Regulation of intracellular free calcium concentration during heterocyst differentiation by HetR and NtcA in Anabaena sp. PCC 7120

Proc Natl Acad Sci U S A. 2006 Jul 25;103(30):11334-9. doi: 10.1073/pnas.0602839103. Epub 2006 Jul 18.

Abstract

Calcium ions are important to some prokaryotic cellular processes, such as heterocyst differentiation of cyanobacteria. Intracellular free Ca(2+)concentration, [Ca(2+)](i), increases several fold in heterocysts and is regulated by CcbP, a Ca(2+)-binding protein found in heterocyst-forming cyanobacteria. We demonstrate here that CcbP is degraded by HetR, a serine-type protease that controls heterocyst differentiation. The degradation depends on Ca(2+) and appears to be specific because HetR did not digest other tested proteins. CcbP was found to bind two Ca(2+) per molecule with K(D) values of 200 nM and 12.8 microM. Degradation of CcbP releases bound Ca(2+) that contributes significantly to the increase of [Ca(2+)](i) during the process of heterocyst differentiation in Anabaena sp. strain PCC 7120. We suggest that degradation of CcbP is a mechanism of positive autoregulation of HetR. The down-regulation of ccbP in differentiating cells and mature heterocysts, which also is critical to the regulation of [Ca(2+)](i), depends on NtcA. Coexpression of ntcA and a ccbP promoter-controlled gfp in Escherichia coli diminished production of GFP, and the decrease is enhanced by alpha-ketoglutarate. It was also found that NtcA could bind a fragment of the ccbP promoter containing an NtcA-binding sequence in a alpha-ketoglutarate-dependent fashion. Therefore, [Ca(2+)](i) is regulated by a collaboration of HetR and NtcA in heterocyst differentiation in Anabaena sp. strain PCC 7120.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anabaena / metabolism*
  • Bacterial Proteins / physiology*
  • Calcium / metabolism*
  • DNA / chemistry
  • DNA-Binding Proteins / physiology*
  • Down-Regulation
  • Escherichia coli / metabolism
  • Gene Expression Regulation, Bacterial*
  • Genes, Bacterial
  • Green Fluorescent Proteins / metabolism
  • Kinetics
  • Protein Binding
  • Serine Endopeptidases / chemistry
  • Time Factors
  • Transcription Factors / physiology*

Substances

  • Bacterial Proteins
  • DNA-Binding Proteins
  • Transcription Factors
  • HetR protein, Bacteria
  • Green Fluorescent Proteins
  • ntcA protein, Synechococcus
  • DNA
  • Serine Endopeptidases
  • Calcium