Genevée C, Chung V, Diu A, Hercend T, Triebel F
Laboratoire d'Immunologie Cellulaire, INSERM U333, Institut Gustave-Roussy, Villejuif, France.
Mol Immunol. 1994 Feb;31(2):109-15. doi: 10.1016/0161-5890(94)90083-3.
Using PCR and an experimentally validated V alpha subfamily-specific oligonucleotide panel (V alpha 1-w29), we have investigated whether the TCR delta chain may increase its combinatorial diversity by using V genes considered as alpha chain-specific. We show that at least 10 distinct human V alpha segments rearrange at the J delta locus, leading to scrambling of the two V gene repertoires. Fifty-five per cent of the V alpha/J delta transcripts characterized here were in frame. The 17 V alpha/C delta chains analysed included an extended CDR3 region with up to 18 aa encoded by the junctional region. In addition, a new J delta segment (J delta 4) has been characterized. Together, these findings demonstrate that combinatorial diversity in the human delta locus is larger than previously thought.
利用聚合酶链反应(PCR)和经过实验验证的Vα亚家族特异性寡核苷酸组(Vα1-w29),我们研究了T细胞受体δ链是否可通过使用被认为是α链特异性的V基因来增加其组合多样性。我们发现至少有10个不同的人类Vα片段在Jδ基因座处重排,导致两个V基因库的混杂。在此表征的Vα/Jδ转录本中有55%是读框内的。所分析的17条Vα/Cδ链包含一个扩展的互补决定区3(CDR3)区域,其由连接区编码的氨基酸多达18个。此外,一个新的Jδ片段(Jδ4)已被表征。总之,这些发现表明人类δ基因座中的组合多样性比之前认为的要大。