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Mup-knockout mice generated through CRISPR/Cas9-mediated deletion for use in urinary protein analysis

机译:通过CRISPR / Cas9介导的缺失产生的Mup基因敲除小鼠用于尿蛋白分析

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摘要

Major urinary proteins (MUPs) are the most abundant protein species in mouse urine, accounting for more than 90% of total protein content. Twenty-one Mup genes and 21 pseudogenes are clustered in a region of around 2 megabase pairs (Mbp) on chromosome 4. A Mup-knockout mouse model would greatly facilitate researches in the field of proteomic analysis of mouse urine. Here, we report the successful knockout of the Mup gene cluster of 2.2 Mbp using the CRISPR/Cas9 system. Homozygous Mup-knockout mice survived to adulthood and exhibited no obvious defects. The patterns of the proteomes of non-MUP urinary proteins in homozygous Mup-knockout mice were similar to those of wild-type mice judged by sodium dodecyl sulfate polyacrylamide gel electrophoresis. The sensitivity of enzyme-linked immunosorbent assay to detect non-MUP urinary protein was significantly enhanced in Mup-knockout mice. In short, we have developed a Mup-knockout mouse model. This mouse model will be useful for the research of urinary biomarker testing that may have relevance for humans.
机译:主要尿蛋白(MUPs)是小鼠尿液中最丰富的蛋白种类,占总蛋白含量的90%以上。 21个Mup基因和21个假基因聚集在4号染色体上大约2兆碱基对(Mbp)的区域中。Mup基因敲除小鼠模型将极大地促进小鼠尿液蛋白质组学分析领域的研究。在这里,我们报告使用CRISPR / Cas9系统成功敲除2.2 Mbp的Mup基因簇。纯合Mup基因敲除小鼠存活到成年,没有明显的缺陷。通过纯十二烷基硫酸钠聚丙烯酰胺凝胶电泳判断,纯合的Mup敲除小鼠中非MUP尿蛋白的蛋白质组模式与野生型小鼠相似。用酶联免疫吸附法检测非MUP尿蛋白的敏感性在Mup基因敲除小鼠中显着增强。简而言之,我们开发了Mup-knockout鼠标模型。该小鼠模型对于研究可能与人类有关的尿液生物标志物测试将是有用的。

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