Jeong Min-Ju, Kim Yong-Chan, Jeong Byung-Hoon
Korea Zoonosis Research Institute, Jeonbuk National University, Iksan, Jeonbuk, Republic of Korea.
Department of Bioactive Material Sciences, Jeonbuk National University, Jeonju, Jeonbuk, Republic of Korea.
Front Vet Sci. 2024 Jun 17;11:1388339. doi: 10.3389/fvets.2024.1388339. eCollection 2024.
Natural cases of prion disease have not been reported in rabbits, and prior attempts to identify a prion conversion agent have been unsuccessful. However, recent applications of prion seed amplifying experimental techniques have sparked renewed interest in the potential susceptibility of rabbits to prion disease infections. Among several factors related to prion disease, polymorphisms within the prion-like protein gene (), a member of the prion protein family, have been reported as significantly associated with disease susceptibility in various species. Therefore, our study aimed to investigate polymorphisms in the gene of rabbits and analyze their genetic characteristics.
Genomic DNA was extracted from 207 rabbit samples to investigate leporine polymorphisms. Subsequently, amplicon sequencing targeting the coding region of the leporine gene was conducted. Additionally, linkage disequilibrium (LD) analysis was employed to assess the connection within and between loci. The impact of non-synonymous single nucleotide polymorphisms (SNPs) on the Doppel protein was evaluated using PolyPhen-2.
We found nine novel SNPs in the leporine gene: c.18A > G, c.76G > C, c.128C > T, c.146C > T, c.315A > G, c.488G > A, c.525G > C, c.544G > A, and c.579A > G. Notably, seven of these SNPs, excluding c.525G > C and c.579A > G, exhibited strong LD values exceeding 0.3. In addition, LD analysis confirmed a robust link between SNP c.234C > T and SNPs at c.525G > C and c.579A > G. Furthermore, according to PolyPhen-2 and SIFT analyses, the four non-synonymous SNPs were predicted to have deleterious effects on the function or structure of the Doppel protein. However, PANTHER and Missense3D did not indicate such effects.
In this paper, we have identified novel SNPs in the rabbit gene and predicted their potential detrimental effects on protein function or structure through four non-synonymous SNPs. Additionally, we observed a genetic linkage between SNPs in the and genes. These findings may provide insights into understanding the characteristics of rabbits as partially resistant species. To the best of our knowledge, this study is the first to genetically characterize SNPs in rabbits.
兔类尚未报道过自然发生的朊病毒病病例,之前鉴定朊病毒转化因子的尝试均未成功。然而,朊病毒种子扩增实验技术的最新应用引发了对兔类对朊病毒病感染潜在易感性的新关注。在与朊病毒病相关的几个因素中,朊病毒样蛋白基因()是朊病毒蛋白家族的成员,该基因内的多态性已被报道与不同物种的疾病易感性显著相关。因此,我们的研究旨在调查兔类基因的多态性并分析其遗传特征。
从207份兔样本中提取基因组DNA以研究兔类多态性。随后,对兔类基因的编码区进行扩增子测序。此外,采用连锁不平衡(LD)分析来评估位点内部和之间的联系。使用PolyPhen-2评估非同义单核苷酸多态性(SNP)对多普蛋白的影响。
我们在兔类基因中发现了9个新的SNP:c.18A>G、c.76G>C、c.128C>T、c.146C>T、c.315A>G、c.488G>A、c.525G>C、c.544G>A和c.579A>G。值得注意的是,除c.525G>C和c.579A>G外,这些SNP中有7个表现出超过0.3的强LD值。此外,LD分析证实SNP c.234C>T与c.525G>C和c.579A>G处的SNP之间存在紧密联系。此外,根据PolyPhen-2和SIFT分析,这4个非同义SNP预计会对多普蛋白的功能或结构产生有害影响。然而,PANTHER和Missense3D并未显示出此类影响。
在本文中,我们在兔类基因中鉴定了新的SNP,并通过4个非同义SNP预测了它们对蛋白质功能或结构的潜在有害影响。此外,我们观察到基因和基因中的SNP之间存在遗传连锁。这些发现可能有助于深入了解兔类作为部分抗性物种的特征。据我们所知,本研究是首次对兔类SNP进行遗传特征分析。