Ms1 RNA increases the amount of RNA polymerase in Mycobacterium smegmatis
Language English Country Great Britain, England Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
Grant support
13-27150P
Czech Science Foundation - International
P305/12/G034
Czech Science Foundation - International
946216
Charles University - International
VI20152020044
Ministry of the Interior of the Czech Republic - International
CZ.02.1.01/0.0/0.0/16_019/0000778
Ministry of Education, Youth and Sports of the Czech Republic within project the Center for advanced applied science - International
CZ.02.1.01/0.0/0.0/16_019/0000778
Ministry of Education, Youth and Sports of the Czech Republic - International
PubMed
30427073
DOI
10.1111/mmi.14159
Knihovny.cz E-resources
- MeSH
- RNA, Bacterial metabolism MeSH
- Gene Deletion MeSH
- DNA-Directed RNA Polymerases metabolism MeSH
- RNA, Small Untranslated genetics metabolism MeSH
- Mycobacterium smegmatis enzymology genetics growth & development metabolism MeSH
- Gene Expression Profiling MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- RNA, Bacterial MeSH
- DNA-Directed RNA Polymerases MeSH
- RNA, Small Untranslated MeSH
Ms1 is a sRNA recently found in mycobacteria and several other actinobacterial species. Ms1 interacts with the RNA polymerase (RNAP) core devoid of sigma factors, which differs from 6S RNA that binds to RNAP holoenzymes containing the primary sigma factor. Here we show that Ms1 is the most abundant non-rRNA transcript in stationary phase in Mycobacterium smegmatis. The accumulation of Ms1 stems from its high-level synthesis combined with decreased degradation. We identify the Ms1 promoter, PMs1 , and cis-acting elements important for its activity. Furthermore, we demonstrate that PNPase (an RNase) contributes to the differential accumulation of Ms1 during growth. Then, by comparing the transcriptomes of wt and ΔMs1 strains from stationary phase, we reveal that Ms1 affects the intracellular level of RNAP. The absence of Ms1 results in decreased levels of the mRNAs encoding β and β' subunits of RNAP, which is also reflected at the protein level. Thus, the ΔMs1 strain has a smaller pool of RNAPs available when the transcriptional demand increases. This contributes to the inability of the ΔMs1 strain to rapidly react to environmental changes during outgrowth from stationary phase.
Faculty of Science Department of Cell Biology Charles University Prague Czech Republic
Faculty of Science Department of Genetics and Microbiology Charles University Prague Czech Republic
Military Health Institute Military Medical Agency Prague Czech Republic
References provided by Crossref.org
MoaB2, a newly identified transcription factor, binds to σA in Mycobacterium smegmatis
Mycobacterial HelD connects RNA polymerase recycling with transcription initiation
RIP-seq reveals RNAs that interact with RNA polymerase and primary sigma factors in bacteria
6S-Like scr3559 RNA Affects Development and Antibiotic Production in Streptomyces coelicolor
The torpedo effect in Bacillus subtilis: RNase J1 resolves stalled transcription complexes