Abstract
Plasmacytoid tumours in mice and Burkitt's lymphomas in humans display characteristic chromosomal translocations involving the c-myc proto-oncogene1,2. Models to explain quantitative changes in c-myc expression have been proposed based on the loss of normal promoters 3-9 as a result of translocation. However, alternative explanations10-16, such as somatic mutation14,17,18, are needed to explain altered c-myc expression in the absence of gene breakage. We present here the nucleotide sequence of the normal murine c-myc gene. Comparison of this sequence with that of a translocated c-myc gene from a murine plasmacytoma reveals complete identity of coding sequence. One nucleotide difference was found in the non-coding first exon. This shows that qualitative changes of the c-myc gene product are not required for ontogenesis in murine plasmacytomas. In contrast, mutations are found in coding18 and non-coding14 regions of translocated c-myc genes from Burkitt's lymphomas, suggesting that the mechanisms by which c-myc is activated in plasmacytomas and Burkitt's lymphomas are different.
| Original language | English |
|---|---|
| Pages (from-to) | 423-425 |
| Number of pages | 3 |
| Journal | Nature |
| Volume | 310 |
| Issue number | 5976 |
| DOIs | |
| Publication status | Published - 1984 |
| Externally published | Yes |