Kuang S, Dong S, Gu L
Shanghai Institute of Hematology, Ruijin Hospital, Shanghai Second Medical University.
Zhonghua Yi Xue Za Zhi. 1995 Sep;75(9):532-6, 574.
T-cell receptor (TCR) delta chain gene rearrangements were studied by polymerase chain reaction (PCR) analysis in 46 patients with acute lymphoblastic leukemia (ALL). Sixteen patients were found to have incomplete rearrangements of the TCR delta genes. Among them, 13 patients displayed V delta 2-D delta 3 rearrangement, while 3 had both V delta 2-D delta 3 and D delta 2-D delta 3 rearrangements. To determine the junctional sequence of TCR delta gene, PCR products from the 16 patients were sequenced directly or after M13 cloning. The results showed the junctional sequences of TCR delta gene are highly specific for each allele. This sequence diversity resulted from several factors including deletion of the 3' end of V delta 2 or D delta 2 segment and 5' end of D delta 3 segment, the presence of D delta 1 or D delta 2 sequences, insertion of N nucleotides and the association of P nucleotides with intact V delta 2 and D delta 3 segments. In addition, analysis of N-nucleotide contents revealed that the amount of GC was much larger than that of AT (70%: 30%), indicating the insertion of N nucleotide was not fully random. Our sequence data confirmed that the imcomplete rearrangement of TCR delta gene is an early event in the lymphoid cell ontogenesis, and its N sequences in V-(D)-J junctional region may be used as a specific marker of clonality to detect the minimal residual disease (MRD) in ALL.
通过聚合酶链反应(PCR)分析,对46例急性淋巴细胞白血病(ALL)患者的T细胞受体(TCR)δ链基因重排进行了研究。发现16例患者存在TCRδ基因的不完全重排。其中,13例患者表现为Vδ2-Dδ3重排,3例同时存在Vδ2-Dδ3和Dδ2-Dδ3重排。为确定TCRδ基因的连接序列,对这16例患者的PCR产物直接测序或经M13克隆后测序。结果显示,TCRδ基因的连接序列对每个等位基因具有高度特异性。这种序列多样性由多种因素导致,包括Vδ2或Dδ2片段3'端以及Dδ3片段5'端的缺失、Dδ1或Dδ2序列的存在、N核苷酸的插入以及P核苷酸与完整Vδ2和Dδ3片段的关联。此外,对N核苷酸含量的分析表明,GC的含量远高于AT(70%:30%),这表明N核苷酸的插入并非完全随机。我们的序列数据证实,TCRδ基因的不完全重排是淋巴细胞个体发育中的早期事件,其V-(D)-J连接区的N序列可作为检测ALL微小残留病(MRD)的克隆性特异性标志物。