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A simple PCR-based method for the rapid genotyping of inherited fifthcomplement component (C5)-deficient mice

机译:一种基于PCR的简单方法用于遗传第五代的快速基因分型补体成分(C5)缺陷的小鼠

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摘要

The fifth component of complement (C5) is considered to be the center of complement activation and function. However, there are no genetically engineered knockout mice for this gene, and the only commercially available inherited C5-deficient mice, in which a “TA” nucleotide deletion in the coding frame was previously identified, are in theC57BL/10Sn genetic background rather than the commonly used backgrounds C57BL/6 and BALB/c. Therefore, these mice must be backcrossed into the desired genetic background. Here, we developed an ARMS (amplification refractory mutation system) PCR method using a specific primer pair that was able to discriminate between the genotypes when the resulting product was analyzed by agarose gel electrophoresis. These results were supported by quantitative RT-PCR and semi-quantitative PCR and were consistent with the results from sequencing each backcrossed generation. Using ARMS-PCR method, we generated C5-deficient mice in the C57BL/6 background over 9 backcrossed generations and further verified the phenotype using complement-mediated hemolytic assays. In this study, we describe a simple, rapid and reliable PCR-based method for genotyping inherited C5-deficient mice that may be used to backcross C57BL/10Sn mice into other genetic backgrounds.
机译:补体的第五个成分(C5)被认为是补体激活和功能的中心。但是,没有针对该基因的基因工程基因敲除小鼠,并且唯一可商购获得的遗传性C5缺陷小鼠(先前已识别出编码框中的“ TA”核苷酸缺失)位于C57BL / 10Sn遗传背景中,而不是常用背景C57BL / 6和BALB / c。因此,这些小鼠必须回交到所需的遗传背景。在这里,我们开发了一种使用特定引物对的ARMS(扩增难治性突变系统)PCR方法,当通过琼脂糖凝胶电泳分析所得产物时,该引物对能够区分基因型。这些结果得到定量RT-PCR和半定量PCR的支持,并且与每个回交世代的测序结果一致。使用ARMS-PCR方法,我们在9个回交世代中在C57BL / 6背景中生成了C5缺陷小鼠,并使用补体介导的溶血分析进一步验证了表型。在这项研究中,我们描述了一种简单,快速和可靠的基于PCR的方法,用于对遗传性C5缺陷型小鼠进行基因分型,该方法可用于将C57BL / 10Sn小鼠回交到其他遗传背景中。

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