| Literature DB >> 26373314 |
Daniel J Schu1, Aixia Zhang2, Susan Gottesman3, Gisela Storz4.
Abstract
Many bacteria use small RNAs (sRNAs) and the RNA chaperone Hfq to regulate mRNA stability and translation. Hfq, a ring-shaped homohexamer, has multiple faces that can bind both sRNAs and their mRNA targets. We find that Hfq has at least two distinct ways in which it interacts with sRNAs; these different binding properties have strong effects on the stability of the sRNA in vivo and the sequence requirements of regulated mRNAs. Class I sRNAs depend on proximal and rim Hfq sites for stability and turn over rapidly. Class II sRNAs are more stable and depend on the proximal and distal Hfq sites for stabilization. Using deletions and chimeras, we find that while Class I sRNAs regulate mRNA targets with previously defined ARN repeats, Class II sRNAs regulate mRNAs carrying UA-rich rim-binding sites. We discuss how these different binding modes may correlate with different roles in the cell, with Class I sRNAs acting as emergency responders and Class II sRNAs acting as silencers. Published 2015. This article is a U.S. Government work and is in the public domain in the USA.Entities:
Keywords: ChiX; Hfq; MgrR; RyhB
Mesh:
Substances:
Year: 2015 PMID: 26373314 PMCID: PMC4609186 DOI: 10.15252/embj.201591569
Source DB: PubMed Journal: EMBO J ISSN: 0261-4189 Impact factor: 11.598