Watnick R S, Gottesman M E
Department of Biochemistry and Molecular Biophysics, College of Physicians and Surgeons, Columbia University, New York, NY 10032, USA.
Proc Natl Acad Sci U S A. 1998 Feb 17;95(4):1546-51. doi: 10.1073/pnas.95.4.1546.
The Nun protein of phage HK022 is an RNA binding protein of the arginine-rich motif family. Nun binds the phage lambda boxB RNA sequence (BOXB) on nascent lambda transcripts and arrests transcription elongation. Binding to BOXB is inhibited by Zn2+ and stimulated by the Escherichia coli NusA protein. Deletion of the Nun C-terminal region enhances BOXB binding and makes it independent of Zn2+ and NusA. The C terminus of Nun thus appears to interfere with the N-terminal RNA binding motif. NusA relieves this interference by binding to the Nun C terminus and forming a complex with Nun and BOXB. However, NusA also inhibits transcription arrest in vitro, in the absence of the other Nus factors. Nun deleted for its C terminus fails to bind RNA polymerase (RNAP) (RNAP) or NusA in vitro or to arrest transcription in vivo or in vitro. Our findings are consistent with the idea that NusA inhibits transcription arrest by binding to the Nun C terminus, thus blocking the interaction between Nun and RNAP. NusG, NusB, and NusE factors restore transcription arrest, presumably by promoting transfer of Nun from NusA to RNAP.
噬菌体HK022的Nun蛋白是富含精氨酸基序家族的一种RNA结合蛋白。Nun与新生λ转录本上的噬菌体λ boxB RNA序列(BOXB)结合,并阻止转录延伸。与BOXB的结合受到Zn2+的抑制,并受到大肠杆菌NusA蛋白的刺激。Nun C末端区域的缺失增强了与BOXB的结合,并使其独立于Zn2+和NusA。因此,Nun的C末端似乎会干扰N末端的RNA结合基序。NusA通过与Nun C末端结合并与Nun和BOXB形成复合物来解除这种干扰。然而,在没有其他Nus因子的情况下,NusA在体外也会抑制转录终止。缺失C末端的Nun在体外无法结合RNA聚合酶(RNAP)或NusA,在体内或体外均无法阻止转录。我们的研究结果与以下观点一致,即NusA通过与Nun C末端结合来抑制转录终止,从而阻断Nun与RNAP之间的相互作用。NusG、NusB和NusE因子可恢复转录终止,推测是通过促进Nun从NusA转移至RNAP来实现的。