Literature DB >> 14507374

Lethality of bypass polymerases in Escherichia coli cells with a defective clamp loader complex of DNA polymerase III.

Enrique Viguera1, Mirjana Petranovic, Davor Zahradka, Karine Germain, Dusko S Ehrlich, Bénédicte Michel.   

Abstract

Escherichia coli DNA polymerase III (Pol III) is one of the best studied replicative DNA polymerases. Here we report the properties of an E. coli mutant that lacks one of the subunits of the Pol III clamp loader complex, Psi (psi), as a result of the complete inactivation of the holD gene. We show that, in this mutant, chronic induction of the SOS response in a RecFOR-dependent way leads to lethality at high temperature. The SOS-induced proteins that are lethal in the holD mutant are the specialized DNA polymerases Pol II and Pol IV, combined with the division inhibitor SfiA. Prevention of SOS induction or inactivation of Pol II, Pol IV and SfiA encoding genes allows growth of the holD mutant, although at a reduced rate compared to a wild-type cell. In contrast, the SOS-induced Pol V DNA polymerase does not participate to the lethality of the holD mutant. We conclude that: (i) Psi is essential for efficient replication of the E. coli chromosome; (ii) SOS-induction of specialized DNA polymerases can be lethal in cells in which the replicative polymerase is defective, and (iii) specialized DNA polymerases differ in respect to their access to inactivated replication forks.

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Year:  2003        PMID: 14507374     DOI: 10.1046/j.1365-2958.2003.03658.x

Source DB:  PubMed          Journal:  Mol Microbiol        ISSN: 0950-382X            Impact factor:   3.501


  17 in total

1.  Nucleotide excision repair or polymerase V-mediated lesion bypass can act to restore UV-arrested replication forks in Escherichia coli.

Authors:  Charmain T Courcelle; Jerilyn J Belle; Justin Courcelle
Journal:  J Bacteriol       Date:  2005-10       Impact factor: 3.490

2.  Structure of the SSB-DNA polymerase III interface and its role in DNA replication.

Authors:  Aimee H Marceau; Soon Bahng; Shawn C Massoni; Nicholas P George; Steven J Sandler; Kenneth J Marians; James L Keck
Journal:  EMBO J       Date:  2011-08-19       Impact factor: 11.598

3.  Roles of the Escherichia coli RecA protein and the global SOS response in effecting DNA polymerase selection in vivo.

Authors:  Robert W Maul; Mark D Sutton
Journal:  J Bacteriol       Date:  2005-11       Impact factor: 3.490

4.  Expression of canonical SOS genes is not under LexA repression in Bdellovibrio bacteriovorus.

Authors:  Susana Campoy; Noelia Salvador; Pilar Cortés; Ivan Erill; Jordi Barbé
Journal:  J Bacteriol       Date:  2005-08       Impact factor: 3.490

5.  The Mutant βE202K Sliding Clamp Protein Impairs DNA Polymerase III Replication Activity.

Authors:  Caleb Homiski; Michelle K Scotland; Vignesh M P Babu; Sundari Chodavarapu; Robert W Maul; Jon M Kaguni; Mark D Sutton
Journal:  J Bacteriol       Date:  2021-09-20       Impact factor: 3.490

6.  Interplay between replication and recombination in Escherichia coli: impact of the alternative DNA polymerases.

Authors:  Stéphane Delmas; Ivan Matic
Journal:  Proc Natl Acad Sci U S A       Date:  2006-03-13       Impact factor: 11.205

Review 7.  Coordinating DNA polymerase traffic during high and low fidelity synthesis.

Authors:  Mark D Sutton
Journal:  Biochim Biophys Acta       Date:  2009-06-21

Review 8.  DNA Replication in Mycobacterium tuberculosis.

Authors:  Zanele Ditse; Meindert H Lamers; Digby F Warner
Journal:  Microbiol Spectr       Date:  2017-03

9.  Alternative complexes formed by the Escherichia coli clamp loader accessory protein HolC (x) with replication protein HolD (ψ) and repair protein YoaA.

Authors:  Vincent A Sutera; Savannah J Weeks; Elizabeth E Dudenhausen; Helen B Rappe Baggett; McKay C Shaw; Kirsten A Brand; David J Glass; Linda B Bloom; Susan T Lovett
Journal:  DNA Repair (Amst)       Date:  2021-02-02

10.  ssb gene duplication restores the viability of ΔholC and ΔholD Escherichia coli mutants.

Authors:  Stéphane Duigou; Maud Silvain; Enrique Viguera; Bénédicte Michel
Journal:  PLoS Genet       Date:  2014-10-16       Impact factor: 5.917

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