Citation
- Authors: Vallejos, M., Ramdohr, P., Valiente-Echeverria, F., Tapia, K., Rodriguez, F. E., Lowy, F., Huidobro-Toro, J. P., Dangerfield, J. A., Lopez-Lastra, M.
- Year: 2010
- Journal: Nucleic Acids Res 38 618-32
- Applications: in vitro / DNA / jetPEI
- Cell types:
- Name: HEK-293T
Description: Human embryonic kidney Fibroblast
Known as: HEK293T, 293T - Name: HeLa
Description: Human cervix epitheloid carcinoma cells - Name: NIH/3T3
Description: Murine embryonic fibroblasts
Known as: NIH/3T3, 3T3
- Name: HEK-293T
Abstract
In this study, we demonstrate the identification of an internal ribosome entry site (IRES) within the 5'-untranslated region (5'-UTR) of the mouse mammary tumor virus (MMTV). The 5'-UTR of the full-length mRNA derived from the infectious, complete MMTV genome was cloned into a dual luciferase reporter construct containing an upstream Renilla luciferase gene (RLuc) and a downstream firefly luciferase gene (FLuc). In rabbit reticulocyte lysate, the MMTV 5'-UTR was capable of driving translation of the second cistron. In vitro translational activity from the MMTV 5'-UTR was resistant to the addition of m(7)GpppG cap-analog and cleavage of eIF4G by foot-and-mouth disease virus (FMDV) L-protease. IRES activity was also demonstrated in the Xenopus laevis oocyte by micro-injection of capped and polyadenylated bicistronic RNAs harboring the MMTV-5'-UTR. Finally, transfection assays showed that the MMTV-IRES exhibits cell type-dependent translational activity, suggesting a requirement for as yet unidentified cellular factors for its optimal function.