Walfield A, Selsing E, Arp B, Storb U
Nucleic Acids Res. 1981 Mar 11;9(5):1101-9. doi: 10.1093/nar/9.5.1101.
The myeloma variant NS-1n has lost the functional immunoglobulin kappa gene which is present in its parent, myeloma MOPC-21. The variant retains a nonfunctional rearranged gene, M.21N, which undergoes RNA transcription and processing to yield a mature size kmRNA. This kRNA, however, is not translated into kappa polypeptide chains. The nonfunctional gene was cloned into Charon 4A to determine the basis for its inactivity. Nucleotide sequence analysis of a DNA fragment overlapping the V-J recombination site in the M.21N gene indicated that a misalignment had taken place during somatic recombination. This misalignment results in a deletion of four nucleotides at the 3' end of the V gene and, thus, a translational reading frame shift. In other respects the M.21n V gene, which corresponds to a different VK subgroup than the functional gene of MOPC-21, appears normal.
骨髓瘤变体NS-1n已失去其亲本骨髓瘤MOPC-21中存在的功能性免疫球蛋白κ基因。该变体保留了一个无功能的重排基因M.21N,它经过RNA转录和加工产生成熟大小的κmRNA。然而,这种κRNA不会被翻译成κ多肽链。将该无功能基因克隆到Charon 4A中以确定其无活性的基础。对与M.21N基因中V-J重组位点重叠的DNA片段进行核苷酸序列分析表明,在体细胞重组过程中发生了错配。这种错配导致V基因3'端缺失四个核苷酸,从而导致翻译阅读框移位。在其他方面,与MOPC-21的功能基因属于不同VK亚组的M.21n V基因看起来是正常的。