E. coli DNA associated with isolated Hfq interacts with Hfq's distal surface and C-terminal domain

• Published in: Biochimica et biophysica acta Vol. 1799; no. 8; pp. 588 - 596
• Main Authors: Updegrove, Taylor B., Correia, John J., Galletto, Roberto, Bujalowski, Wlodzimierz, Wartell, Roger M.
• Format: Journal Article
• Language: English
• Published: Netherlands Elsevier B.V 01.08.2010
• Subjects: DNA, Bacterial - genetics; DNA, Bacterial - metabolism; Electrophoretic Mobility Shift Assay; Escherichia coli; Escherichia coli - genetics; Escherichia coli - metabolism; Escherichia coli Proteins - chemistry; Escherichia coli Proteins - genetics; Escherichia coli Proteins - metabolism; Hfq protein; Hfq-DNA binding; Host Factor 1 Protein - chemistry; Host Factor 1 Protein - genetics; Host Factor 1 Protein - metabolism; Models, Molecular; Mutation - genetics; Protein Conformation; Protein Structure, Tertiary; Ultracentrifugation; MWCO; Hfq protein; FAM; Hfq-DNA binding; nt; sRNA; PAGE; bp
• ISSN: 1874-9399; 0006-3002; 1876-4320
• DOI: 10.1016/j.bbagrm.2010.06.007

The RNA-binding protein Hfq has been studied extensively for its function as a modulator of gene expression at the post-transcriptional level. While most Hfq studies have focused on the protein's interaction with sRNAs and mRNAs, Hfq binding to DNA has been observed but is less explored. During the isolation of Hfq from E scherichia coli, we found genomic DNA fragments associated with the protein after multiple steps of purification. Sequences of 41 amplified segments from the DNA fragments associated with Hfq were determined. A large fraction of the DNA segments were predicted to have significant helical axis curvature and were from genes associated with membrane proteins, characteristics unexpected for non-specific binding. Analysis by analytical ultracentrifugation indicated that rA 18 binding to Hfq disrupts Hfq-DNA interactions. The latter observation suggests Hfq binding to DNA involves its distal surface. This was supported by a gel mobility shift assay that showed single amino acid mutations on the distal surface of Hfq inhibited Hfq binding to duplex DNA, while six of seven mutations on the proximal surface and outer circumference of the hexamer did not prevent Hfq binding. Two mutated Hfq which have portions of their C-terminal domain removed also failed to bind to DNA. The apparent K d for binding wild type Hfq to several duplex DNA was estimated from a gel mobility shift assay to be ~ 400 nM.