Erikson J, Finger L, Sun L, ar-Rushdi A, Nishikura K, Minowada J, Finan J, Emanuel B S, Nowell P C, Croce C M
Science. 1986 May 16;232(4752):884-6. doi: 10.1126/science.3486470.
Two human T-cell leukemias carrying a t(8;14)(q24;q11) chromosome translocation were studied for rearrangements and expression of the c-myc oncogene. For one leukemia, rearrangement was detected in a region immediately distal (3') to the c-myc locus; no rearrangements of c-myc were observed in the second case (DeF). However, studies with hybrids between human and mouse leukemic T cells indicated that in the leukemic cells of DeF, the breakpoint in chromosome 14 occurred between genes for the variable (V alpha) and the constant (C alpha) regions for the alpha chain of the T-cell receptor. The C alpha locus had translocated to a region more than 38 kilobases 3' to the involved c-myc oncogene. Since human c-myc transcripts were expressed only in hybrids carrying the 8q+ chromosome but not in hybrids containing the normal chromosome 8, it is concluded that the translocation of the C alpha locus 3' to the c-myc oncogene can result in its transcriptional deregulation.
对两例携带t(8;14)(q24;q11)染色体易位的人类T细胞白血病进行了c-myc癌基因重排和表达的研究。对于其中一例白血病,在紧邻c-myc基因座远端(3')的区域检测到重排;在第二例(DeF)中未观察到c-myc重排。然而,人与小鼠白血病T细胞杂交研究表明,在DeF白血病细胞中,14号染色体的断点发生在T细胞受体α链可变区(Vα)和恒定区(Cα)基因之间。Cα基因座已易位至受累c-myc癌基因3'端超过38千碱基的区域。由于人类c-myc转录本仅在携带8q+染色体的杂交细胞中表达,而在含有正常8号染色体的杂交细胞中不表达,因此得出结论,Cα基因座向c-myc癌基因3'端的易位可导致其转录失调。