Stanton L W, Yang J Q, Eckhardt L A, Harris L J, Birshtein B K, Marcu K B
Proc Natl Acad Sci U S A. 1984 Feb;81(3):829-33. doi: 10.1073/pnas.81.3.829.
The structures of the rearranged c-myc gene products derived from a rcp T(12;15) have been investigated in the MPC-11 (IgG2b kappa) plasmacytoma. The rcp T(12;15) in MPC-11 is a reciprocal exchange between the c-myc gene on chromosome 15 and the immunoglobulin gamma 2a switch region (S gamma 2a) on chromosome 12. The c-myc gene is broken within a 5'-nontranslated exon, thereby separating the promoter region of the normal c-myc gene from its protein coding sequences. This reciprocal rearrangement results in the loss of 11 base pairs of c-myc sequence and 300 base pairs of S gamma 2a sequence at the point of recombination. Sequences that represent the promoter region of the normal c-myc gene are present in the 5'-myc reciprocal fragment. A comparison of the nucleotide sequences at the recombination site of a number of c-myc rearrangements reveals a common feature that may have mechanistic importance for these translocation events.
在MPC-11(IgG2b κ)浆细胞瘤中,对源自rcp T(12;15)的重排c-myc基因产物的结构进行了研究。MPC-11中的rcp T(12;15)是15号染色体上的c-myc基因与12号染色体上的免疫球蛋白γ2a开关区域(Sγ2a)之间的相互交换。c-myc基因在一个5'-非翻译外显子内断裂,从而将正常c-myc基因的启动子区域与其蛋白质编码序列分开。这种相互重排在重组点导致c-myc序列丢失11个碱基对和Sγ2a序列丢失300个碱基对。代表正常c-myc基因启动子区域的序列存在于5'-myc相互片段中。对许多c-myc重排的重组位点处的核苷酸序列进行比较,发现了一个共同特征,这可能对这些易位事件具有机制上的重要性。