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首页> 外文期刊>Nucleic acids research >The binding site for the liver-specific transcription factor Tf-LF1 and the TATA box of the human transferrin gene promoter are the only elements necessary to direct liver-specific transcription in vitro
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The binding site for the liver-specific transcription factor Tf-LF1 and the TATA box of the human transferrin gene promoter are the only elements necessary to direct liver-specific transcription in vitro

机译:肝脏特异性转录因子Tf-LF1的结合位点和人转铁蛋白基因启动子的TATA框是在体外指导肝脏特异性转录的唯一要素

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摘要

We have studied the liver-specific transcriptional activity of the human transferrin gene promoter. Results of competition experiments, site-directed mutagenesis, and 5′ deletion analysis have demonstrated that a TATA box and a binding site for the liver-specific protein Tf-LF1 are the only elements needed to direct hepatic-specific transcription in vitro. Thus, Tf-LF1 behaves as other previously described proteins, HNF-1, DBP and LF-A1, in that it Is sufficient to confer liver-specific transcriptional activity to a promoter in vitro. This results contrast with observations made in transient expression experiments, in which Tf-LF1 binding alone cannot direct hepatic-specific expression, and the binding of at least one more protein, similar to C/EBP, Is needed. Thus, as described for other hepatic genes, the number of elements necessary to confer tissue specificity is different in vivo and in vitro.
机译:我们已经研究了人类转铁蛋白基因启动子的肝脏特异性转录活性。竞争实验,定点诱变和5'缺失分析的结果表明,TATA盒和肝脏特异性蛋白Tf-LF1的结合位点是体外指导肝特异性转录的唯一要素。因此,Tf-LF1的行为与其他先前描述的蛋白HNF-1,DBP和LF-A1相同,因为它足以在体外将肝特异性转录活性赋予启动子。该结果与瞬时表达实验中的观察结果相反,在瞬时表达实验中,单独的Tf-LF1结合不能指导肝特异性表达,并且需要至少一种与C / EBP类似的蛋白质结合。因此,如针对其他肝基因所述,赋予组织特异性所必需的元件数目在体内和体外是不同的。

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