Structures of Class I and Class II Transcription Complexes Reveal the Molecular Basis of RamA-Dependent Transcription Activation

Transcription activator RamA is linked to multidrug resistance of Klebsiella pneumoniae through controlling genes that encode efflux pumps (acrA) and porin-regulating antisense RNA (micF). In bacteria, sigma(70), together with activators, controls the majority of genes by recruiting RNA polymerase (RNAP) to the promoter regions. RNAP and sigma(70) form a holoenzyme that recognizes -35 and -10 promoter DNA consensus sites. Many activators bind upstream from the holoenzyme and can be broadly divided into two classes. RamA acts as a class I activator on acrA and class II activator on micF, respectively. The authors present biochemical and structural data on RamA in complex with RNAP-sigma(70) at the two promoters and the data reveal the molecular basis for how RamA assembles and interacts with core RNAP and activates transcription that contributes to antibiotic resistance. Further, comparing with CAP/TAP complexes reveals common and activator-specific features in activator binding and uncovers distinct roles of the two C-terminal domains of RNAP alpha subunit.

Automated summary

Transcription activator RamA is linked to multidrug resistance of Klebsiella pneumoniae by controlling key genes that encode efflux pumps and porin-regulating antisense RNA. The interaction between RamA and RNAP-sigma(70) at promoter regions reveals the molecular basis for how RamA activates transcription contributing to antibiotic resistance. Comparisons with CAP/TAP complexes uncover common and activator-specific features in activator binding and reveal distinct roles of the two C-terminal domains of RNAP alpha subunit.