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Updated: Feb 2, 2026

Using Mycobacterium smegmatis as a Bioindicator for Zinc-Limited Growth Conditions in Mycobacteria
Published on: September 20, 2024
Ms1 RNA increases the amount of RNA polymerase in Mycobacterium smegmatis
Michaela Šiková1, Martina Janoušková1,2, Olga Ramaniuk1
1Laboratory of Microbial Genetics and Gene Expression, Institute of Microbiology, Czech Academy of Sciences, Prague, Czech Republic.
Abstract:
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.
Insights
Ms1, a small RNA in mycobacteria, accumulates during stationary phase and regulates RNA polymerase (RNAP) levels. Its absence hinders RNAP availability, impairing the bacterium's response to environmental shifts.
Area of Science:
- Microbiology
- Molecular Biology
- RNA Biology
Background:
- Ms1 is a small RNA (sRNA) identified in mycobacteria and actinobacteria.
- Unlike 6S RNA, Ms1 interacts with the RNA polymerase (RNAP) core, not holoenzyme.
Purpose of the Study:
- To investigate the role and regulation of Ms1 in Mycobacterium smegmatis.
- To understand Ms1's impact on RNAP levels and bacterial response to environmental changes.
Main Methods:
- Transcriptome analysis (RNA-seq) of wild-type and ΔMs1 strains.
- Identification of Ms1 promoter (PMs1) and regulatory elements.
- Enzyme activity assays involving PNPase (an RNase).
Main Results:
- Ms1 is the most abundant non-rRNA transcript in stationary phase M. smegmatis.
- Ms1 accumulation is due to high synthesis and low degradation, influenced by PNPase.
- Absence of Ms1 leads to reduced intracellular RNAP levels (mRNA and protein) for β and β' subunits.
- ΔMs1 strain exhibits impaired response to environmental changes during outgrowth.
Conclusions:
- Ms1 plays a crucial role in regulating RNAP availability in stationary phase.
- Ms1 is essential for M. smegmatis to adapt to changing environmental conditions.
- Ms1's regulation of RNAP impacts bacterial fitness and stress response.
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