Literature DB >> 23912835

PCR-based detection of gene transfer vectors: application to gene doping surveillance.

Irene C Perez1, Caroline Le Guiner, Weiyi Ni, Jennifer Lyles, Philippe Moullier, Richard O Snyder.   

Abstract

Athletes who illicitly use drugs to enhance their athletic performance are at risk of being banned from sports competitions. Consequently, some athletes may seek new doping methods that they expect to be capable of circumventing detection. With advances in gene transfer vector design and therapeutic gene transfer, and demonstrations of safety and therapeutic benefit in humans, there is an increased probability of the pursuit of gene doping by athletes. In anticipation of the potential for gene doping, assays have been established to directly detect complementary DNA of genes that are top candidates for use in doping, as well as vector control elements. The development of molecular assays that are capable of exposing gene doping in sports can serve as a deterrent and may also identify athletes who have illicitly used gene transfer for performance enhancement. PCR-based methods to detect foreign DNA with high reliability, sensitivity, and specificity include TaqMan real-time PCR, nested PCR, and internal threshold control PCR.

Entities:  

Mesh:

Substances:

Year:  2013        PMID: 23912835     DOI: 10.1007/s00216-013-7264-8

Source DB:  PubMed          Journal:  Anal Bioanal Chem        ISSN: 1618-2642            Impact factor:   4.142


  6 in total

1.  Fecal detection of enterotoxigenic Bacteroides fragilis.

Authors:  L A Chen; S Van Meerbeke; E Albesiano; A Goodwin; S Wu; H Yu; K Carroll; C Sears
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2015-07-15       Impact factor: 3.267

2.  Establishment of two quantitative nested qPCR assays targeting the human EPO transgene.

Authors:  E W I Neuberger; I Perez; C Le Guiner; D Moser; T Ehlert; M Allais; P Moullier; P Simon; R O Snyder
Journal:  Gene Ther       Date:  2016-01-11       Impact factor: 5.250

Review 3.  High-throughput methods for genome editing: the more the better.

Authors:  Yong Huang; Meiqi Shang; Tingting Liu; Kejian Wang
Journal:  Plant Physiol       Date:  2022-03-28       Impact factor: 8.340

4.  Microfluidic Quantitative PCR Detection of 12 Transgenes from Horse Plasma for Gene Doping Control.

Authors:  Teruaki Tozaki; Aoi Ohnuma; Mio Kikuchi; Taichiro Ishige; Hironaga Kakoi; Kei-Ichi Hirota; Kanichi Kusano; Shun-Ichi Nagata
Journal:  Genes (Basel)       Date:  2020-04-23       Impact factor: 4.096

5.  Droplet Digital PCR Detection of the Erythropoietin Transgene from Horse Plasma and Urine for Gene-Doping Control.

Authors:  Teruaki Tozaki; Aoi Ohnuma; Masaki Takasu; Mio Kikuchi; Hironaga Kakoi; Kei-Ichi Hirota; Kanichi Kusano; Shun-Ichi Nagata
Journal:  Genes (Basel)       Date:  2019-03-21       Impact factor: 4.096

6.  A next-generation sequencing method for gene doping detection that distinguishes low levels of plasmid DNA against a background of genomic DNA.

Authors:  Eddy N de Boer; Petra E van der Wouden; Lennart F Johansson; Cleo C van Diemen; Hidde J Haisma
Journal:  Gene Ther       Date:  2019-07-11       Impact factor: 5.250

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.