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Ms1 RNA increases the amount of RNA polymerase in Mycobacterium smegmatis
Author(s) -
Šiková Michaela,
Janoušková Martina,
Ramaniuk Olga,
Páleníková Petra,
Pospíšil Jiří,
Bartl Pavel,
Suder Agnieszka,
Pajer Petr,
Kubičková Pavla,
Pavliš Ota,
Hradilová Miluše,
Vítovská Dragana,
Šanderová Hana,
Převorovský Martin,
Hnilicová Jarmila,
Krásný Libor
Publication year - 2019
Publication title -
molecular microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.857
H-Index - 247
eISSN - 1365-2958
pISSN - 0950-382X
DOI - 10.1111/mmi.14159
Subject(s) - biology , rna polymerase , mycobacterium smegmatis , sigma factor , rnase p , rna , gene , rna dependent rna polymerase , transcription (linguistics) , stringent response , polymerase , microbiology and biotechnology , biochemistry , escherichia coli , mycobacterium tuberculosis , medicine , tuberculosis , linguistics , philosophy , pathology
Summary 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, P Ms1 , 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 Δ Ms1 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 Δ Ms1 strain has a smaller pool of RNAPs available when the transcriptional demand increases. This contributes to the inability of the Δ Ms1 strain to rapidly react to environmental changes during outgrowth from stationary phase.