Kidd Marie J, Jackson Katherine J L, Boyd Scott D, Collins Andrew M
School of Biotechnology and Biomolecular Sciences, University of New South Wales, Kensington, Sydney, New South Wales 2052, Australia; and.
School of Biotechnology and Biomolecular Sciences, University of New South Wales, Kensington, Sydney, New South Wales 2052, Australia; and Department of Pathology, Stanford University, Stanford, CA 94305.
J Immunol. 2016 Feb 1;196(3):1158-64. doi: 10.4049/jimmunol.1501401. Epub 2015 Dec 23.
Human IgH diversity is influenced by biases in the pairing of IGHD and IGHJ genes, but these biases have not been described in detail. We used high-throughput sequencing of VDJ rearrangements to explore DJ pairing biases in 29 individuals. It was possible to infer three contrasting IGHD-IGHJ haplotypes in nine of these individuals, and two of these haplotypes include deletion polymorphisms involving multiple contiguous IGHD genes. Therefore, we were able to explore how the underlying genetic makeup of the H chain locus influences the formation of particular DJ pairs. Analysis of nonproductive rearrangements demonstrates that 3' IGHD genes tend to pair preferentially with 5' IGHJ genes, whereas 5' IGHD genes pair preferentially with 3' IGHJ genes; the relationship between IGHD gene pairing frequencies and IGHD gene position is a near linear one for each IGHJ gene. However, striking differences are seen in individuals who carry deletion polymorphisms in the D locus. The absence of different blocks of IGHD genes leads to increases in the utilization frequencies of just a handful of genes, and these genes have no clear positional relationships to the deleted genes. This suggests that pairing frequencies may be influenced by additional complex positional relationships that perhaps arise from chromatin structure. In contrast to IGHD gene usage, IGHJ gene usage is unaffected by the IGHD gene-deletion polymorphisms. Such an outcome would be expected if the recombinase complex associates with an IGHJ gene before associating with an IGHD gene partner.
人类免疫球蛋白重链(IgH)的多样性受免疫球蛋白重链多样性基因(IGHD)和免疫球蛋白重链连接基因(IGHJ)配对偏差的影响,但这些偏差尚未得到详细描述。我们利用VDJ重排的高通量测序技术,对29名个体的DJ配对偏差进行了探究。在其中9名个体中,有可能推断出三种截然不同的IGHD-IGHJ单倍型,其中两种单倍型包含涉及多个相邻IGHD基因的缺失多态性。因此,我们能够探究重链基因座的潜在基因组成如何影响特定DJ对的形成。对无功能重排的分析表明,3'端的IGHD基因倾向于优先与5'端的IGHJ基因配对,而5'端的IGHD基因则优先与3'端的IGHJ基因配对;对于每个IGHJ基因,IGHD基因配对频率与IGHD基因位置之间的关系近乎呈线性。然而,在D基因座携带缺失多态性的个体中,观察到了显著差异。不同IGHD基因块的缺失导致仅少数基因的利用频率增加,并且这些基因与缺失基因没有明确的位置关系。这表明配对频率可能受染色质结构可能产生的其他复杂位置关系的影响。与IGHD基因的使用情况不同,IGHJ基因的使用不受IGHD基因缺失多态性的影响。如果重组酶复合物在与IGHD基因伴侣结合之前先与IGHJ基因结合,那么这样的结果是可以预期的。