Takahashi N, Hotta H, Homma M
Department of Microbiology, Kobe University School of Medicine.
Jpn J Cancer Res. 1991 Nov;82(11):1239-44. doi: 10.1111/j.1349-7006.1991.tb01787.x.
A deletion mutant of the human melanoma-associated ME491 antigen gene starting at the first intron (lambda R31) differentially mediates the antigen expression depending on the cell type. Cryptic promoter activity residing in a 270-base-pair (bp) fragment of the first intron was examined by primer extension analysis and recombinant chloramphenicol acetyltransferase (CAT) assay. The cryptic promoter, further localized within a 153-bp fragment (fr153BN), exerted its effect in Ltk- and H-ras-transformed NIH3T3 (3T3-Hras) but not in parental NIH3T3 cells. The results suggested that the cryptic promoter was associated with a novel ras-responsive positive regulatory element, since fr153BN did not contain an AP-1-binding sequence motif, known as the ras-responsive enhancer element. The cryptic promoter activity of fr153BN was suppressed by an upstream 121-bp fragment (fr121SB) which contained a consensus sequence motif for binding of a repressor protein, GC factor, and regions showing sequence similarity with putative cis-acting repressor elements found in the vimentin gene. The degree of the suppression was greater in 3T3-Hras than in Ltk- cells. These positive and negative regulatory elements may be differentially involved in the regulation of ME491 antigen expression depending on the cell type.
一种从第一个内含子开始的人黑素瘤相关ME491抗原基因的缺失突变体(λR31),其介导抗原表达的方式因细胞类型而异。通过引物延伸分析和重组氯霉素乙酰转移酶(CAT)测定法,检测了位于第一个内含子270个碱基对(bp)片段中的隐蔽启动子活性。进一步定位于153 bp片段(fr153BN)内的隐蔽启动子,在Ltk -和H - ras转化的NIH3T3(3T3 - Hras)细胞中发挥作用,但在亲本NIH3T3细胞中则不然。结果表明,该隐蔽启动子与一种新的ras反应性正调控元件相关,因为fr153BN不包含已知的ras反应性增强子元件AP - 1结合序列基序。fr153BN的隐蔽启动子活性被上游121 bp片段(fr121SB)抑制,该片段包含阻遏蛋白GC因子结合的共有序列基序,以及与波形蛋白基因中推定的顺式作用阻遏元件具有序列相似性的区域。3T3 - Hras细胞中的抑制程度大于Ltk -细胞。这些正调控和负调控元件可能因细胞类型而异,参与ME491抗原表达的调控。