Literature DB >> 16936035

sbcB15 And DeltasbcB mutations activate two types of recf recombination pathways in Escherichia coli.

Ksenija Zahradka1, Sanela Simic, Maja Buljubasic, Mirjana Petranovic, Damir Dermic, Davor Zahradka.   

Abstract

Escherichia coli cells with mutations in recBC genes are defective for the main RecBCD pathway of recombination and have severe reductions in conjugational and transductional recombination, as well as in recombinational repair of double-stranded DNA breaks. This phenotype can be corrected by suppressor mutations in sbcB and sbcC(D) genes, which activate an alternative RecF pathway of recombination. It was previously suggested that sbcB15 and DeltasbcB mutations, both of which inactivate exonuclease I, are equally efficient in suppressing the recBC phenotype. In the present work we reexamined the effects of sbcB15 and DeltasbcB mutations on DNA repair after UV and gamma irradiation, on conjugational recombination, and on the viability of recBC (sbcC) cells. We found that the sbcB15 mutation is a stronger recBC suppressor than DeltasbcB, suggesting that some unspecified activity of the mutant SbcB15 protein may be favorable for recombination in the RecF pathway. We also showed that the xonA2 mutation, a member of another class of ExoI mutations, had the same effect on recombination as DeltasbcB, suggesting that it is an sbcB null mutation. In addition, we demonstrated that recombination in a recBC sbcB15 sbcC mutant is less affected by recF and recQ mutations than recombination in recBC DeltasbcB sbcC and recBC xonA2 sbcC strains is, indicating that SbcB15 alleviates the requirement for the RecFOR complex and RecQ helicase in recombination processes. Our results suggest that two types of sbcB-sensitive RecF pathways can be distinguished in E. coli, one that is activated by the sbcB15 mutation and one that is activated by sbcB null mutations. Possible roles of SbcB15 in recombination reactions in the RecF pathway are discussed.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16936035      PMCID: PMC1636276          DOI: 10.1128/JB.00613-06

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  39 in total

1.  recD sbcB sbcD mutants are deficient in recombinational repair of UV lesions by RecBC.

Authors:  M Seigneur; S D Ehrlich; B Michel
Journal:  J Bacteriol       Date:  1999-10       Impact factor: 3.490

2.  Facilitated loading of RecA protein is essential to recombination by RecBCD enzyme.

Authors:  D A Arnold; S C Kowalczykowski
Journal:  J Biol Chem       Date:  2000-04-21       Impact factor: 5.157

3.  RecFOR proteins load RecA protein onto gapped DNA to accelerate DNA strand exchange: a universal step of recombinational repair.

Authors:  Katsumi Morimatsu; Stephen C Kowalczykowski
Journal:  Mol Cell       Date:  2003-05       Impact factor: 17.970

4.  The RuvABC resolvase is indispensable for recombinational repair in sbcB15 mutants of Escherichia coli.

Authors:  Davor Zahradka; Ksenija Zahradka; Mirjana Petranović; Damir Dermić; Krunoslav Brcić-Kostić
Journal:  J Bacteriol       Date:  2002-08       Impact factor: 3.490

5.  Genetic recombination in Escherichia coli: the role of exonuclease I.

Authors:  S R Kushner; H Nagaishi; A Templin; A J Clark
Journal:  Proc Natl Acad Sci U S A       Date:  1971-04       Impact factor: 11.205

6.  Recombination deficient mutants of Escherichia coli K12 that map between thy A and argA.

Authors:  P T Emmerson
Journal:  Genetics       Date:  1968-09       Impact factor: 4.562

Review 7.  Recombinational repair of DNA damage in Escherichia coli and bacteriophage lambda.

Authors:  A Kuzminov
Journal:  Microbiol Mol Biol Rev       Date:  1999-12       Impact factor: 11.056

8.  Extent of host deletions associated with bacteriophage P2-mediated eduction.

Authors:  M G Sunshine; B Kelly
Journal:  J Bacteriol       Date:  1971-11       Impact factor: 3.490

9.  The RecD subunit of the Escherichia coli RecBCD enzyme inhibits RecA loading, homologous recombination, and DNA repair.

Authors:  S K Amundsen; A F Taylor; G R Smith
Journal:  Proc Natl Acad Sci U S A       Date:  2000-06-20       Impact factor: 11.205

10.  Indirect suppression of recB and recC mutations by exonuclease I deficiency.

Authors:  S R Kushner; H Nagaishi; A J Clark
Journal:  Proc Natl Acad Sci U S A       Date:  1972-06       Impact factor: 11.205

View more
  4 in total

1.  Effects of single-strand DNases ExoI, RecJ, ExoVII, and SbcCD on homologous recombination of recBCD+ strains of Escherichia coli and roles of SbcB15 and XonA2 ExoI mutant enzymes.

Authors:  Brigitte Thoms; Inka Borchers; Wilfried Wackernagel
Journal:  J Bacteriol       Date:  2007-10-26       Impact factor: 3.490

2.  Roles of ExoI and SbcCD nucleases in "reckless" DNA degradation in recA mutants of Escherichia coli.

Authors:  Ksenija Zahradka; Maja Buljubasić; Mirjana Petranović; Davor Zahradka
Journal:  J Bacteriol       Date:  2008-12-12       Impact factor: 3.490

3.  Identification of two conserved aspartic acid residues required for DNA digestion by a novel thermophilic Exonuclease VII in Thermotoga maritima.

Authors:  Andres A Larrea; Ilene M Pedroso; Arun Malhotra; Richard S Myers
Journal:  Nucleic Acids Res       Date:  2008-09-23       Impact factor: 16.971

Review 4.  The Roles of Bacterial DNA Double-Strand Break Repair Proteins in Chromosomal DNA Replication.

Authors:  Anurag Kumar Sinha; Christophe Possoz; David R F Leach
Journal:  FEMS Microbiol Rev       Date:  2020-05-01       Impact factor: 16.408

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.