Chen Q, Cheng J T, Tasi L H, Schneider N, Buchanan G, Carroll A, Crist W, Ozanne B, Siciliano M J, Baer R
Department of Microbiology, University of Texas Southwestern Medical Center, Dallas 75235.
EMBO J. 1990 Feb;9(2):415-24. doi: 10.1002/j.1460-2075.1990.tb08126.x.
We have analyzed t(1;14)(p32;q11) chromosome translocations from two patients with T cell acute lymphocytic leukemia. The chromosome 1 breakpoints of these patients lie within a kilobasepair of each other, and thus define a genetic locus (designated tal) involved in T cell oncogenesis. Moreover, we have identified sequences within tal that potentially encode an amphipathic helix-loop-helix motif, a DNA-binding domain found in a variety of proteins that control cell growth and differentiation. The homology domain of tal is especially related to that of lyl-1, a gene on chromosome 19 that has also been implicated in T cell oncogenesis. Hence, tal and lyl-1 encode a distinct family of helix-loop-helix proteins involved in the malignant development of lymphocytes.
我们分析了两名T细胞急性淋巴细胞白血病患者的t(1;14)(p32;q11)染色体易位情况。这两名患者的1号染色体断点彼此相距在1千碱基对内,因此确定了一个参与T细胞肿瘤发生的基因位点(命名为tal)。此外,我们在tal中鉴定出了可能编码两亲性螺旋-环-螺旋基序的序列,这是一种在多种控制细胞生长和分化的蛋白质中发现的DNA结合结构域。tal的同源结构域与19号染色体上的lyl-1基因的同源结构域特别相关,lyl-1基因也与T细胞肿瘤发生有关。因此,tal和lyl-1编码了一个参与淋巴细胞恶性发育的独特的螺旋-环-螺旋蛋白家族。