A deoxynucleoside triphosphate triphosphohydrolase promotes cell cycle progression in <i>Caulobacter crescentus</i>

Intracellular pools of deoxynucleoside triphosphates (dNTPs) are strictly maintained throughout the cell cycle to ensure accurate and efficient DNA replication. DNA synthesis requires an abundance of dNTPs, but elevated dNTP concentrations in nonreplicating cells delay entry into S phase. Enzymes known as deoxyguanosine triphosphate triphosphohydrolases (Dgts) hydrolyze dNTPs into deoxynucleosides and triphosphates, and we propose that Dgts restrict dNTP concentrations to promote the G1 to S phase transition. We characterized a Dgt from the bacterium <i>Caulobacter crescentus</i> termed <i>flagellar signaling suppressor C</i> (<i>fssC</i>) to clarify the role of Dgts in cell cycle regulation. Deleting <i>fssC</i> increases dNTP levels and extends the G1 phase of the cell cycle through a mechanism independent of the response regulator CtrA. Segregation and duplication of the chromosomal origin of replication (<i>oriC</i>) are delayed in ∆<i>fssC</i>, but the rate of replication elongation is unchanged. We conclude that dNTP hydrolysis by FssC promotes the initiation of DNA replication. This work further establishes Dgts as important regulators of the G1 to S phase transition, and the high conservation of Dgts across all domains of life implies that Dgt-dependent cell cycle control may be widespread in many organisms.IMPORTANCECells must faithfully replicate their genetic material in order to proliferate. Studying the regulatory pathways that determine when a cell initiates DNA replication is important for understanding fundamental biological processes, and it can also improve the strategies used to treat diseases that affect the cell cycle. Here, we identify a nucleotide signaling pathway that influences when cells begin DNA replication. We show that this pathway promotes the transition from the G1 to the S phase of the cell cycle in the bacterium <i>Caulobacter crescentus</i> and propose that this pathway is prevalent in all domains of life.

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Publication Details

Journal
Journal of Bacteriology
Published
2025-06-02
DOI
https://doi.org/10.1128/jb.00145-25
Citations
2
Primary Topic
Amino Acid Enzymes and Metabolism
Type
article
Field-Weighted Citation Impact
2.22

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article

A deoxynucleoside triphosphate triphosphohydrolase promotes cell cycle progression in Caulobacter crescentus

David Stevenson, Katarzyna A. Gromek, Daniel Amador‐Noguez, David M. Hershey et al.
2 citations
Journal of Bacteriology
Amino Acid Enzymes and Metabolism
2.22
article

A deoxynucleoside triphosphate triphosphohydrolase promotes cell cycle progression in Caulobacter crescentus

David Stevenson, Katarzyna A. Gromek, Daniel Amador‐Noguez, David M. Hershey, Chandler N. Hellenbrand
article en
2 citations

Abstract

Intracellular pools of deoxynucleoside triphosphates (dNTPs) are strictly maintained throughout the cell cycle to ensure accurate and efficient DNA replication. DNA synthesis requires an abundance of dNTPs, but elevated dNTP concentrations in nonreplicating cells delay entry into S phase. Enzymes known as deoxyguanosine triphosphate triphosphohydrolases (Dgts) hydrolyze dNTPs into deoxynucleosides and triphosphates, and we propose that Dgts restrict dNTP concentrations to promote the G1 to S phase transition. We characterized a Dgt from the bacterium <i>Caulobacter crescentus</i> termed <i>flagellar signaling suppressor C</i> (<i>fssC</i>) to clarify the role of Dgts in cell cycle regulation. Deleting <i>fssC</i> increases dNTP levels and extends the G1 phase of the cell cycle through a mechanism independent of the response regulator CtrA. Segregation and duplication of the chromosomal origin of replication (<i>oriC</i>) are delayed in ∆<i>fssC</i>, but the rate of replication elongation is unchanged. We conclude that dNTP hydrolysis by FssC promotes the initiation of DNA replication. This work further establishes Dgts as important regulators of the G1 to S phase transition, and the high conservation of Dgts across all domains of life implies that Dgt-dependent cell cycle control may be widespread in many organisms.IMPORTANCECells must faithfully replicate their genetic material in order to proliferate. Studying the regulatory pathways that determine when a cell initiates DNA replication is important for understanding fundamental biological processes, and it can also improve the strategies used to treat diseases that affect the cell cycle. Here, we identify a nucleotide signaling pathway that influences when cells begin DNA replication. We show that this pathway promotes the transition from the G1 to the S phase of the cell cycle in the bacterium <i>Caulobacter crescentus</i> and propose that this pathway is prevalent in all domains of life.

Journal of BacteriologyVol. 207(6)
University of Wisconsin–Madison (US)
National Institutes of Health, National Science Foundation of Sri Lanka
Life in Land
Openalex Percentile: Top 13%
Amino Acid Enzymes and Metabolism
2.22
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