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Cloning and characterisation of a nuclear site specific ssDNA binding protein.

机译:核和位点特异性ssDNA结合蛋白的克隆和鉴定。

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摘要

Estradiol inducible, liver-specific expression of the apoVLDL II gene is mediated through the estrogen receptor and a variety of other DNA-binding proteins. In the present study we report the cloning and characterisation of a single-strand DNA binding protein that interacts with the lower strand of a complex regulatory site, which includes the major estrogen responsive element and a site that resembles the rat albumin site D (apoVLDL II site D). Based on its binding specificity determined with electro-mobility shift assays, the protein is named single-strand D-box binding factor (ssDBF). Analysis of the deduced 302 amino acid sequence revealed that the protein belongs to the heteronuclear ribonucleoprotein A/B family (hnRNP A/B) and resembles other known eukaryotic single-strand DNA binding proteins. Transient transfection experiments in a chicken liver cell-line showed that the protein represses estrogen-induced transcription. A protein with similar binding characteristics is present in liver nuclear extract. The relevance of the occurrence of this protein to the expression of the apoVLDL II gene is discussed.
机译:雌二醇诱导的apoVLDL II基因的肝特异性表达是通过雌激素受体和多种其他DNA结合蛋白介导的。在本研究中,我们报告了与复杂调控位点下链相互作用的单链DNA结合蛋白的克隆和表征,该调控位点包括主要的雌激素反应元件和类似于大鼠白蛋白位点D(apoVLDL II网站D)。基于通过电动迁移分析测定的结合特异性,该蛋白质被称为单链D-box结合因子(ssDBF)。分析推导的302个氨基酸序列,发现该蛋白属于异核核糖蛋白A / B家族(hnRNP A / B),与其他已知的真核单链DNA结合蛋白相似。在鸡肝细胞系中进行的瞬时转染实验表明,该蛋白可抑制雌激素诱导的转录。具有相似结合特性的蛋白质存在于肝核提取物中。讨论了这种蛋白质的出现与apoVLDL II基因表达的相关性。

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