Differential transcriptional regulation of orthologous dps genes from two closely related heterocyst-forming cyanobacteria

FEMS Microbiol Lett. 2015 Mar;362(6):fnv017. doi: 10.1093/femsle/fnv017. Epub 2015 Feb 5.

Abstract

In cyanobacteria, DNA-binding proteins from starved cells (Dps) play an important role in the cellular response to oxidative and nutritional stresses. In this study, we have characterized the cell-type specificity and the promoter regions of two orthologous dps genes, Npun_R5799 in Nostoc punctiforme and alr3808 in Anabaena sp. PCC 7120. A transcriptional start site (TSS), identical in location to the previously identified proximal TSS of alr3808, was identified for Npun_R5799 under both combined nitrogen supplemented and N2-fixing growth conditions. However, only alr3808 was also transcribed from a second distal TSS. Sequence homologies suggest that the promoter region containing the distal TSS is not conserved upstream of orthologous genes among heterocyst-forming cyanobacteria. The analysis of promoter GFP-reporter strains showed a different role in governing cell-type specificity between the proximal and distal promoter of alr3808. We here confirmed the heterocyst specificity of the distal promoter of alr3808 and described a very early induction of its expression during proheterocyst differentiation. In contrast, the complete promoters of both genes were active in all cells. Even though Npun_R5799 and alr3808 are orthologs, the regulation of their respective expression differs, indicating distinctions in the function of these cyanobacterial Dps proteins depending on the strain and cell type.

Keywords: Anabaena; Cyanobacteria; DIF motif; Nostoc; ROS scavenging; ferritin-like protein; heterocyst differentiation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anabaena / genetics*
  • Anabaena / physiology
  • Bacterial Proteins / genetics*
  • DNA-Binding Proteins / metabolism
  • Gene Expression Regulation, Bacterial*
  • Genes, Bacterial
  • Nitrogen / metabolism
  • Nostoc / genetics*
  • Promoter Regions, Genetic*
  • Sequence Homology
  • Transcription Initiation Site

Substances

  • Bacterial Proteins
  • DNA-Binding Proteins
  • Nitrogen