TY - JOUR
T1 - RNase I regulates Escherichia coli 20,30-cyclic nucleotide monophosphate levels and biofilm formation
AU - Fontaine, Benjamin M.
AU - Martin, Kevin S.
AU - Garcia-Rodriguez, Jennifer M.
AU - Jung, Claire
AU - Briggs, Laura
AU - Southwell, Jessica E.
AU - Jia, Xin
AU - Weinert, Emily E.
N1 - Funding Information:
This work was supported by Emory University. The present study was supported, in part, by the Emory Integrated Genomics Core (EIGC), which is subsidized by the Emory University School of Medicine and is one of the Emory Integrated Core Facilities. Additional support for the EIGC was provided by the National Center for Advancing Translational Sciences of the National Institutes of Health under Award Number UL1TR000454.
Publisher Copyright:
© 2018 The Author(s).
PY - 2018/4/30
Y1 - 2018/4/30
N2 - Regulation of nucleotide and nucleoside concentrations is critical for faithful DNA replication, transcription, and translation in all organisms, and has been linked to bacterial biofilm formation. Unusual 20,30-cyclic nucleotide monophosphates (20,30-cNMPs) recently were quantified in mammalian systems, and previous reports have linked these nucleotides to cellular stress and damage in eukaryotes, suggesting an intriguing connection with nucleotide/nucleoside pools and/or cyclic nucleotide signaling. This work reports the first quantification of 20,30-cNMPs in Escherichia coli and demonstrates that 20,30-cNMP levels in E. coli are generated specifically from RNase I-catalyzed RNA degradation, presumably as part of a previously unidentified nucleotide salvage pathway. Furthermore, RNase I and 20,30-cNMP levels are demonstrated to play an important role in controlling biofilm formation. This work identifies a physiological role for cytoplasmic RNase I and constitutes the first progress toward elucidating the biological functions of bacterial 20,30-cNMPs.
AB - Regulation of nucleotide and nucleoside concentrations is critical for faithful DNA replication, transcription, and translation in all organisms, and has been linked to bacterial biofilm formation. Unusual 20,30-cyclic nucleotide monophosphates (20,30-cNMPs) recently were quantified in mammalian systems, and previous reports have linked these nucleotides to cellular stress and damage in eukaryotes, suggesting an intriguing connection with nucleotide/nucleoside pools and/or cyclic nucleotide signaling. This work reports the first quantification of 20,30-cNMPs in Escherichia coli and demonstrates that 20,30-cNMP levels in E. coli are generated specifically from RNase I-catalyzed RNA degradation, presumably as part of a previously unidentified nucleotide salvage pathway. Furthermore, RNase I and 20,30-cNMP levels are demonstrated to play an important role in controlling biofilm formation. This work identifies a physiological role for cytoplasmic RNase I and constitutes the first progress toward elucidating the biological functions of bacterial 20,30-cNMPs.
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U2 - 10.1042/BCJ20170906
DO - 10.1042/BCJ20170906
M3 - Article
C2 - 29555843
AN - SCOPUS:85046889001
SN - 0264-6021
VL - 475
SP - 1491
EP - 1506
JO - Biochemical Journal
JF - Biochemical Journal
IS - 8
ER -