Rothenfluh H S, Taylor L, Bothwell A L, Both G W, Steele E J
Department of Biological Sciences, University of Wollongong, NSW, Australia.
Eur J Immunol. 1993 Sep;23(9):2152-9. doi: 10.1002/eji.1830230916.
The aim of this study has been to determine the distribution of somatic mutations in the 5' flanking regions of rearranged immunoglobulin heavy chain variable region genes (VDJ). We sequenced the 5' flanking region in 12 secondary immune response antibodies produced in C57BL/6j mice against the hapten (4-hydroxy-3-nitrophenyl)acetyl (NP) coupled to chicken-gamma-globulin. In these and previously published sequences, almost 97% of the mutations occurred in the transcribed region of the gene, and only a minority of genes (5/29) contained mutations upstream of the transcription start (cap) site. No potential germ-line donor was found for a cluster of five base changes previously found in a single heavy chain gene, 3B62. However, the uniqueness of this mutational cluster and its distance from the normally mutated region suggests that the nucleotide changes may not be due to the normal mutator mechanism. Thus, as this was the only instance of somatic mutations that far upstream of the promoter/cap site region, the reverse transcriptase model for somatic hypermutation is still a possibility. The data are consistent with a mutational mechanism that requires transcription of the rearranged target V(D)J gene which appears to result in the generation of a positively skewed asymmetrical distribution of somatic mutations. A single mode is centered near the V(D)J and a long tail extends into the 3' non-translated region of the J-C intron. Two classes of model could explain this mutation distribution pattern: those where transcription products (RNA, cDNA) are the direct mutational substrates, or those that postulate local unfolding of the chromatin around a V(D)J rearrangement directly exposing the DNA of the transcribed region to specific mutational enzymes.
本研究的目的是确定重排的免疫球蛋白重链可变区基因(VDJ)5'侧翼区域体细胞突变的分布。我们对C57BL/6j小鼠产生的针对与鸡γ球蛋白偶联的半抗原(4-羟基-3-硝基苯基)乙酰基(NP)的12种二次免疫应答抗体的5'侧翼区域进行了测序。在这些序列以及先前发表的序列中,几乎97%的突变发生在基因的转录区域,只有少数基因(5/29)在转录起始(帽)位点上游含有突变。对于先前在单个重链基因3B62中发现的一组五个碱基变化,未找到潜在的种系供体。然而,这个突变簇的独特性及其与正常突变区域的距离表明,核苷酸变化可能不是由于正常的诱变机制。因此,由于这是启动子/帽位点区域上游如此远的位置出现体细胞突变的唯一实例,体细胞超突变的逆转录酶模型仍然是一种可能性。数据与一种突变机制一致,该机制需要重排的目标V(D)J基因转录,这似乎导致体细胞突变产生正偏态不对称分布。一个单一模式集中在V(D)J附近,一条长尾巴延伸到J-C内含子的3'非翻译区域。两类模型可以解释这种突变分布模式:一类是转录产物(RNA、cDNA)是直接的突变底物,另一类假设V(D)J重排周围的染色质局部解折叠,直接将转录区域的DNA暴露于特定的突变酶。