Morishita K, Parganas E, Douglass E C, Ihle J N
Department of Biochemistry, St. Jude Children's Research Hospital, Memphis, Tennessee 38105.
Oncogene. 1990 Jul;5(7):963-71.
Retroviral insertional activation of the expression of the Evi-1 is one of the most common events associated with transformation in murine myeloid leukemia. The murine Evi-1 gene encodes a 145 kDa nuclear, DNA binding protein that contains two domains containing seven and three sets of repeats of the zinc finger motif. During studies to determine the role of the Evi-1 gene in the transformation of human cells, we have found that the Evi-1 gene is uniquely expressed at low levels in HEC-1-A cells and at high levels in HEC-1-B cells, two related human endometrial carcinoma cell lines. cDNA clones were isolated and sequenced from the HEC-1-B cell line. The human gene is highly homologous to the murine gene and shows 91% and 94% homology in nucleotide or amino acid sequence respectively. In addition an alternatively spliced form of the gene was identified that encodes a protein with an internal deletion 315 amino acids including two of the zinc finger repeats. The possible basis for the unique expression of the Evi-1 gene by HEC-1 cells could not be determined by karyotype or Southern blot analysis.
逆转录病毒插入激活Evi-1的表达是小鼠髓系白血病转化相关的最常见事件之一。小鼠Evi-1基因编码一种145 kDa的核DNA结合蛋白,该蛋白包含两个结构域,分别含有七组和三组锌指基序重复序列。在确定Evi-1基因在人类细胞转化中的作用的研究过程中,我们发现Evi-1基因在两种相关的人子宫内膜癌细胞系HEC-1-A细胞中低水平独特表达,而在HEC-1-B细胞中高水平表达。从HEC-1-B细胞系中分离并测序了cDNA克隆。人类基因与小鼠基因高度同源,核苷酸序列和氨基酸序列的同源性分别为91%和94%。此外,还鉴定出该基因的一种选择性剪接形式,其编码的蛋白质有一个315个氨基酸的内部缺失,包括两个锌指重复序列。通过核型分析或Southern印迹分析无法确定HEC-1细胞独特表达Evi-1基因的可能原因。