Kenter A L
Department of Microbiology and Immunology, University of Illinois College of Medicine, Chicago 60612-7344, USA.
Curr Top Microbiol Immunol. 2005;290:171-99. doi: 10.1007/3-540-26363-2_8.
Class switch recombination (CSR) has been the least well understood of the Ig gene DNA rearrangements. The discovery that activation-induced deaminase (AID) is a pivotal player in CSR as well as somatic hypermutation (SHM) and its variant, gene conversion, represents a sea change in our understanding of these processes. The recognition that AID directly deaminates ssDNA has provided a springboard toward the emergence of a model that explains the initiation of these events. Nonhomologous end joining (NHEJ), the main pathway for the repair of double-strand breaks in mammalian cells plays a key role in the resolution of CSR transactions. Mediators of general double-strand break repair are also involved in CSR and are mutated in several immunodeficiency diseases. A global picture of the mechanism of CSR is emerging and is providing new insights toward understanding the genetic events that underlie B cell cancers.
类别转换重组(CSR)是免疫球蛋白(Ig)基因DNA重排中最不为人所理解的过程。激活诱导的脱氨酶(AID)在CSR以及体细胞高频突变(SHM)及其变体基因转换中起关键作用,这一发现代表了我们对这些过程理解的巨大转变。认识到AID直接使单链DNA脱氨基,为解释这些事件起始的模型的出现提供了跳板。非同源末端连接(NHEJ)是哺乳动物细胞中双链断裂修复的主要途径,在CSR过程的解决中起关键作用。一般双链断裂修复的介导因子也参与CSR,并且在几种免疫缺陷疾病中发生突变。CSR机制的整体图景正在浮现,并为理解B细胞癌的遗传事件提供了新的见解。