Davodeau F, Peyrat M A, Hallet M M, Vié H, Bonneville M
INSERM U211, Biology Institute, Nantes, France.
J Immunol. 1994 Jul 1;153(1):137-42.
Through analysis of TCR delta-chain cDNA derived from human gamma delta T cell clones and polyclonal gamma delta T cell lines, we isolated a novel functional J delta gene segment (termed J delta 4) whose genomic fragment has been mapped within the TCR-delta locus between J delta 2 and J delta 1. Frequency of J delta 4 use was estimated among adult gamma delta PBL by using V delta 1, V delta 2, and V delta 5 genes. In all cases, this new J element was used at a low, albeit significant frequency, close to that of J delta 2. Finally, like human J delta 1 and J delta 2, which show a high degree of homology with their counterparts in the mouse and sheep, but unlike other J gamma, J beta, or J alpha elements, J delta 4 turned out to be highly homologous to a recently described ovine J delta. These results suggest the existence of strong selective pressures, possibly linked to an Ag-driven process, leading to specific conservation of J delta sequences among these three species.
通过对源自人γδ T细胞克隆和多克隆γδ T细胞系的TCR δ链cDNA进行分析,我们分离出了一个新的功能性Jδ基因片段(称为Jδ4),其基因组片段已定位在TCR-δ基因座中Jδ2和Jδ1之间。通过使用Vδ1、Vδ2和Vδ5基因,估计了成人γδ外周血淋巴细胞中Jδ4的使用频率。在所有情况下,这个新的J元件虽使用频率较低,但具有统计学意义,接近Jδ2的使用频率。最后,如同人Jδ1和Jδ2与小鼠和绵羊中的对应物具有高度同源性一样,但与其他Jγ、Jβ或Jα元件不同,Jδ4与最近描述的绵羊Jδ高度同源。这些结果表明存在强大的选择压力,可能与抗原驱动的过程有关,导致这三个物种之间Jδ序列的特异性保守。