Retroviral transfer and expression of a humanized, red-shifted green fluorescent protein gene into human tumor cells

Over two-thirds of the current gene therapy protocols use retroviral gene transfer systems. We have developed an efficient retroviral-based method that allows rapid identification of gene transfer in living mammalian cells. Cells were generated containing a gene for an improved (humanized, red-shifted) version of the Aequorea victoria green fluorescent protein (hRGFP) from a retroviral vector. The hRGFP gene was used to produce an amphotropic vector producer cell line that demonstrated vibrant green fluorescence after excitation with blue light. A375 melanoma cells transduced with the retroviral vector demonstrated stable green fluorescence. Both PA317 murine fibroblasts and A375 human cell lines containing the vector were easily detected by FACS analysis. These vectors represent a substantial improvement over currently available gene transfer marking systems. Bright, long-term expression of the hRGFP gene in living eukaryotic cells will advance the study of gene transfer, gene expression, and gene product function in vitro and in vivo particularly for human gene therapy applications.

[1]  M. Chalfie,et al.  Green fluorescent protein as a marker for gene expression. , 1994, Science.

[2]  J R McIntosh,et al.  Analysis of MAP 4 function in living cells using green fluorescent protein (GFP) chimeras , 1995, The Journal of cell biology.

[3]  Tullio Pozzan,et al.  Chimeric green fluorescent protein as a tool for visualizing subcellular organelles in living cells , 1995, Current Biology.

[4]  M. J. Cormier,et al.  Primary structure of the Aequorea victoria green-fluorescent protein. , 1992, Gene.

[5]  T. Hughes,et al.  The jellyfish green fluorescent protein: A new tool for studying ion channel expression and function , 1995, Neuron.

[6]  Douglas C. Youvan,et al.  Red-Shifted Excitation Mutants of the Green Fluorescent Protein , 1995, Bio/Technology.

[7]  K. Umesono,et al.  Localization, trafficking, and temperature-dependence of the Aequorea green fluorescent protein in cultured vertebrate cells. , 1995, Proceedings of the National Academy of Sciences of the United States of America.

[8]  A. Miller,et al.  Redesign of retrovirus packaging cell lines to avoid recombination leading to helper virus production , 1986, Molecular and cellular biology.

[9]  M. Ikawa,et al.  Green fluorescent protein as a marker in transgenic mice , 1995, Development, growth & differentiation.

[10]  K. B. Ward,et al.  X-ray diffraction and time-resolved fluorescence analyses of Aequorea green fluorescent protein crystals. , 1988, The Journal of biological chemistry.

[11]  H. Gerdes,et al.  Visualization of protein transport along the secretory pathway using green fluorescent protein , 1995, FEBS letters.

[12]  O. Shimomura,et al.  Structure of the chromophore of Aequorea green fluorescent protein , 1979 .

[13]  K. B. Ward,et al.  Rapid purification of recombinant green fluorescent protein using the hydrophobic properties of an HPLC size-exclusion column. , 1995, Protein expression and purification.

[14]  W. Hauswirth,et al.  A "humanized" green fluorescent protein cDNA adapted for high-level expression in mammalian cells , 1996, Journal of virology.

[15]  F. Tsuji,et al.  Aequorea green fluorescent protein , 1994, FEBS letters.

[16]  Roger Y. Tsien,et al.  Improved green fluorescence , 1995, Nature.

[17]  R Y Tsien,et al.  Wavelength mutations and posttranslational autoxidation of green fluorescent protein. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[18]  W. M. Westler,et al.  Chemical structure of the hexapeptide chromophore of the Aequorea green-fluorescent protein. , 1993, Biochemistry.

[19]  W. Ward,et al.  Reversible denaturation of Aequorea green-fluorescent protein: physical separation and characterization of the renatured protein. , 1982, Biochemistry.

[20]  Franz Goller,et al.  Implications for lateralization of bird song from unilateral gating of bilateral motor patterns , 1995, Nature.

[21]  D. Prasher,et al.  Using GFP to see the light. , 1995, Trends in genetics : TIG.