Rao Manjeet K, Maiti Sourindra, Ananthaswamy Honnavara N, Wilkinson Miles F
Department of Immunology, the University of Texas M. D. Anderson Cancer Center, Houston, Texas 77030, USA.
J Biol Chem. 2002 Jul 19;277(29):26036-45. doi: 10.1074/jbc.M203374200. Epub 2002 May 1.
One mechanism by which normal cells become converted to tumor cells involves the aberrant transcriptional activation of genes that are normally silent. We characterize a promoter that normally exhibits highly tissue- and stage-specific expression but displays ubiquitous expression when cells become immortalized or malignant, regardless of their lineage or tissue origin. This promoter normally drives the expression of the Pem homeobox gene in specific cell types in ovary and placenta but is aberrantly expressed in lymphomas, neuroblastomas, retinoblastomas, carcinomas, and sarcomas. By deletion analysis we identified a region between nucleotides -80 and -104 that was absolutely critical for the expression from this distal Pem promoter (Pem Pd). Site-specific mutagenesis and transfection studies revealed that this region contains two consensus Ets sites and a single Sp1 site that were necessary for Pem Pd expression. Gel shift analysis showed that Ets and Sp1 family members bound to these sites. Transfection studies demonstrated that the Ets family members Elf1 and Gabp and the Sp1 family members Sp1 and Sp3 transactivated the Pem Pd. Surprisingly, we found that Sp3 was a more potent activator of the Pem Pd than was Sp1; this is unusual, because Sp3 is either a weak activator or a repressor of most other promoters. Activation by either Elf1 or Gabp required an intact Sp1 family member binding site, suggesting that Ets and Sp1 family members cooperate to activate Pem Pd transcription. Expression from the Pem Pd (either transiently transfected or endogenous) depended on the Ras pathway, which could explain both its Ets- and Sp1-dependent expression in normal cells and its aberrant expression in tumor cells, in which ras protooncogenes are frequently mutated. We suggest that the Pem Pd may be a useful model system to understand the molecular mechanism by which a tissue-specific promoter can be corrupted in tumor cells.
正常细胞转变为肿瘤细胞的一种机制涉及通常沉默的基因发生异常转录激活。我们鉴定了一个启动子,它通常表现出高度的组织和阶段特异性表达,但当细胞永生化或发生恶性转化时,无论其谱系或组织来源如何,都会呈现普遍表达。该启动子通常在卵巢和胎盘中的特定细胞类型中驱动Pem同源框基因的表达,但在淋巴瘤、神经母细胞瘤、视网膜母细胞瘤、癌和肉瘤中异常表达。通过缺失分析,我们确定了核苷酸 -80 至 -104 之间的一个区域,该区域对于该远端Pem启动子(Pem Pd)的表达绝对至关重要。位点特异性诱变和转染研究表明,该区域包含两个共有Ets位点和一个单一的Sp1位点,这些位点对于Pem Pd表达是必需的。凝胶迁移分析表明Ets和Sp1家族成员与这些位点结合。转染研究证明Ets家族成员Elf1和Gabp以及Sp1家族成员Sp1和Sp3可反式激活Pem Pd。令人惊讶的是,我们发现Sp3是比Sp1更有效的Pem Pd激活剂;这很不寻常,因为Sp3对于大多数其他启动子要么是弱激活剂,要么是抑制剂。Elf1或Gabp的激活需要完整的Sp1家族成员结合位点,这表明Ets和Sp1家族成员协同激活Pem Pd转录。Pem Pd的表达(无论是瞬时转染的还是内源性的)依赖于Ras途径,这可以解释其在正常细胞中的Ets和Sp1依赖性表达以及在肿瘤细胞中的异常表达,在肿瘤细胞中ras原癌基因经常发生突变。我们认为Pem Pd可能是一个有用的模型系统,用于理解组织特异性启动子在肿瘤细胞中被破坏的分子机制。