Impact of Hfq on the Bacillus subtilis transcriptome

PLoS One. 2014 Jun 16;9(6):e98661. doi: 10.1371/journal.pone.0098661. eCollection 2014.

Abstract

The RNA chaperone Hfq acts as a central player in post-transcriptional gene regulation in several Gram-negative Bacteria, whereas comparatively little is known about its role in Gram-positive Bacteria. Here, we studied the function of Hfq in Bacillus subtilis, and show that it confers a survival advantage. A comparative transcriptome analysis revealed mRNAs with a differential abundance that are governed by the ResD-ResE system required for aerobic and anaerobic respiration. Expression of resD was found to be up-regulated in the hfq- strain. Furthermore, several genes of the GerE and ComK regulons were de-regulated in the hfq- background. Surprisingly, only six out of >100 known and predicted small RNAs (sRNAs) showed altered abundance in the absence of Hfq. Moreover, Hfq positively affected the transcript abundance of genes encoding type I toxin-antitoxin systems. Taken the moderate effect on sRNA levels and mRNAs together, it seems rather unlikely that Hfq plays a central role in RNA transactions in Bacillus subtilis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aerobiosis
  • Bacillus subtilis / genetics
  • Bacillus subtilis / growth & development*
  • Bacillus subtilis / metabolism
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism*
  • DNA-Binding Proteins / genetics
  • Gene Expression Profiling / methods*
  • Gene Expression Regulation, Bacterial*
  • Host Factor 1 Protein / genetics
  • Host Factor 1 Protein / metabolism*
  • RNA, Bacterial / analysis*
  • RNA, Messenger / analysis
  • RNA, Small Nuclear / analysis
  • Regulon
  • Stress, Physiological
  • Transcription Factors / genetics

Substances

  • Bacterial Proteins
  • DNA-Binding Proteins
  • Host Factor 1 Protein
  • RNA, Bacterial
  • RNA, Messenger
  • RNA, Small Nuclear
  • ResD protein, Bacillus subtilis
  • Transcription Factors

Grants and funding

The work was supported by the Austrian Science Fund (www.fwf.ac.at/en) through the Special Research Program RNA-REG F43, subproject AF4311 (UB), and the doctoral program RNA-Biology W-1207 (HH). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.