A c-di-AMP riboswitch controlling kdpFABC operon transcription regulates the potassium transporter system in Bacillus thuringiensis

Commun Biol. 2019 Apr 29:2:151. doi: 10.1038/s42003-019-0414-6. eCollection 2019.

Abstract

The intracellular K+ level in bacteria is strictly controlled by K+ uptake and efflux systems. Among these, KdpFABC is a high-affinity K+ transporter system that is generally activated by the KdpDE two-component system in response to K+ limitation stress. However, the regulatory mechanism remains obscure in bacteria lacking the kdpDE genes. Here we report that the transcription of a kdpFABC operon is distinctively regulated by a cyclic diadenylate monophosphate (c-di-AMP) riboswitch located at the 5'-untranslated region of kdp transcript, and binding of c-di-AMP to the riboswitch promotes its intrinsic termination that blocks the kdpFABC transcription. Further, the intracellular c-di-AMP concentration was found to decrease under the K+ limitation stress, leading to transcriptional read-through over the terminator to allow kdpFABC expression. This regulatory element is found predominantly in the Bacillus cereus group and correlate well with the K+ and c-di-AMP homeostasis that affects a variety of crucial cellular functions.

Keywords: Bacterial genes; Riboswitches.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphatases / genetics
  • Adenosine Triphosphatases / metabolism
  • Bacillus thuringiensis / genetics*
  • Bacillus thuringiensis / metabolism
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism
  • Base Sequence
  • Cation Transport Proteins / genetics
  • Cation Transport Proteins / metabolism
  • Dinucleoside Phosphates / metabolism*
  • Gene Expression Regulation, Bacterial*
  • Ion Transport
  • Isoenzymes / genetics
  • Isoenzymes / metabolism
  • Operon*
  • Potassium / metabolism*
  • Protein Kinases / genetics
  • Protein Kinases / metabolism
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Riboswitch*
  • Sequence Alignment
  • Trans-Activators / genetics
  • Trans-Activators / metabolism
  • Transcription, Genetic*

Substances

  • Bacterial Proteins
  • Cation Transport Proteins
  • Dinucleoside Phosphates
  • Isoenzymes
  • RNA, Messenger
  • Riboswitch
  • Trans-Activators
  • cyclic diadenosine phosphate
  • Protein Kinases
  • kdpD protein, Bacteria
  • Adenosine Triphosphatases
  • Potassium