Darlow John M, Stott David I
Department of Immunology, Level 4, Glasgow Biomedical Research Centre, 120 University Place, Glasgow, G12 8TA, UK.
Immunogenetics. 2006 Jul;58(7):511-22. doi: 10.1007/s00251-006-0113-6. Epub 2006 May 17.
Over the past 20 years, many DNA sequences have been published suggesting that all or part of the V(H) segment of a rearranged immunoglobulin gene may be replaced in vivo. Two different mechanisms appear to be operating. One of these is very similar to primary V(D)J recombination, involving the RAG proteins acting upon recombination signal sequences, and this has recently been proven to occur. Other sequences, many of which show partial V(H) replacements with no addition of untemplated nucleotides at the V(H)-V(H) joint, have been proposed to occur by an unusual RAG-mediated recombination with the formation of hybrid (coding-to-signal) joints. These appear to occur in cells already undergoing somatic hypermutation in which, some authors are convinced, RAG genes are silenced. We recently proposed that the latter type of V(H) replacement might occur by homologous recombination initiated by the activity of AID (activation-induced cytidine deaminase), which is essential for somatic hypermutation and gene conversion. The latter has been observed in other species, but not in human Ig genes, so far. In this paper, we present a new analysis of sequences published as examples of the second type of rearrangement. This not only shows that AID recognition motifs occur in recombination regions but also that some sequences show replacement of central sections by a sequence from another gene, similar to gene conversion in the immunoglobulin genes of other species. These observations support the proposal that this type of rearrangement is likely to be AID-mediated rather than RAG-mediated and is consistent with gene conversion.
在过去20年里,许多DNA序列已被公布,这表明重排免疫球蛋白基因的全部或部分V(H)区段可能在体内被替换。似乎有两种不同的机制在起作用。其中一种与原发性V(D)J重组非常相似,涉及作用于重组信号序列的RAG蛋白,并且最近已被证实会发生。其他序列,其中许多在V(H)-V(H)连接处显示部分V(H)替换且未添加非模板化核苷酸,有人提出是通过一种不寻常的RAG介导的重组并形成杂种(编码到信号)接头而发生的。这些似乎发生在已经经历体细胞超突变的细胞中,一些作者确信,在这些细胞中RAG基因是沉默的。我们最近提出,后一种类型的V(H)替换可能是由AID(激活诱导的胞苷脱氨酶)的活性引发的同源重组导致的,AID对于体细胞超突变和基因转换至关重要。后者在其他物种中已被观察到,但迄今为止在人类Ig基因中尚未观察到。在本文中,我们对作为第二种重排类型示例而发表的序列进行了新的分析。这不仅表明AID识别基序出现在重组区域,而且还表明一些序列显示中央部分被来自另一个基因的序列所取代,这类似于其他物种免疫球蛋白基因中的基因转换。这些观察结果支持了这样的提议,即这种重排类型可能是由AID介导而非RAG介导的,并且与基因转换一致。