Schmidt M C, Chamberlin M J
Department of Biochemistry, University of California, Berkeley 94720.
J Mol Biol. 1987 Jun 20;195(4):809-18. doi: 10.1016/0022-2836(87)90486-4.
We have studied the factors that affect transcription termination in vitro at the tR2 terminator of bacteriophage lambda and at the T1 terminator of the Escherichia coli rrnB operon. Termination efficiency at both of these sites is enhanced by the E. coli nusA protein, giving final efficiencies of termination in vitro comparable to those estimated in vivo. Transcripts terminated in the presence of nusA protein are all released from the RNA polymerase complex, indicating that a complete termination reaction is involved, rather than simply induction of a long pause at the terminator. The termination factor activity of the nusA protein does not depend on the presence of rho protein and is not detectably enhanced by that factor. Thus, the nusA protein appears to play a pleiotropic role in E. coli transcription, serving as an antitermination factor, RNA polymerase subunit and true termination factor for some terminator sites.
我们研究了影响噬菌体λ的tR2终止子以及大肠杆菌rrnB操纵子的T1终止子体外转录终止的因素。大肠杆菌nusA蛋白可提高这两个位点的终止效率,使体外终止的最终效率与体内估计值相当。在nusA蛋白存在下终止的转录本均从RNA聚合酶复合物中释放出来,这表明涉及完整的终止反应,而不仅仅是在终止子处诱导长时间停顿。nusA蛋白的终止因子活性不依赖于rho蛋白的存在,且该因子也未显著增强其活性。因此,nusA蛋白似乎在大肠杆菌转录中发挥多效性作用,作为某些终止子位点的抗终止因子、RNA聚合酶亚基和真正的终止因子。