Literature DB >> 10589843

RecQ and RecJ process blocked replication forks prior to the resumption of replication in UV-irradiated Escherichia coli.

J Courcelle1, P C Hanawalt.   

Abstract

The accurate recovery of replication following DNA damage and repair is critical for the maintenance of genomic integrity. In Escherichia coli, the recovery of replication following UV-induced DNA damage is dependent upon several proteins in the recF pathway, including RecF, RecO, and RecR. Two other recF pathway proteins, the RecQ helicase and the RecJ exonuclease, have been shown to affect the sites and frequencies at which illegitimate rearrangements occur following UV-induced DNA damage, suggesting that they also may function during the recovery of replication. We show here that RecQ and RecJ process the nascent DNA at blocked replication forks prior to the resumption of DNA synthesis. The processing involves selective degradation of the nascent lagging DNA strand and it requires both RecQ and RecJ. We suggest that this processing may serve to lengthen the substrate that can be recognized and stabilized by the RecA protein at the replication fork, thereby helping to ensure the accurate recovery of replication after the obstructing lesion has been repaired.

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Year:  1999        PMID: 10589843     DOI: 10.1007/s004380051116

Source DB:  PubMed          Journal:  Mol Gen Genet        ISSN: 0026-8925


  110 in total

1.  The Bloom's syndrome gene product promotes branch migration of holliday junctions.

Authors:  J K Karow; A Constantinou; J L Li; S C West; I D Hickson
Journal:  Proc Natl Acad Sci U S A       Date:  2000-06-06       Impact factor: 11.205

2.  Partial suppression of the fission yeast rqh1(-) phenotype by expression of a bacterial Holliday junction resolvase.

Authors:  C L Doe; J Dixon; F Osman; M C Whitby
Journal:  EMBO J       Date:  2000-06-01       Impact factor: 11.598

Review 3.  Participation of recombination proteins in rescue of arrested replication forks in UV-irradiated Escherichia coli need not involve recombination.

Authors:  J Courcelle; P C Hanawalt
Journal:  Proc Natl Acad Sci U S A       Date:  2001-07-17       Impact factor: 11.205

4.  Werner syndrome exonuclease catalyzes structure-dependent degradation of DNA.

Authors:  J C Shen; L A Loeb
Journal:  Nucleic Acids Res       Date:  2000-09-01       Impact factor: 16.971

5.  Translocation of E. coli RecQ helicase on single-stranded DNA.

Authors:  Behzad Rad; Stephen C Kowalczykowski
Journal:  Biochemistry       Date:  2012-03-21       Impact factor: 3.162

6.  Roles of RecJ, RecO, and RecR in RecET-mediated illegitimate recombination in Escherichia coli.

Authors:  Kouya Shiraishi; Katsuhiro Hanada; Yoichiro Iwakura; Hideo Ikeda
Journal:  J Bacteriol       Date:  2002-09       Impact factor: 3.490

7.  Domain mapping of Escherichia coli RecQ defines the roles of conserved N- and C-terminal regions in the RecQ family.

Authors:  Douglas A Bernstein; James L Keck
Journal:  Nucleic Acids Res       Date:  2003-06-01       Impact factor: 16.971

8.  RuvAB and RecG are not essential for the recovery of DNA synthesis following UV-induced DNA damage in Escherichia coli.

Authors:  Janet R Donaldson; Charmain T Courcelle; Justin Courcelle
Journal:  Genetics       Date:  2004-04       Impact factor: 4.562

9.  High-resolution structure of the E.coli RecQ helicase catalytic core.

Authors:  Douglas A Bernstein; Morgan C Zittel; James L Keck
Journal:  EMBO J       Date:  2003-10-01       Impact factor: 11.598

10.  The Neurospora crassa mus-19 gene is identical to the qde-3 gene, which encodes a RecQ homologue and is involved in recombination repair and postreplication repair.

Authors:  Akihiro Kato; Yufuko Akamatsu; Yoshiyuki Sakuraba; Hirokazu Inoue
Journal:  Curr Genet       Date:  2003-11-01       Impact factor: 3.886

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