After adaptation of a mouse plasma cell tumor, MOPC265, to culture, we
have found several unique chromosomal alterations in addition to the
T(12;15) translocation and trisomy 11 frequently observed in plasmacyt
omas. Among these alterations is a specific coamplification of the c-M
yc and Pvt I gene loci from mouse chromosome 15. Further analysis by f
luorescence in situ hybridization demonstrates that the amplicons of c
-Myc and Pvt I exist as extrachromosomal elements as well as within in
tact chromosomes. Most importantly, the presence of both Pvt I and c-M
yc in these extrachromosomal elements indicates ongoing coselection fo
r these loci in the propagation of MOPC265.