Hüdepohl U, Reiter W D, Zillig W
Max-Planck-Institut für Biochemie, Munich, Federal Republic of Germany.
Proc Natl Acad Sci U S A. 1990 Aug;87(15):5851-5. doi: 10.1073/pnas.87.15.5851.
We describe a cell-free transcription system for the archaebacterium Sulfolobus sp. B12 that specifically initiates transcription at the 5S rRNA-encoding DNA and the 16S/23S rRNA-encoding DNA promoters of the same species. With this crude extract system, specific initiation was absolutely dependent on the box A motif, a highly conserved promoter element in archaebacteria located approximately 25 base pairs upstream of transcription initiation sites. In vitro transcription of the rRNA genes by purified RNA polymerase, however, resulted in semi-specific, box A-independent initiation, indicating that factor(s) in the crude extract were necessary for the highly specific box A-dependent transcription. Fractionation of the cell-free extract by sucrose-gradient centrifugation resulted in the identification of a low molecular weight fraction complementing purified RNA polymerase to an extract-like specificity.
我们描述了一种用于嗜热栖硫叶菌属物种B12的无细胞转录系统,该系统能特异性地在同一物种的5S rRNA编码DNA以及16S/23S rRNA编码DNA启动子处起始转录。在这个粗提物系统中,特异性起始绝对依赖于A框基序,这是古细菌中一种高度保守的启动子元件,位于转录起始位点上游约25个碱基对处。然而,用纯化的RNA聚合酶对rRNA基因进行体外转录,会导致半特异性的、不依赖A框的起始,这表明粗提物中的某种因子对于高度特异性的依赖A框的转录是必需的。通过蔗糖梯度离心对无细胞提取物进行分级分离,结果鉴定出一种低分子量级分,它能使纯化的RNA聚合酶具有类似提取物的特异性。