Mahotka C, Hansen-Hagge T E, Bartram C R
Department of Pediatrics II, University of Ulm, Germany.
Leukemia. 1995 Oct;9(10):1700-3.
Human acute lymphoblastic leukemia cell lines represent valuable tools to investigate distinct steps of the complex regulatory pathways underlying T cell receptor recombination and expression. A case in point are V delta 2D delta 3 and subsequent V delta 2D delta 3J alpha rearrangements observed in human leukemic pre-B cells as well as in normal lymphopoiesis. The functional expression of these unusual (VD) delta (JC) alpha hybrids is almost exclusively prevented by alternative splicing events. In this report we show that alternative splicing at cryptic splice donor sites within V elements is not a unique feature of hybrid TCR delta/alpha transcripts. Among seven V alpha families analyzed by RT-PCR, alternatively spliced products were observed in TCR alpha recombinations containing V alpha 1 or V alpha 14 elements. In contrast to normal peripheral blood cells and thymocytes, the leukemia cell line JM expressing functional V alpha 1J alpha 3C alpha transcripts lacked evidence of aberrant TCR alpha RNA species.
人类急性淋巴细胞白血病细胞系是研究T细胞受体重组和表达背后复杂调控途径不同步骤的宝贵工具。一个恰当的例子是在人类白血病前B细胞以及正常淋巴细胞生成过程中观察到的Vδ2Dδ3和随后的Vδ2Dδ3Jα重排。这些不寻常的(VD)δ(JC)α杂种的功能表达几乎完全被可变剪接事件所阻止。在本报告中,我们表明V元件内隐蔽剪接供体位点的可变剪接并非杂交TCRδ/α转录本的独特特征。通过RT-PCR分析的七个Vα家族中,在包含Vα1或Vα14元件的TCRα重组中观察到了可变剪接产物。与正常外周血细胞和胸腺细胞不同,表达功能性Vα1Jα3Cα转录本的白血病细胞系JM没有异常TCRαRNA种类的证据。