Region 3.2 of the factor controls the stability of rRNA promoter complexes and potentiates their repression by DksA

Danil Pupov, Ivan Petushkov, Daria Esyunina, Katsuhiko S. Murakami, Andrey Kulbachinskiy

Research output: Contribution to journalArticle

3 Scopus citations

Abstract

The factor drives promoter recognition by bacterial RNA polymerase (RNAP) and is also essential for later steps of transcription initiation, including RNA priming and promoter escape. Conserved region 3.2 of the primary factor (‘ finger’) directly contacts the template DNA strand in the open promoter complex and facilitates initiating NTP binding in the active center of RNAP. Ribosomal RNA promoters are responsible for most RNA synthesis during exponential growth but should be silenced during the stationary phase to save cell resources. In Escherichia coli, the silencing mainly results from the action of the secondary channel factor DksA, which together with ppGpp binds RNAP and dramatically decreases the stability of intrinsically unstable rRNA promoter complexes. We demonstrate that this switch depends on the finger that destabilizes RNAP–promoter interactions. Mutations in the finger moderately decrease initiating NTP binding but significantly increase promoter complex stability and reduce DksA affinity to the RNAP–rRNA promoter complex, thus making rRNA transcription less sensitive to DksA/ppGpp both in vitro and in vivo. Thus, destabilization of rRNA promoter complexes by the finger makes them a target for robust regulation by the stringent response factors under stress conditions.

Original languageEnglish (US)
Pages (from-to)11477-11487
Number of pages11
JournalNucleic acids research
Volume46
Issue number21
DOIs
StatePublished - 2018

All Science Journal Classification (ASJC) codes

  • Genetics

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