
pmid: 15381101
The ring-shaped RNA chaperone Hfq has recently received much attention owing to its multiple roles in RNA metabolism. In this study we have performed a mutational analysis of the Escherichia coli hfq gene, and have studied the effects of amino acid substitutions at several positions in the Hfq protein as well as of C-terminal truncations on its role in phage Qbeta replication, in repression of a target mRNA, and on the stability of the small regulatory RNA DsrA. These functional studies provided insights into the interaction of Hfq with RNA and suggested a role for the C-terminus of Hfq in DsrA stability.
Allolevivirus, 106022 Mikrobiologie, RNA, Untranslated, Escherichia coli Proteins, Host Factor 1 Protein, Recombinant Proteins, Structure-Activity Relationship, Amino Acid Substitution, Escherichia coli, Mutagenesis, Site-Directed, 106022 Microbiology, RNA, RNA, Small Untranslated, Bacterial Outer Membrane Proteins, Molecular Chaperones
Allolevivirus, 106022 Mikrobiologie, RNA, Untranslated, Escherichia coli Proteins, Host Factor 1 Protein, Recombinant Proteins, Structure-Activity Relationship, Amino Acid Substitution, Escherichia coli, Mutagenesis, Site-Directed, 106022 Microbiology, RNA, RNA, Small Untranslated, Bacterial Outer Membrane Proteins, Molecular Chaperones
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