Energy drives the dynamic localization of cyanobacterial nitrogen regulators during diurnal cycles

Environ Microbiol. 2018 Mar;20(3):1240-1252. doi: 10.1111/1462-2920.14071. Epub 2018 Mar 14.

Abstract

Cyanobacteria, phototrophic organisms performing oxygenic photosynthesis, must adapt their metabolic processes to the challenges imposed by the succession of days and nights. Two conserved cyanobacterial proteins, PII and PipX, function as hubs of the nitrogen interaction network, forming complexes with a variety of diverse targets. While PII proteins are found in all three domains of life as integrators of signals of the nitrogen and carbon balance, PipX proteins are unique to cyanobacteria, where they provide a mechanistic link between PII signalling and the control of gene expression by the global nitrogen regulator NtcA. Here we demonstrate that PII and PipX display distinct localization patterns during diurnal cycles, co-localizing into the same foci at the periphery and poles of the cells during dark periods, a circadian-independent process requiring a low ATP/ADP ratio. Genetic, cellular biology and biochemical approaches used here provide new insights into the nitrogen regulatory network, calling attention to the roles of PII as energy sensors and its interactions with PipX in the context of essential signalling pathways. This study expands the contribution of the nitrogen regulators PII and PipX to integrate and transduce key environmental signals that allow cyanobacteria to thrive in our planet.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Diphosphate / metabolism
  • Adenosine Triphosphate / metabolism
  • Bacterial Proteins / metabolism
  • Carbon / metabolism
  • Circadian Rhythm / genetics*
  • DNA-Binding Proteins / metabolism
  • Energy Metabolism / physiology*
  • Nitrogen / metabolism*
  • PII Nitrogen Regulatory Proteins / metabolism*
  • Signal Transduction / genetics
  • Synechococcus / genetics*
  • Synechococcus / metabolism*
  • Transcription Factors / metabolism
  • Transcription, Genetic / genetics

Substances

  • Bacterial Proteins
  • DNA-Binding Proteins
  • PII Nitrogen Regulatory Proteins
  • Transcription Factors
  • ntcA protein, Synechococcus
  • Adenosine Diphosphate
  • Carbon
  • Adenosine Triphosphate
  • Nitrogen