Tkachuk D C, Kohler S, Cleary M L
Department of Pathology, Stanford University School of Medicine, California 94305.
Cell. 1992 Nov 13;71(4):691-700. doi: 10.1016/0092-8674(92)90602-9.
We have identified a human homolog of the Drosophila trithorax protein that is structurally altered by 11q23 translocations in acute leukemias. Human trithorax (HRX) is a predicted 431 kd protein containing two potential DNA-binding motifs consisting of zinc fingers conserved with the fly protein and nonconserved amino-terminal "AT hook" motifs related to the DNA-binding motifs in HMG proteins. 11q23 translocations disrupt the HRX gene between these two motifs, and in a t(11;19)-carrying cell line fusion transcripts are expressed from both derivative chromosomes. The more abundant derivative 11 transcript codes for a chimeric protein containing the AT hook motifs fused to a previously undescribed protein (ENL) from chromosome 19. These data suggest a novel role for a trithorax-homologous protein in multilineage human leukemias that may be mediated by DNA binding within the minor groove at AT-rich sites, implicated to play an important role in bacterial IHF-, yeast datin-, and mammalian HMG-mediated gene activation.
我们已经鉴定出果蝇三体胸蛋白的一种人类同源物,该同源物在急性白血病中因11q23易位而发生结构改变。人类三体胸蛋白(HRX)是一种预测分子量为431kd的蛋白质,包含两个潜在的DNA结合基序,其中一个由与果蝇蛋白保守的锌指组成,另一个是与HMG蛋白中的DNA结合基序相关的非保守氨基末端“AT钩”基序。11q23易位在这两个基序之间破坏了HRX基因,在一个携带t(11;19)的细胞系中,两个衍生染色体均表达融合转录本。衍生的11号转录本更为丰富,其编码一种嵌合蛋白,该蛋白包含与19号染色体上一个先前未描述的蛋白(ENL)融合的AT钩基序。这些数据表明,三体胸蛋白同源蛋白在多谱系人类白血病中具有新的作用,可能是通过在富含AT的位点的小沟内进行DNA结合来介导的,这与细菌IHF、酵母datin和哺乳动物HMG介导的基因激活中发挥重要作用有关。