Hausner W, Thomm M
Institut für Allgemeine Mikrobiologie, Christian-Albrechts-Universität zu Kiel, Am Botanischen Garten 1-9, D-24118 Kiel, Federal Republic of Germany.
J Bacteriol. 2001 May;183(10):3025-31. doi: 10.1128/JB.183.10.3025-3031.2001.
Transcription in Archaea is initiated by association of a TATA box binding protein (TBP) with a TATA box. This interaction is stabilized by the binding of the transcription factor IIB (TFIIB) orthologue TFB. We show here that the RNA polymerase of the archaeon Methanococcus, in contrast to polymerase II, does not require hydrolysis of the beta-gamma bond of ATP for initiation of transcription and open complex formation on linearized DNA. Permanganate probing revealed that the archaeal open complex spanned at least the DNA region from -11 to -1 at a tRNA(Val) promoter. The Methanococcus TBP-TFB promoter complex protected the DNA region from -40 to -14 on the noncoding DNA strand and the DNA segment from -36 to -17 on the coding DNA strand from DNase I digestion. This DNase I footprint was extended only to the downstream end by the addition of the RNA polymerase to position +17 on the noncoding strand and to position +13 on the coding DNA strand.
古菌中的转录起始是由TATA框结合蛋白(TBP)与TATA框结合引发的。转录因子IIB(TFIIB)的直系同源物TFB的结合可稳定这种相互作用。我们在此表明,与聚合酶II不同,古菌甲烷球菌的RNA聚合酶在以线性化DNA起始转录和形成开放复合物时,不需要ATP的β-γ键水解。高锰酸盐探测显示,在tRNA(Val)启动子处,古菌开放复合物至少跨越了从-11到-1的DNA区域。甲烷球菌TBP-TFB启动子复合物保护非编码DNA链上从-40到-14的DNA区域以及编码DNA链上从-36到-17的DNA片段不被DNase I消化。通过添加RNA聚合酶,使非编码链上的位置达到+17,编码DNA链上的位置达到+13,这种DNase I足迹仅向下游末端延伸。