Structural insights into transcription activation mechanism of the global regulator GlnR from actinobacteria

Abstract

AbstractGlnR, an OmpR/PhoB subfamily protein, is an orphan response regulator that globally coordinates the expression of genes responsible for nitrogen, carbon and phosphate metabolism in actinobacteria. Although much efforts at biochemical and genetic analyses have been made on the mechanism of GlnR-dependent transcription activation, it still remains unclear owing to lacking the structure of GlnR-dependent transcription activation complex (GlnR-TAC). Here, we report a crystal structure of a binary complex including a C terminal DNA binding domain of GlnR (GlnR_DBD) and its regulatorycis-element DNA, and a cryo-EM structure of GlnR-TAC comprising ofMycobacterium tuberculosisRNA polymerase, GlnR, and a promoter containing four well-characterized conserved GlnR binding sites. These structures show four GlnR protomers coordinately engage promoter DNA in a head-to-tail manner, with two N-terminal receiver domains of GlnR (GlnR-RECs) jointly act as a bridge to connect RNAP αNTD with the upstream GlnR_DBD. GlnR-TAC is stabilized by complex protein-protein interactions between GlnR and the conserved β flap, σAR4, αCTD, αNTD domains of RNAP. These are in good agreement with our mutational and kinetic single-molecule fluorescence assays. Altogether, our results reveal a general transcription activation mechanism for the global regulator GlnR and other OmpR/PhoB subfamily proteins, and present a unique mode of bacterial transcription regulation.Significance statementIn low-GC gram-negative bacteria, the typical two component system NtrB/NtrC accounts for the expression of genes related to nitrogen metabolism. In high-GC gram-positive actinobacteria, GlnR, an atypical and orphan response regulator (RR) of the OmpR/PhoB subfamily proteins, globally coordinates transcription of genes involved in nitrogen, carbon and phosphate metabolism. Here, using crystallography, cryo-electron microscopy, and single-molecule fluorescence assays, we show that GlnR activates transcription by contacting DNA between the −10 and −35 elements and further upstream through contacting σ region 4 and RNAP β flap subunit. We also identify a previously unobserved cooperative engagement of four GlnR protomers to the promoter DNA, which not only makes the transcription initiation complex (RPo) more stable, but also provides better transcription activities.