Vassylyeva Marina N, Svetlov Vladimir, Dearborn Altaira D, Klyuyev Sergiy, Artsimovitch Irina, Vassylyev Dmitry G
Department of Biochemistry and Molecular Genetics, Schools of Medicine and Dentistry, University of Alabama at Birmingham, Birmingham, Alabama 35294, USA.
EMBO Rep. 2007 Nov;8(11):1038-43. doi: 10.1038/sj.embor.7401079. Epub 2007 Oct 5.
Bacterial Gre transcript cleavage factors stimulate the intrinsic endonucleolytic activity of RNA polymerase (RNAP) to rescue stalled transcription complexes. They bind to RNAP and extend their coiled-coil (CC) domains to the catalytic centre through the secondary channel. Three existing models for the Gre-RNAP complex postulate congruent mechanisms of Gre-assisted catalysis, while offering conflicting views of the Gre-RNAP interactions. Here, we report the GreB structure of Escherichia coli. The GreB monomers form a triangle with the tip of the amino-terminal CC of one molecule trapped within the hydrophobic cavity of the carboxy-terminal domain of a second molecule. This arrangement suggests an analogous model for recruitment to RNAP. Indeed, the beta'-subunit CC located at the rim of the secondary channel has conserved hydrophobic residues at its tip. We show that substitutions of these residues and those in the GreB C-terminal domain cavity confer defects in GreB activity and binding to RNAP, and present a plausible model for the RNAP-GreB complex.
细菌Gre转录切割因子可刺激RNA聚合酶(RNAP)的内在核酸内切酶活性,以挽救停滞的转录复合物。它们与RNAP结合,并通过二级通道将其卷曲螺旋(CC)结构域延伸至催化中心。关于Gre-RNAP复合物的三种现有模型假定了Gre辅助催化的一致机制,同时对Gre-RNAP相互作用提出了相互矛盾的观点。在此,我们报道了大肠杆菌的GreB结构。GreB单体形成一个三角形,其中一个分子氨基末端CC的尖端被困在第二个分子羧基末端结构域的疏水腔内。这种排列提示了一种类似的募集到RNAP的模型。实际上,位于二级通道边缘的β'-亚基CC在其尖端具有保守的疏水残基。我们表明,这些残基以及GreB C末端结构域腔内残基的取代会导致GreB活性和与RNAP结合的缺陷,并提出了一个关于RNAP-GreB复合物的合理模型。