Royo L J, Fernández I, Azor P J, Alvarez I, Pérez-Pardal L, Goyache F
Servicio Regional de Investigación y Desarrollo Agroalimentario del Principado de Asturias-Somió, C/Camino de los Claveles 604, E-33203 Gijón (Asturias), Spain.
J Anim Sci. 2008 Jun;86(6):1291-5. doi: 10.2527/jas.2007-0498. Epub 2008 Feb 29.
The aim of this note is to describe a reliable, fast, and cost-effective real-time PCR method for routine genotyping of mutations responsible for most coat color variation in horses. The melanocortin-1 receptor, Agouti-signaling peptide, and membrane-associated transporter protein alleles were simultaneously determined using 2 PCR protocols. The assay described here is an alternative method for routine genotyping of a defined number of polymorphisms. Allelic variants are detected in real time and no post-PCR manipulations are required, therefore limiting costs and possible carryover contamination. Data can be copied to a Microsoft Excel spreadsheet for semiautomatic determination of the genotype using a macro freely available at http://www.igijon.com/personales/fgoyache/software_i.htm (last accessed February 26, 2007). The performance of the method is demonstrated on 156 Spanish Purebred horses.
本笔记的目的是描述一种可靠、快速且经济高效的实时PCR方法,用于对导致马匹大多数毛色变异的突变进行常规基因分型。使用2种PCR方案同时测定黑素皮质素-1受体、刺鼠信号肽和膜相关转运蛋白等位基因。此处描述的检测方法是对特定数量多态性进行常规基因分型的替代方法。等位基因变体可实时检测,无需PCR后操作,因此可降低成本并避免可能的交叉污染。数据可复制到Microsoft Excel电子表格中,使用可从http://www.igijon.com/personales/fgoyache/software_i.htm免费获取的宏(最后访问时间为2007年2月26日)半自动确定基因型。该方法的性能在156匹西班牙纯种马中得到了验证。