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基于 PCR 的基因分型检测方法用于检测杰克罗素梗犬中与遗传性胃肠道息肉病相关的种系 APC 变异。

PCR-based genotyping assays to detect germline APC variant associated with hereditary gastrointestinal polyposis in Jack Russell terriers.

机构信息

Laboratory of Veterinary Pathology, Joint Department of Veterinary Medicine, Faculty of Applied Biological Sciences, Gifu University, 1-1 Yanagido, Gifu, 501-1193, Japan.

Laboratory of Veterinary Internal Medicine, Joint Department of Veterinary Medicine, Faculty of Applied Biological Sciences, Gifu University, 1-1 Yanagido, Gifu, 501-1193, Japan.

出版信息

BMC Vet Res. 2021 Jan 18;17(1):32. doi: 10.1186/s12917-020-02731-7.

Abstract

BACKGROUND

The prevalence of gastrointestinal (GI) neoplastic polyps in Jack Russell terriers (JRTs) has increased in Japan since the late 2000s. Recently, we demonstrated that JRTs with GI polyps harbor identical germline variant in the APC gene (c.[462_463delinsTT]) in the heterozygous state. Thus, this disease is an autosomal dominant hereditary disorder. Although the affected JRTs have distinct features, such as the development of multiple GI polyps and an early age of disease onset, genetic testing is indispensable for a definitive diagnosis. Here, polymerase chain reaction (PCR)-based assays capable of detecting germline APC variant were designed and validated using synthetic wild-type and mutant DNAs and genomic DNAs from carrier and non-carrier dogs.

RESULT

First, the PCR-restriction fragment length polymorphism (PCR-RFLP) assay was developed by taking advantage of the germline APC variant creating a new restriction site for MseI. In the PCR-RFLP assay, the 156-bp region containing the variant site was amplified by PCR and subsequently digested with MseI, yielding diagnostic 51 and 58 bp fragments from the mutant allele and allowing determination of the APC genotypes. It was possible to determine the genotypes using genomic DNA extracted from the peripheral blood, buccal swab, or formalin-fixed paraffin-embedded tissue. Next, a TaqMan duplex real-time PCR assay was developed, where a 78-bp region flanking the variant was amplified in the presence of wild-type allele- and mutant allele-specific fluorescent probes. Using blood-derived DNA, altogether 40 cycles of PCR amplification determined the APC genotypes of all examined samples by measuring the fluorescence intensities. Importantly, false-positive and false-negative errors were never detected in both assays.

CONCLUSION

In this study, we developed highly reliable genetic tests for hereditary GI polyposis in JRTs, providing accurate assessment of the presence of the causative germline APC variant. The genotyping assays could contribute to the diagnosis and prevention of hereditary GI polyposis in dogs.

摘要

背景

自 2000 年代后期以来,日本杰克罗素梗犬(JRT)的胃肠道(GI)肿瘤性息肉的患病率有所增加。最近,我们证明了具有 GI 息肉的 JRT 以杂合状态携带 APC 基因(c.[462_463delinsTT])中的相同种系变异。因此,这种疾病是一种常染色体显性遗传性疾病。尽管受影响的 JRT 具有明显的特征,例如多发性 GI 息肉的发展和疾病发病年龄较早,但遗传检测对于明确诊断是必不可少的。在这里,设计并验证了基于聚合酶链反应(PCR)的检测种系 APC 变异的检测方法,该方法利用种系 APC 变异创建了一个新的 MseI 限制性位点。在 PCR-RFLP 检测中,通过 PCR 扩增包含变异位点的 156-bp 区域,然后用 MseI 消化,从突变等位基因产生诊断性的 51 和 58-bp 片段,并允许确定 APC 基因型。可以使用从外周血、口腔拭子或福尔马林固定石蜡包埋组织中提取的基因组 DNA 来确定基因型。接下来,开发了 TaqMan 双重实时 PCR 检测,其中在存在野生型等位基因和突变型等位基因特异性荧光探针的情况下扩增侧翼变异的 78-bp 区域。使用血液衍生的 DNA,通过测量荧光强度,总共进行 40 个循环的 PCR 扩增来确定所有检查样本的 APC 基因型。重要的是,在这两种检测方法中从未检测到假阳性和假阴性错误。

结论

在这项研究中,我们为 JRT 的遗传性 GI 息肉开发了高度可靠的遗传检测方法,为种系 APC 变异的存在提供了准确的评估。基因分型检测方法可以为犬遗传性 GI 息肉的诊断和预防做出贡献。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3f8a/7814721/8a64ec311645/12917_2020_2731_Fig1_HTML.jpg

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