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[急性白血病患儿重链免疫球蛋白基因及T细胞受体δ基因分析]

[Analysis of heavy chain immunoglobulins gene and T-cell receptor delta gene in children with acute leukemia].

作者信息

Pan Q, Chou Y, Hong W

机构信息

Affiliated Children's Hospital, Zhejiang Medical University, Hangzhou.

出版信息

Zhonghua Yi Xue Za Zhi. 1995 Sep;75(9):529-31, 573.

PMID:8556542
Abstract

IgH gene, TCR delta gene rearrangements and Tal-1 gene deletion were analysed by using PCR, Southern blot and DNA sequencing methods in newly diagnosed BM samples from children with AL. The DNAs from leukemic cells in 102 children were detected with PCR. The results showed that IgH gene rearrangement mainly occurred in B Precursor ALL (37/49). Six PCR products were further analysed by DNA sequencing. Less homogene and bias of JH gene usage were found in analysed DNA sequences. V delta 2-D delta 3 rearrangement of 78 samples from ALL was analysed with PCR method. V delta 2-D delta 3 rearrangements mainly observed in B precursor ALL and related HAL. V delta 2-D delta 2-N-D delta 3 rearrangement was found in a sequence of PCR product. Three cases of Tal-1 gene deletion were observed in all studied 70 samples of AL. They all were in stage I of thymus differentiation. We conclud that PCR detection of those genes are useful in the diagnosis of clonality of AL, DNA sequencing of PCR products is the base of preparing clonal specific probes, and dynamic analysis of IgH gene rearrangement using PCR may be helpful in detection of residual clones.

摘要

采用聚合酶链反应(PCR)、Southern印迹和DNA测序方法,对新诊断的儿童急性白血病(AL)骨髓样本中的免疫球蛋白重链(IgH)基因、T细胞受体δ(TCR delta)基因重排以及Tal-1基因缺失情况进行了分析。用PCR检测了102例儿童白血病细胞的DNA。结果显示,IgH基因重排主要发生在B系前体急性淋巴细胞白血病(B Precursor ALL,37/49)。对6个PCR产物进一步进行DNA测序分析,在分析的DNA序列中发现JH基因使用的同源性较低且存在偏差。采用PCR方法分析了78例急性淋巴细胞白血病(ALL)样本的Vδ2-Dδ3重排。Vδ2-Dδ3重排主要见于B系前体ALL及相关的混合性急性白血病(HAL)。在一个PCR产物序列中发现了Vδ2-Dδ2-N-Dδ3重排。在所有研究的70例AL样本中观察到3例Tal-1基因缺失,它们均处于胸腺分化I期。我们得出结论,对这些基因进行PCR检测有助于诊断AL的克隆性,PCR产物的DNA测序是制备克隆特异性探针的基础,采用PCR对IgH基因重排进行动态分析可能有助于检测残留克隆。

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