PipX, the coactivator of NtcA, is a global regulator in cyanobacteria

Proc Natl Acad Sci U S A. 2014 Jun 10;111(23):E2423-30. doi: 10.1073/pnas.1404097111. Epub 2014 May 27.

Abstract

To modulate the expression of genes involved in nitrogen assimilation, the cyanobacterial PII-interacting protein X (PipX) interacts with the global transcriptional regulator NtcA and the signal transduction protein PII, a protein found in all three domains of life as an integrator of signals of the nitrogen and carbon balance. PipX can form alternate complexes with NtcA and PII, and these interactions are stimulated and inhibited, respectively, by 2-oxoglutarate, providing a mechanistic link between PII signaling and NtcA-regulated gene expression. Here, we demonstrate that PipX is involved in a much wider interaction network. The effect of pipX alleles on transcript levels was studied by RNA sequencing of S. elongatus strains grown in the presence of either nitrate or ammonium, followed by multivariate analyses of relevant mutant/control comparisons. As a result of this process, 222 genes were classified into six coherent groups of differentially regulated genes, two of which, containing either NtcA-activated or NtcA-repressed genes, provided further insights into the function of NtcA-PipX complexes. The remaining four groups suggest the involvement of PipX in at least three NtcA-independent regulatory pathways. Our results pave the way to uncover new regulatory interactions and mechanisms in the control of gene expression in cyanobacteria.

Keywords: nitrogen regulation; photosynthesis; transcription; translation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Ammonium Compounds / metabolism
  • Ammonium Compounds / pharmacology
  • Bacterial Proteins / genetics*
  • Bacterial Proteins / metabolism
  • Base Sequence
  • DNA-Binding Proteins / genetics*
  • DNA-Binding Proteins / metabolism
  • Gene Expression Profiling / classification
  • Gene Expression Regulation, Bacterial*
  • Ketoglutaric Acids / pharmacology
  • Models, Genetic
  • Molecular Sequence Data
  • Multivariate Analysis
  • Mutation
  • Nitrates / metabolism
  • Nitrates / pharmacology
  • Nitrogen / metabolism
  • Nitrogen / pharmacology
  • Nucleotide Motifs / genetics
  • PII Nitrogen Regulatory Proteins / genetics
  • PII Nitrogen Regulatory Proteins / metabolism
  • Promoter Regions, Genetic / genetics
  • Protein Binding / drug effects
  • Sequence Homology, Nucleic Acid
  • Synechococcus / genetics*
  • Synechococcus / metabolism
  • Transcription Factors / genetics*
  • Transcription Factors / metabolism
  • Transcription Initiation Site

Substances

  • Ammonium Compounds
  • Bacterial Proteins
  • DNA-Binding Proteins
  • Ketoglutaric Acids
  • Nitrates
  • PII Nitrogen Regulatory Proteins
  • Transcription Factors
  • ntcA protein, Synechococcus
  • Nitrogen