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首页> 外文期刊>Biogerontology >Characterization of a novel positive transcription regulatory element that differentially regulates the alpha-2-macroglobulin gene in replicative senescence
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Characterization of a novel positive transcription regulatory element that differentially regulates the alpha-2-macroglobulin gene in replicative senescence

机译:新型正转录调控元件的特征,该元件在复制性衰老中差异性地调控α-2-巨球蛋白基因

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摘要

Alpha-2-macroglobulin (α2M), a protease inhibitor, is implicated in Alzheimer's disease, atherosclerosis, and other age-related diseases. The elevated level of α2M mRNA has been described in replicative senescence and it could be used as a biomarker of the aging cells. However, the mechanism responsible for the up-regulation of its expression is still unclear. This report identified a novel transcriptional regulatory element, the α2M transcription enhancement element (ATEE), within the α2M promoter. This element differentially activates α2M expression in senescent versus young fibroblasts. Electrophoretic mobility shift assays revealed abundant complexes in senescent cell nuclear extracts compared with young cell nuclear extracts. The DNase I footprint revealed the protein-binding core sequence through which the protein binds the ATEE. Mutation within ATEE selectively abolished α2M promoter activity in senescent (but not young) cells. These results indicated the ATEE, as a positive transcription regulatory element, contributes to the up-regulation of α2M during replicative senescence.
机译:蛋白酶抑制剂α-2-巨球蛋白(α2M)与阿尔茨海默氏病,动脉粥样硬化和其他与年龄有关的疾病有关。已经在复制衰老中描述了升高的α2MmRNA水平,其可以用作衰老细胞的生物标记。但是,尚不清楚其表达上调的机制。该报告鉴定了α2M启动子中的新型转录调控元件,即α2M转录增强元件(ATEE)。与衰老的成纤维细胞相比,该元素差异性地激活了α2M的表达。电泳迁移率变化分析显示,与年轻细胞核提取物相比,衰老细胞核提取物中有大量复合物。 DNase I足迹揭示了蛋白质结合核心序列,蛋白质通过该核心序列结合ATEE。 ATEE中的突变选择性地消除了衰老(但不是年轻)细胞中的α2M启动子活性。这些结果表明,作为正转录调节元件的ATEE在复制衰老过程中促进了α2M的上调。

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