Barat C, Barbeau B, Delattre O, Rassart E
Département des Sciences Biologiques, Universite à Québec à Montréal, Canada.
Biochim Biophys Acta. 2000 Dec 15;1517(1):164-70. doi: 10.1016/s0167-4781(00)00239-6.
The mouse Fli-1 proto-oncogene is activated by proviral integration of four murine leukemia retroviruses and its human counterpart is translocated (11,22) in Ewing tumors. We have identified two alternative exons 1 by RACE analysis from a human neuroectodermal tumor. Exons 1a and 1b are located respectively 1.3 and 2.5 kb upstream from the published exon 1. Translation of these alternative messengers is predicted to generate very similar proteins. The sequence upstream from exon 1b showed functional promoter activity. Exon 1b was not conserved in the mouse but was detected in every analyzed human cell, whereas exon 1a was present only in a subset of them and also in various mouse cell lines. These results suggest that both mouse and human Fli-1 gene expression might be under the control of several independent promoter regions.
小鼠Fli-1原癌基因可被四种鼠白血病逆转录病毒的前病毒整合激活,其人类对应基因在尤因肿瘤中发生易位(11,22)。我们通过RACE分析从人类神经外胚层肿瘤中鉴定出两个选择性外显子1。外显子1a和1b分别位于已发表的外显子1上游1.3和2.5 kb处。预计这些选择性信使的翻译会产生非常相似的蛋白质。外显子1b上游的序列显示出功能性启动子活性。外显子1b在小鼠中不保守,但在每个分析的人类细胞中都能检测到,而外显子1a仅存在于其中一部分细胞以及各种小鼠细胞系中。这些结果表明,小鼠和人类Fli-1基因的表达可能受几个独立启动子区域的控制。