Ohno T, Rao V N, Reddy E S
Department of Microbiology and Immunology, Jefferson Cancer Institute, Philadelphia, Pennsylvania 19107-5541.
Cancer Res. 1993 Dec 15;53(24):5859-63.
Fli-1, an ets related gene, was found to be rearranged in 75% of erythroleukemias induced by Friend murine leukemia virus. We have shown previously that the Fli-1 gene codes for a sequence specific transcriptional activator which contains two autonomous transcriptional activation domains, one at the amino terminal region and the other at the carboxy terminal region. Recently human Fli-1 gene was shown to be involved in Ewing's sarcoma and related subtypes of primitive neuroectodermal tumors which share t(11;22) (q24;q12) chromosome translocation. In these tumors the carboxyl terminal region of Fli-1 was found to be fused with the amino terminal region of a putative RNA binding protein, EWS. Because part of the amino terminal transcriptional activation domain of Fli-1 was replaced with the amino terminal domain of the EWS (NTD-EWS) which shares homology with RNA polymerase II, it was speculated that NTD-EWS may interfere with RNA pol II function. Alternatively, NTD-EWS could also contribute to the transcriptional activation function of EWS/Fli-1 chimeric protein by providing either a modulatory/regulatory domain or a novel transcriptional activation domain. Here we show that EWS/Fli-1 chimeric protein functions as a transcriptional activator. Deletion analysis reveals that the EWS domain functions as a modulatory/regulatory domain for the transcriptional activation properties of the carboxy terminal transcriptional activation domain of EWS/Fli-1. We therefore propose that replacement of the amino terminal transcriptional activation domain of the Fli-1 protein with the regulatory domain of NTD-EWS results in the activation of the carboxy terminal transcriptional activation domain of Fli-1 which may be the molecular mechanism involved in these human tumors.
Fli-1是一种与ets相关的基因,在Friend小鼠白血病病毒诱导的75%的红白血病中发现其发生了重排。我们之前已经表明,Fli-1基因编码一种序列特异性转录激活因子,该因子包含两个自主转录激活结构域,一个位于氨基末端区域,另一个位于羧基末端区域。最近发现人类Fli-1基因与尤因肉瘤及原始神经外胚层肿瘤的相关亚型有关,这些肿瘤都存在t(11;22)(q24;q12)染色体易位。在这些肿瘤中,发现Fli-1的羧基末端区域与一种假定的RNA结合蛋白EWS的氨基末端区域融合。由于Fli-1的部分氨基末端转录激活结构域被与RNA聚合酶II具有同源性的EWS的氨基末端结构域(NTD-EWS)所取代,推测NTD-EWS可能会干扰RNA聚合酶II的功能。或者,NTD-EWS也可能通过提供一个调节/调控结构域或一个新的转录激活结构域来促进EWS/Fli-1嵌合蛋白的转录激活功能。在这里我们表明EWS/Fli-1嵌合蛋白起到转录激活因子的作用。缺失分析表明,EWS结构域对EWS/Fli-1羧基末端转录激活结构域的转录激活特性起到调节/调控结构域的作用。因此我们提出,用NTD-EWS的调节结构域取代Fli-1蛋白的氨基末端转录激活结构域会导致Fli-1羧基末端转录激活结构域的激活,这可能是这些人类肿瘤所涉及的分子机制。