Harriman W, Völk H, Defranoux N, Wabl M
Department of Microbiology and Immunology, University of California, San Francisco 94143-0670.
Annu Rev Immunol. 1993;11:361-84. doi: 10.1146/annurev.iy.11.040193.002045.
A B lymphocyte that produces the immunoglobulin heavy (H) chain mu may switch to the production of another heavy chain class: gamma, epsilon, or alpha. Since the new heavy chain retains the original variable (V) region, antigenic specificity is maintained. The switch is accompanied by a large deletion of DNA at the heavy chain locus. To explain how this deletion is generated, three models have been proposed: recombination between homologs, unequal sister chromatid exchange, and looping out and deletion. While none of the predicted recombination products of the first two models have been found, both by-products of looping out--inversions and circular DNA--have been isolated. Thus looping out and deletion appears to be the appropriate model to explain the genetic events leading to the immunoglobulin heavy chain class switch. One requirement for switching may be transcription of the constant (C) region to which the cell switches. The switch rearrangement is catalyzed by a switch recombinase, and the isolation of the components of this putative enzyme system is in progress. Although the switch deletion is an accepted fact, the discussion is enlivened by scenarios for switching without DNA rearrangement; such suggestions include processing at the RNA level and trans-splicing.
产生免疫球蛋白重链(H链)μ的B淋巴细胞可能会转而产生另一种重链类别:γ、ε或α。由于新的重链保留了原来的可变(V)区,抗原特异性得以维持。这种转换伴随着重链基因座处大量DNA的缺失。为了解释这种缺失是如何产生的,人们提出了三种模型:同源物之间的重组、不等姐妹染色单体交换以及环出和缺失。虽然前两种模型预测的重组产物均未被发现,但环出的两种副产物——倒位和环状DNA——已被分离出来。因此,环出和缺失似乎是解释导致免疫球蛋白重链类别转换的遗传事件的合适模型。转换的一个条件可能是细胞所转换的恒定(C)区的转录。转换重排由一种转换重组酶催化,目前正在对这种假定酶系统的成分进行分离。尽管转换缺失是一个公认的事实,但关于无DNA重排的转换情形的讨论仍很热烈;这些建议包括RNA水平的加工和反式剪接。