Koop B F, Rowen L, Wang K, Kuo C L, Seto D, Lenstra J A, Howard S, Shan W, Deshpande P, Hood L
Department of Biology, University of Victoria, British Columbia, Canada.
Genomics. 1994 Feb;19(3):478-93. doi: 10.1006/geno.1994.1097.
We sequenced and analyzed 97.6 kb of new DNA sequence containing the human TCRAC (C alpha) and TCRDC (C delta) genes as well as the TCRDV3 (V delta 3) and 61 different TCRAJ (J alpha) gene segments and compared its organization and structure to the previously described mouse T-cell receptor TCRAC/TCRDC (C alpha/C delta) region. A comprehensive nomenclature, consistent with the IUIS nomenclature committee recommendations, for both human and mouse TCRAJ gene segments is presented. In the human sequence, we identified 20 new TCRAJ gene segments and obtained the germline sequence for 23 additional TCRAJ gene segments known from cDNA clones. Using the sequence data obtained from the human TCRAC/TCRDC region, we have extended a polymerase chain reaction-based assay to test for the expression of the individual TCRAJ gene segments. At least five TCRAJ pseudogene segments were identified by sequence criteria. Like the murine TCRAC/TCRDC sequence, this sequence contains a high level of coding sequence, with over 6.6% of the total sequence being transcribed. Comparison of the human sequence with the previously reported mouse DNA sequence reveals homologous counterparts for the variable and joining (J) gene segments and both constant genes. Eleven new J pseudogene segments have been identified in the mouse TCRAC/TCRDC sequence through the use of human and mouse sequence comparisons. In terms of structure and organization, this region of the human and mouse genome appears to be remarkably conserved.
我们对包含人类TCRAC(Cα)和TCRDC(Cδ)基因以及TCRDV3(Vδ3)和61个不同的TCRAJ(Jα)基因片段的97.6 kb新DNA序列进行了测序和分析,并将其组织和结构与先前描述的小鼠T细胞受体TCRAC/TCRDC(Cα/Cδ)区域进行了比较。提出了一套与国际免疫学会命名委员会建议一致的人类和小鼠TCRAJ基因片段的综合命名法。在人类序列中,我们鉴定出20个新的TCRAJ基因片段,并获得了另外23个从cDNA克隆中已知的TCRAJ基因片段的种系序列。利用从人类TCRAC/TCRDC区域获得的序列数据,我们扩展了一种基于聚合酶链反应的检测方法,以检测各个TCRAJ基因片段的表达。通过序列标准鉴定出至少五个TCRAJ假基因片段。与小鼠TCRAC/TCRDC序列一样, 该序列包含高水平的编码序列,总序列中有超过6.6%被转录。将人类序列与先前报道的小鼠DNA序列进行比较,发现可变区和连接(J)基因片段以及两个恒定基因都有同源对应物。通过人类和小鼠序列比较,在小鼠TCRAC/TCRDC序列中鉴定出11个新的J假基因片段。在结构和组织方面,人类和小鼠基因组的这一区域似乎非常保守。