPRN. Interestingly, our study revealed a unique finding in rabbits: two synonymous SNPs that did not alter the amino acids (Figure 3).

4. Discussion

Sho proteins belong to the PrP family and are primarily expressed in the brain, where they have been shown to accelerate the development of prion disorders [20,24]. According to reports, they affect the developmental processes of mammary glands and embryos [25,26]. The genetic features of the SPRN gene require further study. In the present study, we examined the genetic features of the SPRN gene in rabbits because changes in the genetic makeup of the SPRN gene could influence susceptibility to prion disease through structural modifications and protein expression [3,5,21].
In this study, we discovered two novel synonymous SNPs, c.129G>T and c.249A>C, within the ORF of the rabbit SPRN gene. Notably, no nonsynonymous SNPs have been found in the ORF of this gene. A recent study has shown that synonymous SNPs can affect mRNA integrity, splicing, and gene transcription [15,27]. Therefore, future investigation into the impact of synonymous SNPs in the rabbit SPRN gene on the vulnerability to prion diseases is required. Additionally, the rabbit SPRN gene on chromosome 18 displayed strong genetic LDs between the two SNPs, while the PRNP and SPRN genes in rabbits showed weak LDs. The prion gene family consists of four members, PRNP, PRND, PRNT, and SPRN, with the first three located on chromosome 13 in cattle [28,29,30,31,32]. Previous studies have demonstrated significant genetic LD among these genes [32,33,34,35].
The PRNP SNPs linked to scrapie susceptibility exhibited a strong LD with PRND and PRNT SNPs. This implies a potential link between SNPs in the PRND and PRNT genes and susceptibility to prion diseases [17]. However, SPRN SNPs showed weak LD values with PRNP SNP in this study. Additionally, a previous study found that the dog, a species resistant to prion disease, had low LD values between the PRNP and PRND gene polymorphisms [27]. Since this effect might be generated by an LD block, the causal relationship between the PRNP and SPRN genes was not clear until recently. Subsequently, because the SPRN and PRNP genes are on different chromosomes, prior association investigations for the susceptibility of the SPRN gene to scrapie have not been indicative of an LD block affecting the PRNP gene [17].
Prior reports have shown that several prion-susceptible species, including cattle, sheep, cats, and goats, exhibit a high degree of nonsynonymous polymorphism in SPRN genes, leading to alterations in the amino acid sequence [1,4,5,14,17,22,23,25]. Of note, horses and dogs are prion-resistant species that only have one polymorphism in the SPRN gene [6,15,16]. Overall, synonymous sites have been categorized as neutral in terms of functionality. However, recent conflicting research indicates that synonymous alleles may play important roles in a variety of molecular processes. For example, in human disease correlation studies, synonymous SNPs possess an effect size comparable to nonsynonymous SNPs, according to a recent investigation [3]. We found that rabbits lack two amino acids at positions 115 and 116. In addition, there was a deletion/insertion between positions 39 and 43 in ruminants (Figure 3). This could be interesting in terms of the relationship with the folding process of PrPSc and its connection to susceptibility to prion diseases. Further investigation is highly desirable. In the present study, rabbits were found to have no nonsynonymous SNPs. Although genetic polymorphisms have been examined in a relatively small sample of prion-resistant species compared to prion-susceptible species, the number of prion-resistant species is sufficient to detect rare genetic polymorphisms with afrequency of 1% [6]. The variation in the number of these polymorphisms is evident, which may impact the structure and function of the Sho protein. Consequently, pathogenic changes have a higher probability of developing in a highly polymorphic SPRN gene. Further studies are needed to investigate the significance and function of SPRN genomic features in prion disease susceptibility across a wider range of species.
Although there is much debate about prion susceptibility and resistance, we evaluated species generally reported to have prion diseases and species that showed resistance to prion diseases using several prion infectivity evaluation methods, including protein misfolding cyclic amplification (PMCA), real-time quacking induced conversion (RT-QuIC), and PrP transgenic mice. However, the definitions of “prion susceptible animals” and “prion resistant animals” are often oversimplified to find prion pathomechanism-related unique genetic factors. In the future, it seems desirable to discover factors related to prion diseases by dividing subjects into groups based on their susceptibility or resistance to prion diseases.

5. Conclusions

In conclusion, we identified two synonymous SNPs in the rabbit SPRN gene and determined the genotype, allele, and haplotype frequencies of SPRN gene polymorphisms in rabbits. Additionally, we observed strong genetic LD between rabbit SPRN SNPs located on chromosome 18. Furthermore, our analysis of protein alignment revealed 23 amino acids specific to rabbits. To our knowledge, this is the first investigation of rabbit SPRN gene polymorphisms. Since prion disease-susceptible animals have been found to possess multiple non-synonymous SNPs in the SPRN gene, it is apparent that rabbits lack these non-synonymous SNPs.

Author Contributions

S.M., Y.-C.K. and B.-H.J. conceived and designed the experiment. S.M. performed the experiments. S.M., Y.-C.K. and B.-H.J. analyzed the data. S.M., Z.W., W.-Q.Z., Y.-C.K. and B.-H.J. wrote and edited the article. All authors have read and agreed to the published version of the manuscript.

Funding

This research was supported by the Basic Science Research Program through the National Research Foundation (NRF) of Korea funded by the Ministry of Education (2017R1A6A1A03015876, 2021R1A6A3A01086488). This work also was supported by an NRF grant funded by the Korean government (MSIT) (2021R1A2C1013213, 2022R1C1C2004792). This research was supported by a Korea Basic Science Institute (National Research Facilities and Equipment Center) grant funded by the Ministry of Education (grant No. 2021R1A6C101C369).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

The raw data supporting the conclusions of this article will be made available by the authors upon request.

Conflicts of Interest

The authors declare no conflicts of interest.

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Animals 14 01807 g001
Figure 1. Gene map and electropherograms of single nucleotide polymorphisms (SNPs) of the shadow of prion protein gene (SPRN) identified in the rabbit. (A) Gene map and novel polymorphisms identified in the SPRN gene on chromosome 18 in rabbits. The open reading frame (ORF) within exon 2 is indicated with a black block, and the 5′ and 3′ untranslated regions (UTRs) are indicated with white blocks. Two polymorphisms were found in this study. (B) Electropherograms of novel SNPs in the SPRN gene. The four colors represent DNA bases in the sequence using an ABI 3730 automatic sequencer (blue: cytosine; red: thymine; black: guanine; and green: adenine).
Figure 1. Gene map and electropherograms of single nucleotide polymorphisms (SNPs) of the shadow of prion protein gene (SPRN) identified in the rabbit. (A) Gene map and novel polymorphisms identified in the SPRN gene on chromosome 18 in rabbits. The open reading frame (ORF) within exon 2 is indicated with a black block, and the 5′ and 3′ untranslated regions (UTRs) are indicated with white blocks. Two polymorphisms were found in this study. (B) Electropherograms of novel SNPs in the SPRN gene. The four colors represent DNA bases in the sequence using an ABI 3730 automatic sequencer (blue: cytosine; red: thymine; black: guanine; and green: adenine).
Animals 14 01807 g001
Animals 14 01807 g002
Figure 2. Multiple sequence alignments of the amino acid sequences of various species. Comparison of the amino acid sequence of Sho protein in humans (Homo sapiens, NP_001012526.2), cattle (Bos taurus, AAY83885.1), sheep (Ovis aries, NP_001156033.1), goats (Capra hircus, AGU17009.1), red deer (Cervus elaphus, ACF24724.1), dogs (Canis lupus familiaris, XP_038296952.1), horses (Equus caballus, XP_023492126.1, and rabbits (Oryctolagus cuniculus, XP_008268877.2). Uncolored regions represent differences among species, whereas colors show the similarity of different amino acids.
Figure 2. Multiple sequence alignments of the amino acid sequences of various species. Comparison of the amino acid sequence of Sho protein in humans (Homo sapiens, NP_001012526.2), cattle (Bos taurus, AAY83885.1), sheep (Ovis aries, NP_001156033.1), goats (Capra hircus, AGU17009.1), red deer (Cervus elaphus, ACF24724.1), dogs (Canis lupus familiaris, XP_038296952.1), horses (Equus caballus, XP_023492126.1, and rabbits (Oryctolagus cuniculus, XP_008268877.2). Uncolored regions represent differences among species, whereas colors show the similarity of different amino acids.
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Animals 14 01807 g003
Figure 3. Comparison of genetic polymorphisms in the open reading frame (ORF) of the SPRN gene in species susceptible and resistant to prion disease. Polymorphisms of the SPRN gene have been reported in previous studies [3,4,5,6,16,17,20,21,22,23]. The length of the amino acids in the SPRN gene is depicted by the edged horizontal bar.
Figure 3. Comparison of genetic polymorphisms in the open reading frame (ORF) of the SPRN gene in species susceptible and resistant to prion disease. Polymorphisms of the SPRN gene have been reported in previous studies [3,4,5,6,16,17,20,21,22,23]. The length of the amino acids in the SPRN gene is depicted by the edged horizontal bar.
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Table 1. Genotype and allele frequencies of SPRN gene polymorphisms in rabbits.
Table 1. Genotype and allele frequencies of SPRN gene polymorphisms in rabbits.
SNPsGenotypenGenotype
Frequency		AllelenAllele
Frequency		PICChi-HWP-HW
G>TGG1890.913G3960.9570.10580.03330.9835
GT180.087T180.043
A>CAA1920.929A3990.9640.06652.22140.3293
AC150.071C150.036
PIC: polymorphism information content value; Chi-HW: Chi-square value for Hardy-Weinberg equilibrium; P-HW: p value for Hardy-Weinberg equilibrium.
Table 2. Haplotype frequency of SPRN gene polymorphisms in rabbits.
Table 2. Haplotype frequency of SPRN gene polymorphisms in rabbits.
c.129 G>Tc.249 A>CHaplotype Frequency
ht1GA0.956
ht2TC0.039
ht3TA0.005
Table 3. Linkage disequilibrium (LD) scores between two polymorphisms of the SPRN gene in rabbits.
Table 3. Linkage disequilibrium (LD) scores between two polymorphisms of the SPRN gene in rabbits.
|D’|
r2c.129 G>Tc.249 A>C
c.129 G>T-0.67
c.249 A>C1.0-
The figure above the diagonal indicates |D’| value. The figure below the diagonal indicates r2 value.
Table 4. Linkage disequilibrium (LD) scores among single nucleotide polymorphisms (SNPs) of the SPRN and PRNP genes in rabbits.
Table 4. Linkage disequilibrium (LD) scores among single nucleotide polymorphisms (SNPs) of the SPRN and PRNP genes in rabbits.
|D’|
r2PRNP c.234C>TSPRN c.129 G>TSPRN c.249 A>C
PRNP c.234C>T-0.00.001
SPRN c.129 G>T0.235-0.67
SPRN c.249 A>C0.0371.0-
The figures above the diagonal indicate |D’| values. The figures below the diagonal indicate r2 values.
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MDPI and ACS Style

Memon, S.; Wang, Z.; Zou, W.-Q.; Kim, Y.-C.; Jeong, B.-H. First Report of Single Nucleotide Polymorphisms (SNPs) of the Leporine Shadow of Prion Protein Gene (SPRN) and Absence of Nonsynonymous SNPs in the Open Reading Frame (ORF) in Rabbits. Animals 2024, 14, 1807. https://doi.org/10.3390/ani14121807

AMA Style

Memon S, Wang Z, Zou W-Q, Kim Y-C, Jeong B-H. First Report of Single Nucleotide Polymorphisms (SNPs) of the Leporine Shadow of Prion Protein Gene (SPRN) and Absence of Nonsynonymous SNPs in the Open Reading Frame (ORF) in Rabbits. Animals. 2024; 14(12):1807. https://doi.org/10.3390/ani14121807

Chicago/Turabian Style

Memon, Sameeullah, Zerui Wang, Wen-Quan Zou, Yong-Chan Kim, and Byung-Hoon Jeong. 2024. "First Report of Single Nucleotide Polymorphisms (SNPs) of the Leporine Shadow of Prion Protein Gene (SPRN) and Absence of Nonsynonymous SNPs in the Open Reading Frame (ORF) in Rabbits" Animals 14, no. 12: 1807. https://doi.org/10.3390/ani14121807

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