De Plaen E, Naerhuyzen B, De Smet C, Szikora J P, Boon T
Ludwig Institute for Cancer Research, Brussels Branch, Belgium.
Genomics. 1997 Mar 1;40(2):305-13. doi: 10.1006/geno.1996.4566.
Gene MAGE-4 (HGMW-approved symbol MAGE4) is expressed in several types of tumors, but not in normal tissues, except testis and placenta. The 5' end of this gene contains eight homologous exons spread over a 5.8-kb region. These exons are alternatively spliced to a unique second exon and a unique third exon, which encodes a protein of 317 amino acids. The analysis of transcripts found in testis, placenta, and a sarcoma cell line showed that each of the alternative first exons is used in at least one of these tissues. Various regions of the promoter of the fifth alternative exon (1.5) were cloned in a luciferase reporter plasmid, and the constructs were transfected in a sarcoma cell line that expresses MAGE-4. Two Ets motifs located between positions -70 and -29 relative to the transcription start site were found to drive 55% of the promoter activity. A region containing a Sp1 consensus binding site located upstream of the two Ets motifs was found to be responsible for 44% of the transcriptional activity. MAGE-4a promoters 1.4 and 1.6, which also contain the Sp1 and the two Ets binding motifs, supported a level of transcription comparable to that of promoter 1.5, whereas promoter 1.1, which contains only one Ets binding site, was sixfold less active. In line with observations made with gene MAGE-1 (HGMW-approved symbol MAGE1), we found that promoter 1.5 stimulated a high level of transcription in a melanoma cell line that does not express MAGE-4. This suggests that the tumor-specific expression of MAGE genes is not determined by the presence of specific transcription factors.
基因MAGE-4(HGMW批准的符号为MAGE4)在多种肿瘤类型中表达,但在正常组织中不表达,睾丸和胎盘除外。该基因的5'端包含八个同源外显子,分布在5.8kb的区域。这些外显子可选择性剪接至一个独特的第二个外显子和一个独特的第三个外显子,后者编码一个317个氨基酸的蛋白质。对睾丸、胎盘和一个肉瘤细胞系中发现的转录本分析表明,每个选择性的第一个外显子至少在这些组织中的一种中被使用。第五个选择性外显子(1.5)启动子的各个区域被克隆到荧光素酶报告质粒中,并将构建体转染到表达MAGE-4的肉瘤细胞系中。相对于转录起始位点,在-70至-29位置之间发现的两个Ets基序可驱动55%的启动子活性。发现在两个Ets基序上游包含一个Sp1共有结合位点的区域负责44%的转录活性。同样包含Sp1和两个Ets结合基序的MAGE-4a启动子1.4和1.6支持的转录水平与启动子1.5相当,而仅包含一个Ets结合位点的启动子1.1活性则低六倍。与对基因MAGE-1(HGMW批准的符号为MAGE1)的观察结果一致,我们发现启动子1.5在不表达MAGE-4的黑色素瘤细胞系中刺激了高水平的转录。这表明MAGE基因的肿瘤特异性表达不是由特定转录因子的存在所决定的。