| Literature DB >> 26851484 |
Haixia Yang1, Wei Zhang2, Shan Lu2, Guangqing Lu2, Hongjuan Zhang2, Yinghua Zhuang2, Yue Wang2, Mengqiu Dong2, Yu Zhang2, Xingang Zhou3, Peng Wang3, Lei Yu4, Fengchao Wang5, Liang Chen6.
Abstract
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.Entities:
Keywords: CRISPR/Cas9; genetically engineered mouse model; knockout; major urinary protein; urine
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Year: 2016 PMID: 26851484 PMCID: PMC4888355 DOI: 10.1093/abbs/gmw003
Source DB: PubMed Journal: Acta Biochim Biophys Sin (Shanghai) ISSN: 1672-9145 Impact factor: 3.848