Mutations Affecting Potassium Import Restore the Viability of the Escherichia coli DNA Polymerase III holD Mutant

Adeline Durand1, Anurag Kumar Sinha1, Cloelia Dard-Dascot2

  • 1Genome biology department, Institute for Integrative Biology of the Cell (I2BC), CEA, CNRS, Université Paris-Sud, Université Paris-Saclay, 91198 Gif-sur-Yvette, France.

Plos Genetics
|June 10, 2016
PubMed

Insights

Mutants lacking the HolD subunit of DNA Polymerase III holoenzyme (Pol III HE) are rescued by decreasing potassium import. This finding reveals a novel mechanism for stabilizing essential protein-DNA interactions.

Area of Science:

  • Molecular Biology
  • Genetics
  • Biochemistry

Background:

  • The HolD (ψ) subunit is essential for the viability of Escherichia coli DNA Polymerase III holoenzyme (Pol III HE).
  • Mutants lacking HolD exhibit poor viability, but suppressor mutations can restore growth.

Purpose of the Study:

  • To identify and characterize suppressor mutations that restore viability to ΔholD mutants.
  • To elucidate the mechanism by which these suppressors rescue the ΔholD phenotype.

Main Methods:

  • Isolation and characterization of spontaneous suppressor mutations in ΔholD Escherichia coli mutants.
  • Genetic analysis of suppressor mutations in trkA and trkE genes, involved in potassium import.
  • Assessment of mutant viability under varying potassium concentrations and in combination with other suppressor mutations (lexAind, ssb).

Main Results:

  • Two suppressor mutations were identified in the trkA and trkE potassium import genes.
  • ΔholD trk mutants show abolished viability at extreme potassium concentrations but are rescued by decreased potassium import.
  • The suppressive effect of trk inactivation is additive with lexAind and ssb mutations, suggesting an SOS-independent mechanism.
  • The trkA mutation allows HolD-less Pol III HE to tolerate increased levels of the DinB polymerase.

Conclusions:

  • Decreased intracellular potassium concentration rescues the essential protein-DNA interaction defect in ΔholD mutants.
  • This rescue is likely mediated by increased electrostatic interactions or altered SSB binding, stabilizing the HolD-less Pol III HE on DNA.
  • This study highlights the critical role of potassium import in maintaining essential protein-DNA interactions in vivo.

Related Concept Videos

Translesion DNA Polymerases02:10

Translesion DNA Polymerases

Translesion (TLS) polymerases rescue stalled DNA polymerases at sites of damaged bases by replacing the replicative polymerase and installing a nucleotide across the damaged site. Doing so, TLS allows additional time for the cell to repair the damage before resuming regular DNA replication.
TLS polymerases are found in all three domains of life - archaea, bacteria, and eukaryotes. Of the different classes of TLS polymerases, members of the Y family are fitted with specialized structures that...
11.6K
Mismatch Repair01:20

Mismatch Repair

Organisms are capable of detecting and fixing nucleotide mismatches that occur during DNA replication. This sophisticated process requires identifying the new strand and replacing the erroneous bases with correct nucleotides. Mismatch repair is coordinated by many proteins in both prokaryotes and eukaryotes.
The Mutator Protein Family Plays a Key Role in DNA Mismatch Repair
The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...
6.9K
Mismatch Repair01:36

Mismatch Repair

Overview
44.8K
Proofreading01:31

Proofreading

Synthesis of new DNA molecules is carried out by the enzyme DNA polymerase, which adds nucleotides on the daughter strand complementary to the template DNA strand. DNA polymerase has a higher affinity to add the correct base and ensures fidelity during DNA replication. Furthermore,  it exhibits proofreading activity during replication, using an exonuclease domain that cuts off incorrect nucleotides from the nascent DNA strand.
Errors During Replication are Corrected by the DNA Polymerase...
9.7K
Proofreading01:43

Proofreading

Overview
61.9K
Genome Copying Errors02:46

Genome Copying Errors

DNA replication is a well-evolved process that copies millions of base pairs with high fidelity during each cell division. Occasionally a wrong base or a long stretch of wrong bases may get added to the daughter strands. If the errors are left unchecked, cells might accumulate several mutations that might endanger their  survival. Therefore, the copying errors are checked and repaired at three levels.
5.4K