Le Beau M M, McKeithan T W, Shima E A, Goldman-Leikin R E, Chan S J, Bell G I, Rowley J D, Diaz M O
Proc Natl Acad Sci U S A. 1986 Dec;83(24):9744-8. doi: 10.1073/pnas.83.24.9744.
Chromosomal rearrangements in malignant T-cell disease frequently involve the chromosome bands containing the T-cell receptor genes. The RPMI 8402 cell line, which was established from the leukemia cells of a patient with T-cell acute lymphoblastic leukemia, is characterized by a translocation involving chromosome 14 (band q11) and chromosome 11 (band p15) [t(11;14)(p15;q11)]. By using in situ chromosomal hybridization and Southern blot analysis to examine RPMI 8402 cells, we determined that the break at 14q11 occurs within the variable region sequences of the T-cell receptor alpha-chain gene (TCRA); the break at 11p15 occurs between the HRAS1 gene and the genes for insulin and the insulin-like growth factor 2. These results suggest that the TCRA sequences activate a cellular gene located at 11p15 in malignant T-cell disorders.
恶性T细胞疾病中的染色体重排常常涉及包含T细胞受体基因的染色体带。RPMI 8402细胞系是从一名T细胞急性淋巴细胞白血病患者的白血病细胞中建立的,其特征是涉及14号染色体(q11带)和11号染色体(p15带)的易位[t(11;14)(p15;q11)]。通过使用原位染色体杂交和Southern印迹分析来检测RPMI 8402细胞,我们确定14q11处的断裂发生在T细胞受体α链基因(TCRA)的可变区序列内;11p15处的断裂发生在HRAS1基因与胰岛素及胰岛素样生长因子2的基因之间。这些结果表明,在恶性T细胞疾病中,TCRA序列激活了位于11p15的一个细胞基因。