Yang Haixia, Zhang Wei, Lu Shan, Lu Guangqing, Zhang Hongjuan, Zhuang Yinghua, Wang Yue, Dong Mengqiu, Zhang Yu, Zhou Xingang, Wang Peng, Yu Lei, Wang Fengchao, Chen Liang
College of Life Sciences, Beijing Normal University, Beijing 100875, China National Institute of Biological Sciences, Beijing, Beijing 102206, China.
National Institute of Biological Sciences, Beijing, Beijing 102206, China.
Acta Biochim Biophys Sin (Shanghai). 2016 May;48(5):468-73. doi: 10.1093/abbs/gmw003. Epub 2016 Feb 6.
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.
主要尿液蛋白(MUPs)是小鼠尿液中含量最丰富的蛋白质种类,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号染色体上约2兆碱基对(Mbp)的区域。Mup基因敲除小鼠模型将极大地促进小鼠尿液蛋白质组分析领域的研究。在此,我们报告利用CRISPR/Cas9系统成功敲除了2.2 Mbp的Mup基因簇。纯合Mup基因敲除小鼠存活至成年,未表现出明显缺陷。通过十二烷基硫酸钠聚丙烯酰胺凝胶电泳判断,纯合Mup基因敲除小鼠中非MUP尿液蛋白的蛋白质组模式与野生型小鼠相似。在Mup基因敲除小鼠中,酶联免疫吸附测定法检测非MUP尿液蛋白的灵敏度显著提高。简而言之,我们构建了一个Mup基因敲除小鼠模型。该小鼠模型将有助于开展可能与人类相关的尿液生物标志物检测研究。