Suppr超能文献

一种用于柯利犬眼异常的新型快速基因分型技术:基于SYBR Green的实时聚合酶链反应方法,适用于弗林德斯技术协会滤纸上的血液和唾液样本。

A novel rapid genotyping technique for Collie eye anomaly: SYBR Green-based real-time polymerase chain reaction method applicable to blood and saliva specimens on Flinders Technology Associates filter paper.

作者信息

Chang Hye-Sook, Mizukami Keijiro, Yabuki Akira, Hossain Mohammad A, Rahman Mohammad M, Uddin Mohammad M, Arai Toshiro, Yamato Osamu

机构信息

Laboratory of Clinical Pathology, Department of Veterinary Clinical Sciences, Faculty of Agriculture, Kagoshima University, Kohrimoto, Kagoshima, Japan.

出版信息

J Vet Diagn Invest. 2010 Sep;22(5):708-15. doi: 10.1177/104063871002200506.

Abstract

Collie eye anomaly (CEA) is a canine inherited ocular disease that shows a wide variety of manifestations and severity of clinical lesions. Recently, a CEA-associated mutation was reported, and a DNA test that uses conventional polymerase chain reaction (PCR) has now become available. The objective of the current study was to develop a novel rapid genotyping technique by using SYBR Green-based real-time PCR for future large-scale surveys as a key part in the strategy to eradicate CEA by selective breeding. First, a SYBR Green-based real-time PCR assay for genotyping of CEA was developed and evaluated by using purified DNA samples from normal, carrier, and affected Border Collies in which genotypes had previously been determined by conventional PCR. This real-time PCR assay demonstrated appropriate amplifications in all genotypes, and the results were consistent with those of conventional PCR. Second, the availability of Flinders Technology Associates filter paper (FTA card) as DNA templates for the real-time PCR assay was evaluated by using blood and saliva specimens to determine suitability for CEA screening. DNA-containing solution prepared from a disc of blood- or saliva-spotted FTA cards was available directly as templates for the real-time PCR assay when the volume of solution was 2.5% of the PCR mixture. In conclusion, SYBR Green-based real-time PCR combined with FTA cards is a rapid genotyping technique for CEA that can markedly shorten the overall time required for genotyping as well as simplify the sample preparation. Therefore, this newly developed technique suits large-scale screening in breeding populations of Collie-related breeds.

摘要

柯利犬眼异常(CEA)是一种犬类遗传性眼病,临床病变表现形式多样,严重程度各异。最近,有报道称发现了一种与CEA相关的突变,现在已经有了一种使用传统聚合酶链反应(PCR)的DNA检测方法。本研究的目的是开发一种基于SYBR Green的新型实时PCR快速基因分型技术,作为通过选择性育种根除CEA策略的关键部分,用于未来的大规模调查。首先,开发了一种基于SYBR Green的用于CEA基因分型的实时PCR检测方法,并使用来自正常、携带突变和患病边境牧羊犬的纯化DNA样本进行评估,这些样本的基因型先前已通过传统PCR确定。这种实时PCR检测方法在所有基因型中均显示出适当的扩增,结果与传统PCR一致。其次,通过使用血液和唾液样本评估了弗林德斯技术协会滤纸(FTA卡)作为实时PCR检测的DNA模板的可用性,以确定其是否适合CEA筛查。当从血斑或唾液斑FTA卡圆盘制备的含DNA溶液体积为PCR混合物的2.5%时,可直接用作实时PCR检测的模板。总之,基于SYBR Green的实时PCR与FTA卡相结合是一种用于CEA的快速基因分型技术,可显著缩短基因分型所需的总时间,并简化样本制备。因此,这种新开发的技术适用于柯利相关品种繁殖群体的大规模筛查。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验