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 - 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.
UR - https://www.scopus.com/pages/publications/85046889001
UR - https://www.scopus.com/pages/publications/85046889001#tab=citedBy
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 -