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Transcription initiation from TATA-less promoters within eukaryotic protein-coding genes

机译:真核蛋白质编码基因中无TATA的启动子的转录起始

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摘要

Since 1979, when cell-free extracts that support accurate transcription by RNA polymerase II were first reported 1 , the basic biochemical mechanisms of transcription initiation from protein-coding genes have been dissected in considerable detail 2–4. Numerous laboratories have contributed to this analysis, with virtually all of the key advances involving studies of promoters whose activities depend on a common control element known as a TATA box 5–9 . In metazoan genes, the TATA box is located 25–30 bp upstream of the transcription start site and directs accurate transcription initiation through a mechanism that depends on its specific interaction with a protein called TBP TATA-binding protein 10–14.
机译:自1979年以来,首次报道了支持RNA聚合酶II准确转录的无细胞提取物1,从蛋白质编码基因开始转录的基本生化机制已被详细剖析2-4。许多实验室都为这种分析做出了贡献,几乎所有关键进展都涉及启动子的研究,这些启动子的活性取决于一个称为TATA框5-9的共同控制元件。在后生动物基因中,TATA盒位于转录起始位点上游25–30 bp,并通过一种机制指导准确的转录起始,该机制取决于它与一种称为TBP TATA结合蛋白10–14的蛋白质的特异性相互作用。

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