The hok mRNA family

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Item Type:	Article
Title:	The hok mRNA family
Creators Name:	Steif, A. and Meyer, I.M.
Abstract:	The hok/sok toxin-antitoxin system of Escherichia coli plasmid R1 increases plasmid maintenance by killing plasmid-free daughter cells. The hok/sok locus specifies two RNAs: hok mRNA, which encodes a toxic transmembrane protein, and sok antisense RNA, which binds a complementary region in the hok mRNA and induces transcript degradation. During cell growth, the cis-encoded sok RNA inhibits expression of the Hok toxin. In plasmid-free segregants, the rapid decay of sok RNA relative to hok mRNA permits Hok translation, leading to cell death. This post-segregational killing mechanism relies upon the ability of the hok mRNA to adopt alternative structural configurations, which affect ease of translation and the susceptibility of the molecule to degradation. The full-length hok transcript is stable, highly structured and immune to ribosome and antisense RNA binding. Gradual 3' end processing produces dramatic structural rearrangements in the mRNA, which render the molecule translationally active and expose the sok RNA binding site. During transcription, premature ribosome and sok binding are prevented through the formation of transient metastable hairpins in the 5' end of the nascent transcript. Several hok mRNA paralogs have been identified in the genome of E. coli, and Hok protein orthologs found in the genomes of Enterobacteria. Using a combination of automated search and extensive manual editing, we compiled a multiple sequence alignment for the hok mRNA. All three experimentally validated hok mRNA structures are mapped onto this alignment, which has been submitted to the Rfam database for RNA families.
Keywords:	Hok/sok, Toxin-Antitoxin System, Post-Segregational Killing, Co-transcriptional RNA Folding, Transient RNA Structures, Mutually Exclusive RNA Structures, RNA Structures Regulating Gene Expression
Source:	RNA Biology
ISSN:	1547-6286
Publisher:	Landes Bioscience
Volume:	9
Number:	12
Page Range:	1399-1404
Date:	1 December 2012
Official Publication:	https://doi.org/10.4161/rna.22746
PubMed:	View item in PubMed

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