PLoS ONE · 2016 · 19 citations · 44 references
Life SciencesMicrobiologyMolecular BiologyGenomicsMicrobial GeneticsRna ProcessingRna InterferenceRna StructureTranslation In ProkaryotesCleavageCleavage Site IdentificationCleavage SpecificityParallel SequencingProtease Cleavage SpecificityPseudomonas SpeciesSequence-selective CleavageSequence-specific Rna Cleavage
Under environmental stress, microbes are known to alter their translation patterns using sequence-specific endoribonucleases that we call RNA interferases. However, there has been limited insight regarding which RNAs are specifically cleaved by these RNA interferases, hence their physiological functions remain unknown. In the current study, we developed a novel method to effectively identify cleavage specificities with massive parallel sequencing. This approach uses artificially designed RNAs composed of diverse sequences, which do not form extensive secondary structures, and it correctly identified the cleavage sequence of a well-characterized Escherichia coli RNA interferase, MazF, as ACA. In addition, we also determined that an uncharacterized MazF homologue isolated from Pseudomonas putida specifically recognizes the unique triplet, UAC. Using a real-time fluorescence resonance energy transfer assay, the UAC triplet was further proved to be essential for cleavage in P. putida MazF. These results highlight an effective method to determine cleavage specificity of RNA interferases.
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WebLogo: A Sequence Logo Generator: Figure 1
Gavin E. Crooks, Gary C. Hon, John‐Marc Chandonia et al. · Genome Research · 2004 · 13K citations · Full text
Elias Aizenman, Hanna Engelberg–Kulka, Gad Glaser · Proceedings of the National Academy of Sciences · 1996 · 602 citations