Dunnick W, Baumgartner J, Fradkin L, Schultz C, Szurek P
Gene. 1985;39(2-3):287-92. doi: 10.1016/0378-1119(85)90325-7.
The chromosomal translocation associated with many tumors of immunoglobulin-producing cells frequently results in the joining of the immunoglobulin heavy-chain locus and the c-myc oncogene. This translocation of c-myc has profound structural and functional consequences for the oncogene, including loss of the 5' end of the gene and transcriptional deregulation. We report in this communication that translocation results in a new methylation pattern of c-myc. In normal kidney and liver tissue, the c-myc gene is methylated at its 3' end. The translocated gene in plasmacytoma DNA is extensively demethylated. On the other hand, the nonrearranged c-myc gene in plasmacytoma DNA (which is transcriptionally silent) is extensively methylated. In addition, we confirm the nucleotide sequence (with 19 discrepancies out of 1400 bp) 5' to the murine c-myc gene, as reported by Corcoran et al. [Cell 40 (1985) 71-79].
与许多免疫球蛋白产生细胞肿瘤相关的染色体易位常常导致免疫球蛋白重链基因座与c-myc癌基因的连接。c-myc的这种易位对癌基因具有深远的结构和功能影响,包括基因5'端的缺失和转录失调。我们在本通讯中报告,易位导致c-myc出现新的甲基化模式。在正常肾脏和肝脏组织中,c-myc基因在其3'端发生甲基化。浆细胞瘤DNA中的易位基因广泛去甲基化。另一方面,浆细胞瘤DNA中未重排的c-myc基因(转录沉默)则广泛甲基化。此外,正如Corcoran等人[《细胞》40(1985)71 - 79]所报道的,我们确认了小鼠c-myc基因5'端的核苷酸序列(1400 bp中有19处差异)。