Acclimation of Oxygenic Photosynthesis to Iron Starvation Is Controlled by the sRNA IsaR1

Curr Biol. 2017 May 22;27(10):1425-1436.e7. doi: 10.1016/j.cub.2017.04.010. Epub 2017 May 4.

Abstract

Oxygenic photosynthesis crucially depends on proteins that possess Fe2+ or Fe/S complexes as co-factors or prosthetic groups. Here, we show that the small regulatory RNA (sRNA) IsaR1 (Iron-Stress-Activated RNA 1) plays a pivotal role in acclimation to low-iron conditions. The IsaR1 regulon consists of more than 15 direct targets, including Fe2+-containing proteins involved in photosynthetic electron transfer, detoxification of anion radicals, citrate cycle, and tetrapyrrole biogenesis. IsaR1 is essential for maintaining physiological levels of Fe/S cluster biogenesis proteins during iron deprivation. Consequently, IsaR1 affects the acclimation of the photosynthetic apparatus to iron starvation at three levels: (1) directly, via posttranscriptional repression of gene expression; (2) indirectly, via suppression of pigment; and (3) Fe/S cluster biosynthesis. Homologs of IsaR1 are widely conserved throughout the cyanobacterial phylum. We conclude that IsaR1 is a critically important riboregulator. These findings provide a new perspective for understanding the regulation of iron homeostasis in photosynthetic organisms.

Keywords: Fe/S cluster biogenesis; Synechocystis; cytochrome b(6)f complex; electron transfer; ferredoxin I; iron homeostasis; photosynthesis; regulatory sRNA.

MeSH terms

  • Acclimatization
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism
  • Cyanobacteria / genetics
  • Cyanobacteria / physiology*
  • Gene Expression Profiling
  • Homeostasis
  • Iron Deficiencies*
  • Iron-Sulfur Proteins / genetics
  • Iron-Sulfur Proteins / metabolism
  • Oxygen / metabolism*
  • Photosynthesis / physiology*
  • RNA, Bacterial / genetics
  • RNA, Small Untranslated / genetics*
  • Transcription, Genetic
  • Transcriptome

Substances

  • Bacterial Proteins
  • Iron-Sulfur Proteins
  • RNA, Bacterial
  • RNA, Small Untranslated
  • Oxygen