| Literature DB >> 24935699 |
Quan Shen1, Ping Guo1, Baofeng Chai2.
Abstract
A large number of inherited diseases are caused by premature termination codon (PTC) mutations that lead to the degradation of mRNA template. In this report, we developed a dual fluorescent reporter that relied the feature of fluorescent protein coding region to express a fusion protein from pDsRed-EGFPmtag-. Expression of the fusion protein from a single reporter provides a sensitive approach for high-throughput screening of cell-specific PTC events in mixed cell cultures. Results from the read-through analysis of COS7 cells carrying the nonsense mutation pDsRed-EGFPmtag-Y445X treated by PTC 124 showed EGFP transcript level was increased in the COS7 cells treated by PTC124 in a dose-dependent manner. This novel reporter system was applicable to the majority of different PTC patterns and could be used to quantify efficiency of read-through within a single cell or select cells carrying PTC.Entities:
Keywords: Dual fluorescent reporter; Premature termination codon (PTC); Read-through efficiency
Year: 2014 PMID: 24935699 PMCID: PMC4628933 DOI: 10.1007/s10616-014-9728-x
Source DB: PubMed Journal: Cytotechnology ISSN: 0920-9069 Impact factor: 2.058