Reth M, Gehrmann P, Petrac E, Wiese P
Nature. 1986;322(6082):840-2. doi: 10.1038/322840a0.
During B-cell development, the VH genes of immunoglobulin heavy (H) chains are assembled from three different germline components: the variable (VH) segment, the diversity (D) segment and the joining (JH) segment. The joining between two segments involves the recognition of conserved nonamer-heptamer sequences bordering each segment, double-stranded cuts at the heptamer-segment border, and the re-ligation of the two segment ends which have frequently been modified by the deletion and addition of nucleotides. The flexibility of the joint increases VHDJH variability. However, it also results in many pre-B cells which do not produce immunoglobulin H chains and have non-functional VHDJH complexes carrying the VH and JH coding sequences in different reading frames. We show here that such 'null cells' are not dead-end products of the B-cell developmental pathway but can perform a novel VH to VHDJH joining using a 5' VH segment to replace the VH sequence of the VHDJ-H complex. This process can result in the generation of a VHDJ+H complex and the subsequent expression of an immunoglobulin heavy chain.
在B细胞发育过程中,免疫球蛋白重链(H链)的VH基因由三种不同的种系成分组装而成:可变区(VH)片段、多样性区(D)片段和连接区(JH)片段。两个片段之间的连接涉及识别每个片段边界处保守的九聚体-七聚体序列,在七聚体-片段边界处进行双链切割,以及两个经常通过核苷酸缺失和添加而修饰的片段末端的重新连接。连接的灵活性增加了VHDJH的变异性。然而,这也导致许多前B细胞不产生免疫球蛋白H链,并具有携带不同阅读框中VH和JH编码序列的无功能VHDJH复合物。我们在此表明,此类“空细胞”并非B细胞发育途径的终末产物,而是可以利用5' VH片段取代VHDJ-H复合物的VH序列,进行一种新的VH到VHDJH连接。这一过程可导致产生VHDJ+H复合物,并随后表达免疫球蛋白重链。