Novel myc oncogene RNA from abortive immunoglobulin-gene recombination in mouse plasmacytomas

GLC Shen-Ong, EJ Keath, SP Piccoli, MD Cole - Cell, 1982 - cell.com
GLC Shen-Ong, EJ Keath, SP Piccoli, MD Cole
Cell, 1982cell.com
We have found that the myc oncogene has been modified by abortive recombination with
the (Y heavy-chain immunoglobulin constant-region(C,) gene in five different mouse
plasmacytoma lines. Recombination occurred approximately 0.8-2.0 kb to the 5'side of two
distinct coding regions, defined by sequence homology between the chicken cellular and
plasmacytoma myc genes. The myc and C, genes were always in opposite transcriptional
orientation, with the recombination site within the C, switch region sequences. DNA …
Summary
We have found that the myc oncogene has been modified by abortive recombination with the (Y heavy-chain immunoglobulin constant-region(C,) gene in five different mouse plasmacytoma lines. Recombination occurred approximately 0.8-2.0 kb to the 5’side of two distinct coding regions, defined by sequence homology between the chicken cellular and plasmacytoma myc genes. The myc and C, genes were always in opposite transcriptional orientation, with the recombination site within the C, switch region sequences. DNA recombination was found to correlate with the production of a novel 2.1 kb species of myc RNA that was 0.4 kb shorter than the normal cellular transcript. No elevated levels of myc RNA were evident, suggesting that DNA rearrangements have altered the myc oncogene product. This oncogene activation corresponds to the chromosomal translocations found in nearly all plasmacytomas.
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