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and -
in Mouse Cells
1 Institute of Biochemistry, Biological Research Center, Hungarian Academy of Sciences, Szeged, H-6701
and2 Institute of Microbiology, Medical University of Szeged, H-6720, Hungary
Human interferon-
1 and interferon-
genes with their flanking regions were introduced into mouse LMTK- cells. Although transfected cells contained the interferon genes with a similar copy number and produced a similar amount of interferon-specific mRNA, cells containing the human interferon-
gene secreted about 10 times more human interferon than cells transfected with the human interferon-
1 gene. When the coding region of the interferon-
gene was replaced by that of the interferon-
1 gene (hybrid interferon
/
gene), the human interferon production of transfected cells fell by approx. one order of magnitude. These results show that in the case of exogenous interferon genes a translational or post-translational mechanism might significantly affect the final level of human interferons, resulting in higher titres of interferon-
than of interferon-
.
Keywords: interferon (HuIFN-
, -
), transfection, regulation
Present address: Institut für Genetik, Universität zu Köln, Weyertal 121, 5000 Köln 41, F.R.G.
Received 9 November 1987;
accepted 8 July 1988.
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