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首页> 外文期刊>Fish Physiology and Biochemistry >Organization and promoter analysis of the zebrafish (Danio rerio) chemokine gene (CXC-64) promoter
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Organization and promoter analysis of the zebrafish (Danio rerio) chemokine gene (CXC-64) promoter

机译:斑马鱼(Danio rerio)趋化因子基因(CXC-64)启动子的组织和启动子分析

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Zebrafish CXC-64, a chemokine representing a superfamily of chemotactic cytokines present in fish, is involved in recruitment, activation, and response to inflammatory stimulation. We cloned and sequenced the genomic DNA of the zebrafish CXC-64 chemokine; it was most similar to CXCL11 from humans and CXCL10 from a catfish. The zebrafish CXC-64 gene is approximately 4.0 kb long and has a four-exon, three-intron structure common to the human CXCL11 gene. However, the promoter region includes a typical TATA box and multi-transcription factor-binding sequences. To understand the roles of lipopolysaccharide (LPS), poly I:poly C, and tumor necrosis factor (TNF)-alpha in regulating zebrafish CXC-64 expression, serial deletions were made in the promoter region of this clone. Different fragments of the zebrafish CXC-64 5'-flanking region were transfected into RAW264.7 (mouse macrophage; Abelson murine leukemia virus transformed) and zfl (zebrafish liver) cells and then treated with 0, 10, 50, 100, and 200 ng/ml LPS, poly I:poly C, or TNF-alpha. The results showed that the promoter activity presented dose-dependent effects in LPS-treated RAW264.7 cells, TNF-alpha-treated RAW264.7 cells, and LPS-treated zfl cells. These results reveal that the zebrafish CXC-64 chemokine gene promoter region can be induced by LPS in both human and fish cell lines, which suggests that it plays an important role in regulating LPS.
机译:斑马鱼CXC-64是代表鱼中趋化性细胞因子超家族的趋化因子,它参与募集,激活和对炎症刺激的反应。我们克隆并测序了斑马鱼CXC-64趋化因子的基因组DNA。它与人类的CXCL11和a鱼的CXCL10最相似。斑马鱼CXC-64基因长约4.0 kb,具有人类CXCL11基因共有的四个外显子,三个内含子结构。然而,启动子区域包括典型的TATA盒和多转录因子结合序列。为了了解脂多糖(LPS),poly I:poly C和肿瘤坏死因子(TNF)-α在调节斑马鱼CXC-64表达中的作用,在该克隆的启动子区域进行了系列删除。将斑马鱼CXC-64 5'侧翼区域的不同片段转染到RAW264.7(小鼠巨噬细胞;转化的Abelson鼠白血病病毒)和zfl(斑马鱼肝脏)细胞中,然后分别用0、10、50、100和200处理ng / ml LPS,poly I:poly C或TNF-alpha。结果表明,启动子活性在LPS处理的RAW264.7细胞,TNF-α处理的RAW264.7细胞和LPS处理的zf1细胞中呈剂量依赖性。这些结果表明,LPS可在人和鱼细胞系中诱导斑马鱼CXC-64趋化因子基因启动子区域,这表明其在调节LPS中起重要作用。

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