Detection Method for Gene Doping in a Mouse Model Expressing Human Erythropoietin from Adeno-Associated Virus Vector-9.
Takehito SugasawaAtsushi HirokawaNorihiro OtaniYasuharu KankiKieu Dm NguyenTohru TakemasaKoichi WatanabeYoshinori TakeuchiNaoya YahagiYoichiro TakahashiPublished in: Genes (2024)
With the rapid development of gene therapy technology in recent years, its abuse as a method of sports doping in athletics has become a concern. However, there is still room for improvement in gene-doping testing methods, and a robust animal model needs to be developed. Therefore, the purposes of this study were to establish a model of gene doping using recombinant adeno-associated virus vector-9, including the human erythropoietin gene (rAAV9-h EPO ), and to establish a relevant testing method. First, it was attempted to establish the model using rAAV9-h EPO on mice. The results showed a significant increase in erythrocyte volume accompanied by an increase in spleen weight, confirming the validity of the model. Next, we attempted to detect proof of gene doping by targeting DNA and RNA. Direct proof of gene doping was detected using a TaqMan-qPCR assay with certain primers/probes. In addition, some indirect proof was identified in RNAs through the combination of a TB Green qPCR assay with RNA sequencing. Taken together, these results could provide the foundation for an effective test for gene doping in human athletes in the future.
Keyphrases
- copy number
- genome wide
- gene therapy
- endothelial cells
- genome wide identification
- mouse model
- transition metal
- small molecule
- dna methylation
- body mass index
- gene expression
- adipose tissue
- type diabetes
- high throughput
- single molecule
- mycobacterium tuberculosis
- current status
- transcription factor
- high fat diet induced
- fluorescence imaging
- living cells
- label free
- fluorescent probe