Mami-Chouaib F, Jitsukawa S, Faure F, Vasina B, Genevee C, Hercend T, Triebel F
Laboratoire d'Immunologie Cellulaire, Institut Gustave-Roussy, Villejuif, France.
Eur J Immunol. 1989 Sep;19(9):1545-9. doi: 10.1002/eji.1830190905.
We have identified in earlier studies two V delta rearrangements corresponding to a 4.5-kb Eco RI fragment detected with a V delta1 probe and to a 7-kb Eco RI band detected with a V delta2 probe. These rearrangements have been found in two human T cell clones, F6C7 and G6, displaying surface phenotypes unfrequent in human peripheral blood, namely Ti gamma A+ BB3- (F6C7) and Ti gamma A- BB3+ (G6). Herein, we report the sequences of the functional transcripts encoded by these rearranged genes and show that the 4.5- and the 7-kb Eco RI fragments correspond to V1/D3/J delta 3 and to V2/D3/J delta 3 recombinations, respectively. In addition, we have sequenced the V2/D3/J1/C delta transcripts expressed in two clones, AB12 and VTC, which have a Ti gamma A+ BB3+ surface phenotype corresponding to that of most gamma/delta peripheral lymphocytes. Analyses of the delta transcripts expressed by these four cells further strengthen the hypothesis that anti-BB3 and anti-delta-TCS-1 monoclonal antibodies recognize a V delta 2- and a V1/(D)/J delta 1-encoded epitope, respectively. Sequence of the gamma transcripts expressed by AB12 and F6C7 cells shows that they encode a V9/JP/C gamma 1 chain. Finally, we confirm that non-combinatorial diversity in the gamma and delta proteins is generated by both junctional flexibility and N-region addition without any somatic mutation.
我们在早期研究中鉴定出两种Vδ重排,一种对应于用Vδ1探针检测到的4.5kb Eco RI片段,另一种对应于用Vδ2探针检测到的7kb Eco RI条带。这些重排在两个人类T细胞克隆F6C7和G6中被发现,它们表现出人类外周血中不常见的表面表型,即TiγA + BB3 - (F6C7)和TiγA - BB3 + (G6)。在此,我们报告了这些重排基因编码的功能性转录本的序列,并表明4.5kb和7kb的Eco RI片段分别对应于V1/D3/Jδ3和V2/D3/Jδ3重组。此外,我们对在两个克隆AB12和VTC中表达的V2/D3/J1/Cδ转录本进行了测序,这两个克隆具有与大多数γ/δ外周淋巴细胞相对应的TiγA + BB3 + 表面表型。对这四个细胞表达的δ转录本的分析进一步强化了这样的假设,即抗BB3和抗δ-TCS-1单克隆抗体分别识别一个由Vδ2和V1/(D)/Jδ1编码的表位。AB12和F6C7细胞表达的γ转录本序列表明它们编码一条V9/JP/Cγ1链。最后,我们证实γ和δ蛋白中的非组合多样性是由连接灵活性和N区添加产生的,没有任何体细胞突变。