Literature DB >> 34389317

The Alarmone (p)ppGpp Regulates Primer Extension by Bacterial Primase.

Christina N Giramma1, McKenna B DeFoer1, Jue D Wang2.   

Abstract

Primase is an essential component of the DNA replication machinery, responsible for synthesizing RNA primers that initiate leading and lagging strand DNA synthesis. Bacterial primase activity can be regulated by the starvation-inducible nucleotide (p)ppGpp. This regulation contributes to a timely inhibition of DNA replication upon amino acid starvation in the Gram-positive bacterium Bacillus subtilis. Here, we characterize the effect of (p)ppGpp on B. subtilis DnaG primase activity in vitro. Using a single-nucleotide resolution primase assay, we dissected the effect of ppGpp on the initiation, extension, and fidelity of B. subtilis primase. We found that ppGpp has a mild effect on initiation, but strongly inhibits primer extension and reduces primase processivity, promoting termination of primer extension. High (p)ppGpp concentration, together with low GTP concentration, additively inhibit primase activity. This explains the strong inhibition of replication elongation during starvation which induces high levels of (p)ppGpp and depletion of GTP in B. subtilis. Finally, we found that lowering GTP concentration results in mismatches in primer base pairing that allow priming readthrough, and that ppGpp reduces readthrough to protect priming fidelity. These results highlight the importance of (p)ppGpp in protecting replisome integrity and genome stability in fluctuating nucleotide concentrations upon onset of environmental stress.
Copyright © 2021 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  (p)ppGpp; bacterial primase; genome stability; regulation of DNA replication; the stringent response

Mesh:

Substances:

Year:  2021        PMID: 34389317      PMCID: PMC8453095          DOI: 10.1016/j.jmb.2021.167189

Source DB:  PubMed          Journal:  J Mol Biol        ISSN: 0022-2836            Impact factor:   6.151


  61 in total

1.  Nutritional control of elongation of DNA replication by (p)ppGpp.

Authors:  Jue D Wang; Glenn M Sanders; Alan D Grossman
Journal:  Cell       Date:  2007-03-09       Impact factor: 41.582

2.  Factor-independent activation of Escherichia coli rRNA transcription. I. Kinetic analysis of the roles of the upstream activator region and supercoiling on transcription of the rrnB P1 promoter in vitro.

Authors:  S Leirmo; R L Gourse
Journal:  J Mol Biol       Date:  1991-08-05       Impact factor: 5.469

3.  Intramolecular regulation of the opposing (p)ppGpp catalytic activities of Rel(Seq), the Rel/Spo enzyme from Streptococcus equisimilis.

Authors:  Undine Mechold; Helen Murphy; Larissa Brown; Michael Cashel
Journal:  J Bacteriol       Date:  2002-06       Impact factor: 3.490

4.  Interaction of Escherichia coli primase with a phage G4ori(c)-E. coli SSB complex.

Authors:  W Sun; G N Godson
Journal:  J Bacteriol       Date:  1996-12       Impact factor: 3.490

5.  Binding of Escherichia coli RNA polymerase to T7 DNA. Displacement of holoenzyme from promoter complexes by heparin.

Authors:  S R Pfeffer; S J Stahl; M J Chamberlin
Journal:  J Biol Chem       Date:  1977-08-10       Impact factor: 5.157

6.  ppGpp inhibits the activity of Escherichia coli DnaG primase.

Authors:  Monika Maciag; Maja Kochanowska; Robert Lyzeń; Grzegorz Wegrzyn; Agnieszka Szalewska-Pałasz
Journal:  Plasmid       Date:  2009-11-27       Impact factor: 3.466

Review 7.  Mechanism and evolution of DNA primases.

Authors:  Robert D Kuchta; Gudrun Stengel
Journal:  Biochim Biophys Acta       Date:  2009-06-21

Review 8.  Regulation of bacterial priming and daughter strand synthesis through helicase-primase interactions.

Authors:  Jacob E Corn; James M Berger
Journal:  Nucleic Acids Res       Date:  2006-08-25       Impact factor: 16.971

9.  Different effects of ppGpp on Escherichia coli DNA replication in vivo and in vitro.

Authors:  Monika Maciąg-Dorszyńska; Agnieszka Szalewska-Pałasz; Grzegorz Węgrzyn
Journal:  FEBS Open Bio       Date:  2013-03-06       Impact factor: 2.693

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.