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Comparative sequence analysis of the mouse and human transferrin promoters: hormonal regulation of the transferring promoter in Sertoli cells.

机译:小鼠和人类运铁蛋白启动子的比较序列分析:Sertoli细胞中转移启动子的激素调节。

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摘要

A 3-kb mouse transferrin promoter was cloned and sequenced. Comparison with the human transferrin promoter revealed a conserved regulatory element; the proximal 90 bp of the promoter was 80% homologous in the 2 species. The previously identified protected regions in the proximal human promoter were also conserved in the mouse transferrin promoter. Sequence analysis revealed that an E-box response element was also conserved between mouse and human promoters. Deletion mutants of the mouse transferrinpromoter were generated in chloramphenicol acetyl transferase reporter constructs to study the regulation of the transferrin promoter in Sertoli cells. The mouse 581-bp proximal transferrin promoter was sufficient to obtain basal expression. A putativec-AMP response element in the minimal promoter may be needed for FSH actions mediated via c-AMP. Other regulatory agents, such as the testicular paracrine factor PModS, used elements in the upstream region. A repressor was identified 2.5 kb upstream fromthe start site of translation. It is suggested that a minimal promoter is sufficient for basal transcription, but the upstream regions of the promoter are needed for the hormonal regulation of the transferrin gene in Sertoli cells.
机译:克隆3-kb小鼠转铁蛋白启动子并测序。与人运铁蛋白启动子的比较揭示了保守的调节元件;在两个物种中,启动子的近端90 bp是80%同源的。在近端人类启动子中先前鉴定的保护区在小鼠运铁蛋白启动子中也保守。序列分析表明,E-box反应元件在小鼠和人类启动子之间也保守。在氯霉素乙酰基转移酶报告基因构建物中产生了小鼠转铁蛋白启动子的缺失突变体,以研究Sertoli细胞中转铁蛋白启动子的调控。小鼠581-bp近端转铁蛋白启动子足以获得基础表达。通过c-AMP介导的FSH作用可能需要最小启动子中的推定c-AMP反应元件。其他调节剂,例如睾丸旁分泌因子PModS,在上游区域使用了元素。在翻译起始位点上游2.5 kb处鉴定到阻遏物。提示最小的启动子足以进行基础转录,但是启动子的上游区域对于Sertoli细胞中转铁蛋白基因的激素调节是必需的。

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