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儿童急性白血病T细胞受体δ、γ基因重排连接区序列的动态分析
引用本文:卢洁,谷仁凯,雷珂.儿童急性白血病T细胞受体δ、γ基因重排连接区序列的动态分析[J].中华血液学杂志,2000,21(6):301-304.
作者姓名:卢洁  谷仁凯  雷珂
作者单位:青岛大学医学院附属医院儿科研究所
基金项目:山东省自然科学基金资助项目!(Y97C170 5 3 ),山东省“九五”医药科技攻关资助项目!(鲁卫科教字 [1997]第九号 )
摘    要:目的 探讨儿童急性淋巴细胞白血病(ALL)患在初诊、完全缓解(CR)及复发不同时期的T细胞3受体(TCR)δV-D,γV-J基因重排连接区序列的差异及其意义。方法 采用T-载体分子克隆测离1限制性酶团及聚合酶链反应等技术,对34丛ALL患标本进行TCTδ、γ连接区序列动态分析。结果 34丛ALL患标本进行TCR-5γ连接区序列动态分析。结果 34份ALL患标本的TCR5、γ基因重排序列在初

关 键 词:急性白血病  T细胞受体  分子克隆  基因重排

Dynamic analysis of junctional sequences of T cell receptor (TCR) delta and gamma gene rearrangement in childhood with acute lymphoblastic leukemia]
LU Jie,GU Renkai,LEI Ke,et al..Dynamic analysis of junctional sequences of T cell receptor (TCR) delta and gamma gene rearrangement in childhood with acute lymphoblastic leukemia][J].Chinese Journal of Hematology,2000,21(6):301-304.
Authors:LU Jie  GU Renkai  LEI Ke  
Institution:Institute of Pediatrics, Affiliated Hospital, Medical School of Qingdao University, Qingdao 266003, China.
Abstract:OBJECTIVE: To explore the junctional sequence difference of T cell receptor delta and gamma gene rearrangement in childhood acute lymphoblastic leukemia (ALL) at diagnosis, complete remission (CR) and relapse. METHODS: By using the T-vector molecular cloning and sequencing and polymerase chain reaction, the junctional sequences of TCRdeltaV-D and TCRgammaV-J were dynamically analyzed in 34 bone marrow samples of ALL. RESULTS: The junctional sequence of TCR delta, gamma gene showed significant difference and regularity before and after remission and during relapsed periods. The sequence of TCRdeltaV-D were analyzed in 24 samples from ALL. Among them, the intact Vdelta2 and 5'Ddelta3 sequences were observed in 10 samples at diagnosis, of which 7 samples had T-->C mutation in Ddelta3 nonamer sequence. The deletions of rearranged Vdelta2, 5'Ddelta3 and Ddelta3 haptamer sequences were found in 11 complete remission (CR) samples with ALL, but none had T-->C mutation in Ddelta3 nonamer sequence. The deletion rate of Vdelta2 or Ddelta3 sequences and the T-->C mutation in Ddelta3 nonamer sequence were extremely differed between samples at diagnosis and in remission (calculate exact probabilities P = 0.001). The junctional rearrangement sequence of 5'Ddelta3 sequences tended to remain intact in 3 relapsed samples. The findings of TCRgammaV-J sequences were similar to that of TCRdeltaV-D in 10 ALL patients. CONCLUSION: The difference of TCRdeltaV-D and TCRgammaV-J junctional sequences were related to the development, therapeutic effectiveness and outcome in ALL.
Keywords:Leukemia  acute  T cell receptor  Molecular cloning  Dynamic sequence analysis
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