Summary
Using a variety of myc-specific antibodies against bacterially expressed viral and human cellular myc genes and against synthetic peptides, we have characterized viral and cellular myc-gene products and obtained the following results:
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(1)
Immunofluorescence analysis of MC29-transformed fibroblasts sequentially treated with detergent, nucleases and salt indicates that part of the p11Ogag-myc remains insoluble suggesting its association with the so-called nuclear matrix.
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(2)
Immune-affinity purified p11Ogag-myc protein inhibits transcription of the Adenovirus 2 major late promoter (Ad2 MLP) two- to fourfold if added to in vitro transcription systems.
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(3)
The c-myc gene product expressed in avian lymphoma (RP9) cells was identified as a protein of 55,000 molecular weight, p55c-myc, similar to the avian viral p55v-myc protein of OK10 cells.
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(4)
Myc-specific antibodies gave rise to nuclear fluorescence in HeLa cells and precipitated two proteins of about 62,000 and 49,000 molecular weights which were competed out by the appropriate antigens.
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(5)
Mitogen-stimulated lymphocytes exhibit two novel proteins of similar size detected by myc-specific antibodies.
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References
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Moelling, K. et al. (1984). Properties of the myc-Gene Product: Nuclear Association, Inhibition of Transcription and Activation in Stimulated Lymphocytes. In: Potter, M., Melchers, F., Weigert, M. (eds) Oncogenes in B-Cell Neoplasia. Current Topics in Microbiology and Immunology, vol 113. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-69860-6_34
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DOI: https://doi.org/10.1007/978-3-642-69860-6_34
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