Greenblatt J, Li J
Cell. 1981 May;24(2):421-8. doi: 10.1016/0092-8674(81)90332-9.
The nusA gene protein of E. coli is involved in regulating termination of transcription in vivo. In vitro it causes termination of transcription in the tR2 region of the PR operon of bacteriophage lambda. We have now used a nusA-Sepharose affinity column and gradient sedimentation experiments to show that the nusA protein binds directly, with great specificity, and with equimolar stoichiometry to the E. coli RNA polymerase core enzyme beta beta' alpha 2. The RNA polymerase sigma subunit is able to displace the nusA protein from a beta beta' alpha 2-nusA complex, regenerating RNA polymerase holoenzyme beta beta alpha 2-sigma able selectively to initiate transcription at promoter sites. It is proposed that beta beta' alpha 2-nusA and beta beta' alpha 2-sigma are complementary forms of RNA polymerase that interchange with one another in the initiation-termination cycle of transcription.
大肠杆菌的nusA基因蛋白参与体内转录终止的调控。在体外,它能使噬菌体λ的PR操纵子的tR2区域发生转录终止。我们现在使用nusA-琼脂糖亲和柱和梯度沉降实验表明,nusA蛋白能以等摩尔化学计量比直接、高度特异性地与大肠杆菌RNA聚合酶核心酶ββ'α2结合。RNA聚合酶σ亚基能够将nusA蛋白从ββ'α2-nusA复合物中置换出来,再生出能在启动子位点选择性起始转录的RNA聚合酶全酶ββ'α2-σ。有人提出,ββ'α2-nusA和ββ'α2-σ是RNA聚合酶的互补形式,它们在转录的起始-终止循环中相互转换。