Heilig J S, Tonegawa S
Center for Cancer Research, Massachusetts Institute of Technology, Cambridge 02139.
Proc Natl Acad Sci U S A. 1987 Nov;84(22):8070-4. doi: 10.1073/pnas.84.22.8070.
The T-cell gamma genes, structurally related to immunoglobulin genes and the T-cell antigen-receptor alpha- and beta-chain genes, undergo somatic rearrangement in T-lineage cells. However, the role of the T-cell gamma genes has not yet been determined. To determine the potential for gamma gene expression in a set of well-characterized, cloned T-cell lines, we cloned all of the rearranged gamma genes from each cell line. The genes were sequenced to determine if the junction of the variable and joining regions maintained the proper translational reading frame. We then attempted to correlate the presence of an in-frame gamma gene with a T-cell subset. We were unable to establish such a correlation. We found evidence, however, that allelic exclusion influences the rearrangement of the gamma gene. This is consistent with the idea that the gamma gene product participates in establishing a clonally diverse population of T cells recognizing a polymorphic ligand. Isotypic exclusion does not apply to the gamma gene, however, suggesting different roles for the different gamma gene isotypes.
T细胞γ基因在结构上与免疫球蛋白基因以及T细胞抗原受体α链和β链基因相关,在T系细胞中经历体细胞重排。然而,T细胞γ基因的作用尚未确定。为了确定一组特征明确的克隆T细胞系中γ基因表达的潜力,我们从每个细胞系中克隆了所有重排的γ基因。对这些基因进行测序,以确定可变区和连接区的连接处是否保持正确的翻译阅读框。然后,我们试图将框内γ基因的存在与T细胞亚群相关联。我们未能建立起这种关联。然而,我们发现有证据表明等位基因排斥会影响γ基因的重排。这与γ基因产物参与建立识别多态性配体的克隆性多样化T细胞群体的观点一致。然而,同种型排斥不适用于γ基因,这表明不同的γ基因同种型具有不同的作用。