| Literature DB >> 27858580 |
Toomas Mets1, Markus Lippus1, David Schryer1, Aivar Liiv2, Villu Kasari1, Anton Paier1, Ülo Maiväli1, Jaanus Remme2, Tanel Tenson1, Niilo Kaldalu1.
Abstract
The endoribonuclease toxins of the E. coli toxin-antitoxin systems arrest bacterial growth and protein synthesis by targeting cellular mRNAs. As an exception, E. coli MazF was reported to cleave also 16S rRNA at a single site and separate an anti-Shine-Dalgarno sequence-containing RNA fragment from the ribosome. We noticed extensive rRNA fragmentation in response to induction of the toxins MazF and MqsR, which suggested that these toxins can cleave rRNA at multiple sites. We adapted differential RNA-sequencing to map the toxin-cleaved 5'- and 3'-ends. Our results show that the MazF and MqsR cleavage sites are located within structured rRNA regions and, therefore, are not accessible in assembled ribosomes. Most of the rRNA fragments are located in the aberrant ribosomal subunits that accumulate in response to toxin induction and contain unprocessed rRNA precursors. We did not detect MazF- or MqsR-cleaved rRNA in stationary phase bacteria and in assembled ribosomes. Thus, we conclude that MazF and MqsR cleave rRNA precursors before the ribosomes are assembled and potentially facilitate the decay of surplus rRNA transcripts during stress.Entities:
Keywords: Differential RNA sequencing; MazF; MqsR; Toxin-Antitoxin systems; rRNA precursors; ribosome
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Year: 2016 PMID: 27858580 PMCID: PMC5270532 DOI: 10.1080/15476286.2016.1259784
Source DB: PubMed Journal: RNA Biol ISSN: 1547-6286 Impact factor: 4.652