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1.
PLoS Genet ; 15(2): e1007646, 2019 02.
Article in English | MEDLINE | ID: mdl-30742606

ABSTRACT

Putrescine belongs to the large group of polyamines, an essential class of metabolites that exists throughout all kingdoms of life. The Salmonella speF gene encodes an inducible ornithine decarboxylase that produces putrescine from ornithine. Putrescine can be also synthesized from arginine in a parallel metabolic pathway. Here, we show that speF expression is controlled at multiple levels through regulatory elements contained in a long leader sequence. At the heart of this regulation is a short open reading frame, orf34, which is required for speF production. Translation of orf34 interferes with Rho-dependent transcription termination and helps to unfold an inhibitory RNA structure sequestering speF ribosome-binding site. Two consecutive arginine codons in the conserved domain of orf34 provide a third level of speF regulation. Uninterrupted translation of orf34 under conditions of high arginine allows the formation of a speF mRNA structure that is degraded by RNase G, whereas ribosome pausing at the consecutive arginine codons in the absence of arginine enables the formation of an alternative structure that is resistant to RNase G. Thus, the rate of ribosome progression during translation of the upstream ORF influences the dynamics of speF mRNA folding and putrescine production. The identification of orf34 and its regulatory functions provides evidence for the evolutionary conservation of ornithine decarboxylase regulatory elements and putrescine production.


Subject(s)
Arginine/metabolism , Polyamines/metabolism , RNA, Messenger/genetics , Salmonella/genetics , Salmonella/metabolism , Base Sequence , Open Reading Frames/genetics , Ornithine/metabolism , Ornithine Decarboxylase/metabolism , Protein Biosynthesis/genetics , Protein Domains/physiology , Transcription Termination, Genetic/physiology
3.
PLoS Genet ; 12(4): e1005975, 2016 Apr.
Article in English | MEDLINE | ID: mdl-27057757

ABSTRACT

While an increasing number of conserved small regulatory RNAs (sRNAs) are known to function in general bacterial physiology, the roles and modes of action of sRNAs from horizontally acquired genomic regions remain little understood. The IsrK sRNA of Gifsy-1 prophage of Salmonella belongs to the latter class. This regulatory RNA exists in two isoforms. The first forms, when a portion of transcripts originating from isrK promoter reads-through the IsrK transcription-terminator producing a translationally inactive mRNA target. Acting in trans, the second isoform, short IsrK RNA, binds the inactive transcript rendering it translationally active. By switching on translation of the first isoform, short IsrK indirectly activates the production of AntQ, an antiterminator protein located upstream of isrK. Expression of antQ globally interferes with transcription termination resulting in bacterial growth arrest and ultimately cell death. Escherichia coli and Salmonella cells expressing AntQ display condensed chromatin morphology and localization of UvrD to the nucleoid. The toxic phenotype of AntQ can be rescued by co-expression of the transcription termination factor, Rho, or RNase H, which protects genomic DNA from breaks by resolving R-loops. We propose that AntQ causes conflicts between transcription and replication machineries and thus promotes DNA damage. The isrK locus represents a unique example of an island-encoded sRNA that exerts a highly complex regulatory mechanism to tune the expression of a toxic protein.


Subject(s)
Gene Expression Regulation, Bacterial/genetics , Prophages/genetics , RNA, Messenger/genetics , RNA, Small Untranslated/genetics , Regulatory Sequences, Ribonucleic Acid/genetics , Salmonella typhimurium/genetics , Bacterial Proteins/genetics , Bacteriophages/genetics , DNA, Bacterial/genetics , Escherichia coli/genetics , Mutagenesis , Open Reading Frames/genetics , Promoter Regions, Genetic , RNA Isoforms/genetics , RNA, Bacterial/genetics , Rho Factor/metabolism , Ribonuclease H/metabolism , Salmonella typhimurium/growth & development , Salmonella typhimurium/metabolism , Transcription, Genetic/genetics , Viral Proteins/genetics
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