Suppr超能文献

含同源异型盒基因Evx-1对细胞趋触蛋白启动子的激活作用。

Activation of the cytotactin promoter by the homeobox-containing gene Evx-1.

作者信息

Jones F S, Chalepakis G, Gruss P, Edelman G M

机构信息

Laboratory of Developmental and Molecular Biology, Rockefeller University, New York, NY 10021.

出版信息

Proc Natl Acad Sci U S A. 1992 Mar 15;89(6):2091-5. doi: 10.1073/pnas.89.6.2091.

Abstract

Cytotactin is a morphoregulatory molecule of the extracellular matrix affecting cell shape, division, and migration that appears in a characteristic and complex site-restricted pattern during embryogenesis. The promoter region of the gene that encodes chicken cytotactin contains a variety of potential regulatory sequences. These include putative binding sites for homeodomain proteins and a phorbol 12-O-tetradecanoate 13-acetate response element (TRE)/AP-1 element, a potential target for transcription factors thought to be involved in growth-factor signal transduction. To determine the effects of homeobox-containing genes on cytotactin promoter activity, we conducted a series of cotransfection experiments on NIH 3T3 cells using cytotactin promoter-chloramphenicol acetyltransferase (CAT) reporter gene constructs and plasmids driving the expression of mouse homeobox genes Evx-1 and Hox-1.3. cotransfection with Evx-1 stimulated cytotactin promoter activity whereas cotransfection in control experiments with Hox-1.3 had no effect. To localize the sequences required for Evx-1 activation, we tested a series of deletions in the cytotactin promoter. An 89-base-pair region containing a consensus TRE/AP-1 element was found to be required for activation. An oligonucleotide segment containing this TRE/AP-1 site was found to confer Evx-1 inducibility on a simian virus 40 minimal promoter; mutation of the TRE/AP-1 site abolished this activity. To explore the potential role of growth factors in cytotactin promoter activation, chicken embryo fibroblasts, which are known to synthesize cytotactin, were first transfected with cytotactin promoter constructs and cultured under minimal conditions in 1% fetal bovine serum. Although the cells exhibited only low levels of CAT activity under these conditions, cells exposed for 12 h to 10% (vol/vol) fetal bovine serum showed a marked increase in CAT activity. Cotransfection with Evx-1 and cytotactin promoter constructs of cells cultured in 1% fetal bovine serum was sufficient, however, to produce high levels of CAT activity. These findings are consistent with the hypothesis that Evx-1, a homeobox-containing gene, may activate the cytotactin promoter by a mechanism involving a growth-factor signal transduction pathway. More generally, the results support the hypothesis that the place-dependent expression of morphoregulatory molecules may depend upon local cues provided by homeobox genes and their encoded proteins.

摘要

细胞趋触蛋白是一种细胞外基质的形态调节分子,影响细胞形状、分裂和迁移,在胚胎发育过程中以特征性且复杂的位点受限模式出现。编码鸡细胞趋触蛋白的基因启动子区域包含多种潜在调控序列。这些序列包括同源结构域蛋白的假定结合位点以及佛波酯12 - O - 十四烷酰佛波醇13 - 乙酸酯反应元件(TRE)/AP - 1元件,这是一个被认为参与生长因子信号转导的转录因子的潜在靶点。为了确定含同源框基因对细胞趋触蛋白启动子活性的影响,我们使用细胞趋触蛋白启动子 - 氯霉素乙酰转移酶(CAT)报告基因构建体和驱动小鼠同源框基因Evx - 1和Hox - 1.3表达的质粒,对NIH 3T3细胞进行了一系列共转染实验。与Evx - 1共转染刺激了细胞趋触蛋白启动子活性,而在对照实验中与Hox - 1.3共转染则没有影响。为了定位Evx - 1激活所需的序列,我们测试了细胞趋触蛋白启动子中的一系列缺失。发现一个包含共有TRE/AP - 1元件的89个碱基对区域是激活所必需的。发现一个包含该TRE/AP - 1位点的寡核苷酸片段可赋予猿猴病毒40最小启动子Evx - 1诱导性;TRE/AP - 1位点的突变消除了这种活性。为了探索生长因子在细胞趋触蛋白启动子激活中的潜在作用,已知能合成细胞趋触蛋白的鸡胚成纤维细胞首先用细胞趋触蛋白启动子构建体进行转染,并在1%胎牛血清的最小条件下培养。尽管在这些条件下细胞仅表现出低水平的CAT活性,但暴露于10%(体积/体积)胎牛血清12小时的细胞显示出CAT活性显著增加。然而,在1%胎牛血清中培养的细胞与Evx - 1和细胞趋触蛋白启动子构建体共转染足以产生高水平的CAT活性。这些发现与以下假设一致,即含同源框基因Evx - 1可能通过涉及生长因子信号转导途径的机制激活细胞趋触蛋白启动子。更普遍地说,这些结果支持了形态调节分子的位置依赖性表达可能取决于同源框基因及其编码蛋白提供的局部线索这一假设。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5835/48602/faeab807e0aa/pnas01080-0104-a.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验