
AbstractThe RNA chaperone Hfq acting as a hexamer, is a known mediator of post-transcriptional regulation expediting basepairing between small RNAs (sRNAs) and their target mRNAs. However, the intricate details associated with Hfq-RNA biogenesis are still unclear. Previously, we reported that the stringent response regulator, RelA is a functional partner of Hfq that facilitates Hfq-mediated sRNA-mRNA regulationin vivoand induces Hfq hexamerizationin vitro. Here, for the first time we show that RelA-mediated Hfq hexamerization requires an initial binding of RNA, preferably sRNA to Hfq monomers. By interacting with a Shine-Dalgarno-like sequence (GGAG) in the sRNA, RelA stabilizes the initially unstable complex of RNA bound-Hfq monomer, enabling the attachment of more Hfq subunits to form a functional hexamer. Overall, our study showing that RNA binding to Hfq monomers is at the heart of RelA-mediated Hfq hexamerization, challenges the previous concept that only Hfq hexamers can bind RNA.
Base Sequence, Protein Stability, Science, Escherichia coli Proteins, Q, Host Factor 1 Protein, Models, Biological, Article, GTP Pyrophosphokinase, Protein Subunits, RNA, Bacterial, Amino Acid Substitution, Escherichia coli, RNA, Small Untranslated, Protein Multimerization, Protein Structure, Quaternary, Protein Binding, Sequence Deletion
Base Sequence, Protein Stability, Science, Escherichia coli Proteins, Q, Host Factor 1 Protein, Models, Biological, Article, GTP Pyrophosphokinase, Protein Subunits, RNA, Bacterial, Amino Acid Substitution, Escherichia coli, RNA, Small Untranslated, Protein Multimerization, Protein Structure, Quaternary, Protein Binding, Sequence Deletion
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