Abstract
Chromosomal translocations of the myc oncogene are a consistent feature of all Burkitt’s lymphomas and are also observed in many murine plasmacytomas. These translocations of myc occur into the immunoglobulin loci and they result in a general increase in myc transcription, but this increase in myc is variable [2, 6, 7, 10, 11, 21, 22]. Since myc may be regulated during the cell cycle (see [9]), deregulation may mean expression at the inappropriate time, which in turn may result in only a modest overall increase in transcription of myc in Burkitt’s lymphomas. On the other hand, the true (and unidentifled) precursor cell of Burkitt’s lymphomas may have a very low level of myc transcription and we are as yet unable to assess properly the true increase in transcription as a consequence of translocations.
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Siebenlist, U., Hennighausen, L., Battey, J., Leder, P. (1985). Chromatin Structure of the Human c-myc Oncogene: Definition of Regulatory Regions and Changes in Burkitt’s Lymphomas. In: Neth, R., Gallo, R.C., Greaves, M.F., Janka, G. (eds) Modern Trends in Human Leukemia VI New Results in Clinical and Biological Research Including Pediatric Oncology. Haematology and Blood Transfusion / Hämatologie und Bluttransfusion, vol 29. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-70385-0_53
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DOI: https://doi.org/10.1007/978-3-642-70385-0_53
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