Wabl M, Meyer J, Beck-Engeser G, Tenkhoff M, Burrows P D
Nature. 1985;313(6004):687-9. doi: 10.1038/313687a0.
B lymphocytes may switch from producing an immunoglobulin heavy chain of the mu class to that of the gamma, epsilon or alpha class. To maintain the specificity, the new heavy chain must keep the original variable (V) region; this is achieved by deleting DNA sequences so that the V (consisting of joined VH, diversity (DH) and joining (JH) gene segments) and C (constant) gene segments coding for the new heavy chain are brought into close proximity (reviewed in ref. 5; we do not consider here the mu-delta situation). There are, in principle, three types of chromosomal rearrangements that yield a deletion: rearrangement within a chromatid; unequal sister chromatid exchange (as suggested by Obata et al.); and unequal recombination between chromosomal homologues. We have analysed the arrangement of C mu DNA in clones of the pre-B-cell line 18-81 that switches in vitro from mu to gamma 2b. The clones examined produce either mu, gamma 2b or no immunoglobulin chain. We report here that all the gamma 2b clones had lost at least one copy of C mu and no clones contained three copies of C mu. These findings formally exclude both unequal sister chromatid exchange and recombination between homologues as mechanisms for creating a gene encoding the gamma 2b chain.
B淋巴细胞可能会从产生μ类免疫球蛋白重链转变为产生γ、ε或α类免疫球蛋白重链。为保持特异性,新的重链必须保留原来的可变(V)区;这是通过删除DNA序列来实现的,从而使编码新重链的V(由连接的VH、多样性(DH)和连接(JH)基因片段组成)和C(恒定)基因片段紧密相邻(参考文献5中有综述;我们在此不考虑μ-δ情况)。原则上,有三种类型的染色体重排会导致缺失:染色单体内的重排;不等姐妹染色单体交换(如小畑等人所提出的);以及染色体同源物之间的不等重组。我们分析了前B细胞系18-81的克隆中Cμ DNA的排列情况,该细胞系在体外从μ转换为γ2b。所检测的克隆产生μ、γ2b或不产生免疫球蛋白链。我们在此报告,所有γ2b克隆至少丢失了一个Cμ拷贝,且没有克隆含有三个Cμ拷贝。这些发现正式排除了不等姐妹染色单体交换和同源物之间的重组作为产生编码γ2b链基因的机制。