Copertino D W, Jenkinson S, Jones F S, Edelman G M
Scripps Research Institute, Department of Neurobiology, La Jolla, CA 92037.
Proc Natl Acad Sci U S A. 1995 Mar 14;92(6):2131-5. doi: 10.1073/pnas.92.6.2131.
Cytotactin/tenascin is an extracellular matrix glycoprotein expressed in a restricted anteroposterior pattern during vertebrate development and is reexpressed in the adult during wound healing, tumorigenesis, and nerve regeneration. Previously, we have characterized the chicken cytotactin promoter and have shown its regulation by homeobox gene products in vitro. We have now isolated the promoter for the mouse tenascin gene in order to determine whether common or different DNA regulatory elements control the expression of this gene in these two species. Like the chicken cytotactin gene, the mouse tenascin gene has a single RNA start site that lies 27 bp downstream of a TATA box. A 4028-bp region of DNA upstream of the mouse tenascin gene was sequenced and examined for regulatory motifs in common with the upstream sequence from the chicken cytotactin promoter. Two hundred thirty base pairs of the proximal promoter regions from both genes had an extended sequence similarity and contained common regulatory motifs such as two tracts of homopolymeric dA.dT sequence, an octamer motif, an ATTA (TAAT) motif which is a common core sequence for binding of homeodomain transcription factors, and a TATA-box/cap-site region. Reporter gene constructs with various 5' deletions of the mouse tenascin upstream sequence were tested in transient transfections of mouse NIH 3T3 and chicken embryo fibroblasts. The conserved proximal promoter region of tenascin was responsible for most of the positive regulatory activity. In addition, an upstream region (-2478 to -247) repressed proximal promoter activity in mouse fibroblasts and also in chicken embryo fibroblasts. These data indicate that both the structure and function of the cytotactin/tenascin proximal promoters have remained conserved over 250 million years.
细胞趋触蛋白/腱生蛋白是一种细胞外基质糖蛋白,在脊椎动物发育过程中以前后受限的模式表达,在成体的伤口愈合、肿瘤发生和神经再生过程中重新表达。以前,我们已对鸡细胞趋触蛋白启动子进行了特性分析,并在体外显示了其受同源框基因产物的调控。我们现在分离出了小鼠腱生蛋白基因的启动子,以确定是共同的还是不同的DNA调控元件控制这两个物种中该基因的表达。与鸡细胞趋触蛋白基因一样,小鼠腱生蛋白基因有一个单一的RNA起始位点,位于TATA框下游27 bp处。对小鼠腱生蛋白基因上游4028 bp的DNA区域进行了测序,并检查了与鸡细胞趋触蛋白启动子上游序列共有的调控基序。两个基因的近端启动子区域的230个碱基对有扩展的序列相似性,并包含共同的调控基序,如两段同聚dA.dT序列、一个八聚体基序、一个ATTA(TAAT)基序(这是同源结构域转录因子结合的常见核心序列)以及一个TATA框/帽位点区域。用小鼠腱生蛋白上游序列的各种5'缺失构建的报告基因构建体在小鼠NIH 3T3和鸡胚成纤维细胞的瞬时转染中进行了测试。腱生蛋白保守的近端启动子区域负责大部分的正调控活性。此外,一个上游区域(-2478至-247)在小鼠成纤维细胞和鸡胚成纤维细胞中均抑制近端启动子活性。这些数据表明,细胞趋触蛋白/腱生蛋白近端启动子的结构和功能在超过2.5亿年的时间里一直保持保守。