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CLONING AND FUNCTIONAL ANALYSIS OF THE TATA BINDING PROTEIN FROM SULFOLOBUS SHIBATAE

机译:柴胡烟草中塔塔结合蛋白的克隆及功能分析

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摘要

Archaea (formerly archaebacteria) comprise a domain of life that is phylogenetically distinct from both Eucarya and Bacteria. Here we report the cloning of a gene from the Archaeon Sulfolobus shibatae that encodes a protein with strong homology to the TATA binding protein (TBP) of eukaryotes. Sulfolobus shibatae TBP is, however, almost as diverged from other archaeal TBPs that have been cloned as it is from eukaryotic TBPs. DNA binding studies indicate that S.shibatae TBP recognizes TATA-like A-box sequences that are present upstream of most archaeal genes. By quantitatively immunodepleting S.shibatae TBP from an in vitro transcription system, we demonstrate that Sulfolobus RNA polymerase is capable of transcribing the 16S/23S rRNA promoter weakly in the absence of TBP. Most significantly, we show that addition of recombinant S.shibatae TBP to this immunodepleted system leads to transcriptional stimulation and that this stimulation is dependent on the A-box sequence of the promoter. Taken together, these findings reveal fundamental similarities between the transcription machineries of Archaea and eukaryotes.
机译:古细菌(以前的古细菌)构成了一个生命域,在系统发育上不同于真车亚目和细菌。在这里,我们报道了从古细菌古细菌Shibatae的一个基因克隆,该基因编码一种与真核生物的TATA结合蛋白(TBP)具有高度同源性的蛋白。但是,Shibatae的Sulfolobus TBP与从真核TBP中克隆的其他古细菌TBP几乎一样。 DNA结合研究表明,shibatae TBP可识别大多数古细菌基因上游存在的TATA样A-box序列。通过从体外转录系统定量免疫消减志贺氏菌TBP,我们证明了在没有TBP的情况下,Sulfolobus RNA聚合酶能够弱转录16S / 23S rRNA启动子。最重要的是,我们表明向该免疫耗尽系统中添加重组志贺杆菌TBP会导致转录刺激,并且这种刺激取决于启动子的A-box序列。综上所述,这些发现揭示了古细菌和真核生物的转录机制之间的基本相似性。

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