Yang Shu Yuan, Schatz David G
Section of Immunobiology, Yale University School of Medicine, New Haven, Connecticut, USA.
Adv Immunol. 2007;94:109-25. doi: 10.1016/S0065-2776(06)94004-8.
After their assembly by V(D)J recombination, immunoglobulin (Ig) genes undergo somatic hypermutation, gene conversion, and class switch recombination to generate additional antibody diversity. The three diversification processes depend on activation-induced cytidine deaminase (AID) and are tightly linked to transcription. The reactions occur primarily on Ig genes and the molecular mechanisms that underlie their targeting to Ig loci have been of intense interest. In this chapter, we discuss the evidence linking transcription and transcriptional control elements to the three diversification pathways, and we consider how various features of chromatin could render parts of the genome permissive for AID-mediated sequence diversification.
通过V(D)J重排组装后,免疫球蛋白(Ig)基因经历体细胞超突变、基因转换和类别转换重排,以产生额外的抗体多样性。这三种多样化过程依赖于激活诱导的胞苷脱氨酶(AID),并与转录紧密相连。这些反应主要发生在Ig基因上,其靶向Ig基因座的分子机制一直备受关注。在本章中,我们讨论了将转录和转录控制元件与这三种多样化途径联系起来的证据,并思考了染色质的各种特征如何使基因组的某些部分允许AID介导的序列多样化。