Lopingco M C, Perkins A S
Department of Pathology, Yale University School of Medicine, New Haven, CT 06520-8023, USA.
Curr Top Microbiol Immunol. 1996;211:211-22. doi: 10.1007/978-3-642-85232-9_21.
Through chromosomal rearrangements and/or proviral insertions, a number of genes encoding nuclear transcription factors have been identified that play key roles in leukemogenesis. One of these is Evi1, which plays a role in both murine and human myeloid leukemia. The exact mechanism by which Evi1 exerts its leukemogenic effect is not clear, but it may involve the inhibition of terminal differentiation, through the abnormal repression of genes necessary for cellular maturation. Our analysis of the DNA binding characteristics of EVI1 indicate a high degree of specificity, which likely indicates that the protein acts on a tightly defined number of targets in the cell. We are beginning to characterize candidate target genes located in the mouse genome near EVI1 binding sites with the expectation that these will yield insight into EVI1 function both in normal cells and in leukemogenesis.
通过染色体重排和/或前病毒插入,已鉴定出一些编码核转录因子的基因,它们在白血病发生过程中起关键作用。其中之一是Evi1,它在小鼠和人类髓系白血病中均发挥作用。Evi1发挥其致白血病作用的确切机制尚不清楚,但可能涉及通过异常抑制细胞成熟所需基因来抑制终末分化。我们对EVI1的DNA结合特性分析表明其具有高度特异性,这可能表明该蛋白作用于细胞中数量有限的特定靶标。我们开始对位于小鼠基因组中靠近EVI1结合位点的候选靶基因进行表征,期望这些研究能够深入了解EVI1在正常细胞和白血病发生过程中的功能。