A gene trap vector system for identifying transcriptionally responsive genes

Enzo Medico, Giovanna Gambarotta, Alessandra Gentile, Paolo M. Comoglio, Philippe Soriano

Research output: Contribution to journalArticlepeer-review

52 Scopus citations


We present a method for fast and efficient trapping of genes whose transcription is regulated by exogenous stimuli. We constructed a promoterless retroviral vector transducing a green fluorescent protein1-nitroreductase2 (GFNR) fusion protein downstream from a splice acceptor site. Flow cytometric analysis of the infected population allows identification and sorting of cells in which the trap is integrated downstream from an active promoter. Conversely, the nitroreductase (NTR) moiety allows pharmacological selection against constitutive GFNR expression. Using hepatocyte growth factor (HGF) stimulation of liver cells3 combined with either positive or negative selection, we recovered cell populations carrying traps in induced or suppressed genes, respectively. Several distinct responsive clones were isolated, and regulated expression of the trapped gene was confirmed at the RNA level. Positive and negative selection can be calibrated to recover traps in genes showing different levels of basal expression or transcriptional regulation. The flexibility and efficiency of the GFNR-based trap screening procedure make it suitable for wide surveys of transcriptionally regulated genes.

Original languageEnglish
Pages (from-to)579-582
Number of pages4
JournalNature Biotechnology
Issue number6
StatePublished - 2001
Externally publishedYes


Dive into the research topics of 'A gene trap vector system for identifying transcriptionally responsive genes'. Together they form a unique fingerprint.

Cite this