Bell S D, Jaxel C, Nadal M, Kosa P F, Jackson S P
Wellcome Trust/Cancer Research Campaign Institute of Cancer and Developmental Biology, and Department of Zoology Cambridge University, Tennis Court Road, Cambridge CB2 1QR United Kingdom.
Proc Natl Acad Sci U S A. 1998 Dec 22;95(26):15218-22. doi: 10.1073/pnas.95.26.15218.
Although Archaea are prokaryotic and resemble Bacteria morphologically, their transcription apparatus is remarkably similar to those of eukaryotic cell nuclei. Because some Archaea exist in environments with temperatures of around 100 degreesC, they are likely to have evolved unique strategies for transcriptional control. Here, we investigate the effects of temperature and DNA template topology in a thermophilic archaeal transcription system. Significantly, and in marked contrast with characterized eucaryal systems, archaeal DNA template topology has negligible effect on transcription levels at physiological temperatures using highly purified polymerase and recombinant transcription factors. Furthermore, archaeal transcription does not require hydrolysis of the beta-gamma phosphoanhydride bond of ATP. However, at lower temperatures, negatively supercoiled templates are transcribed more highly than those that are positively supercoiled. Notably, the block to transcription on positively supercoiled templates at lowered temperatures is at the level of polymerase binding and promoter opening. These data imply that Archaea do not possess a functional homologue of transcription factor TFIIH, and that for the promoters studied, transcription is mediated by TATA box-binding protein, transcription factor TFB, and RNA polymerase alone. Furthermore, they suggest that the reduction of plasmid linking number by hyperthermophilic Archaea in vivo in response to cold shock is a mechanism to maintain gene expression under these adverse circumstances.
虽然古生菌是原核生物,在形态上类似于细菌,但其转录装置与真核细胞核的转录装置非常相似。由于一些古生菌存在于温度约为100摄氏度的环境中,它们可能已经进化出独特的转录控制策略。在这里,我们研究了嗜热古生菌转录系统中温度和DNA模板拓扑结构的影响。值得注意的是,与已表征的真核生物系统形成鲜明对比的是,使用高度纯化的聚合酶和重组转录因子时,古生菌DNA模板拓扑结构在生理温度下对转录水平的影响可忽略不计。此外,古生菌转录不需要ATP的β-γ磷酸酐键水解。然而,在较低温度下,负超螺旋模板的转录比正超螺旋模板更高。值得注意的是,在较低温度下,正超螺旋模板上转录的阻滞发生在聚合酶结合和启动子开放水平。这些数据表明,古生菌不具有转录因子TFIIH的功能同源物,并且对于所研究的启动子,转录仅由TATA盒结合蛋白、转录因子TFB和RNA聚合酶介导。此外,它们表明嗜热古生菌在体内响应冷休克而降低质粒连接数是在这些不利条件下维持基因表达的一种机制。