RNA sequence requirements for NasR-mediated, nitrate-responsive transcription antitermination of the Klebsiella oxytoca M5al nasF operon leader

J Mol Biol. 1999 Sep 17;292(2):203-16. doi: 10.1006/jmbi.1999.3084.

Abstract

In Klebsiella oxytoca, enzymes required for nitrate assimilation are encoded by the nasFEDCBA operon. Nitrate and nitrite induction of nasF operon expression is determined by a transcriptional antitermination mechanism, in which the nasR gene product responds to nitrate or nitrite and overcomes transcription termination at the factor-independent terminator site located in the nasF upstream leader region. Previous studies led to the hypothesis that the NasR protein mediates transcription antitermination through interaction with nasF leader RNA. Here, we report a DNA sequence comparison that reveals conserved 1:2 and 3:4 RNA secondary structures in the nasF leader RNAs from two Klebsiella species. Additionally, we found that specific binding of the NasR protein to nasF leader RNA was stimulated by nitrate and nitrite. We combined mutational analysis, in vivo and in vitro antitermination assays, and an RNA electrophoretic mobility shift assay to define regions in the nasF leader that are essential for antitermination and for NasR-RNA interaction. Formation of the 1:2 stem structure and the specific sequence of the 1:2 hexanucleotide loop were required for both nitrate induction and for NasR-RNA interaction. Mutations in the 1:2 stem-loop region that abolished nitrate induction also interfered with NasR-leader RNA interaction. Finally, nucleotide alterations or additions in the linker region between the 1:2 and 3:4 stem-loops were deleterious to nasF operon induction but not to NasR-leader RNA interaction. We hypothesize that NasR protein recognizes the 1:2 stem-loop structure in the nasF leader RNA to mediate transcription antitermination in response to nitrate or nitrite.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Bacterial Proteins / genetics
  • Base Sequence
  • Carrier Proteins / genetics*
  • Gene Expression Regulation, Bacterial / genetics*
  • Genes, Reporter
  • Klebsiella / genetics*
  • Molecular Sequence Data
  • Mutation
  • Nitrates / metabolism*
  • Nitrites / metabolism
  • Nucleic Acid Conformation
  • Operon / genetics
  • Periplasmic Binding Proteins*
  • Phylogeny
  • Protein Binding
  • Pseudomonas aeruginosa / genetics
  • RNA / genetics*
  • RNA, Bacterial / genetics
  • RNA-Binding Proteins / genetics
  • Recombinant Proteins / metabolism
  • Sequence Homology

Substances

  • Bacterial Proteins
  • Carrier Proteins
  • NasF protein, Klebsiella oxytoca
  • Nitrates
  • Nitrites
  • Periplasmic Binding Proteins
  • RNA, Bacterial
  • RNA-Binding Proteins
  • Recombinant Proteins
  • RNA

Associated data

  • GENBANK/AF038047