Literature DB >> 14616075

RecA-dependent recovery of arrested DNA replication forks.

Justin Courcelle1, Philip C Hanawalt.   

Abstract

DNA damage encountered during the cellular process of chromosomal replication can disrupt the replication machinery and result in mutagenesis or lethality. The RecA protein of Escherichia coli is essential for survival in this situation: It maintains the integrity of the arrested replication fork and signals the upregulation of over 40 gene products, of which most are required to restore the genomic template and to facilitate the resumption of processive replication. Although RecA was originally discovered as a gene product that was required to change the genetic information during sexual cell cycles, over three decades of research have revealed that it is also the key enzyme required to maintain the genetic information when DNA damage is encountered during replication in asexual cell cycles. In this review, we examine the significant experimental approaches that have led to our current understanding of the RecA-mediated processes that restore replication following encounters with DNA damage.

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Year:  2003        PMID: 14616075     DOI: 10.1146/annurev.genet.37.110801.142616

Source DB:  PubMed          Journal:  Annu Rev Genet        ISSN: 0066-4197            Impact factor:   16.830


  83 in total

Review 1.  Multiple pathways process stalled replication forks.

Authors:  Bénédicte Michel; Gianfranco Grompone; Maria-Jose Florès; Vladimir Bidnenko
Journal:  Proc Natl Acad Sci U S A       Date:  2004-08-24       Impact factor: 11.205

2.  Replication forks stalled at ultraviolet lesions are rescued via RecA and RuvABC protein-catalyzed disintegration in Escherichia coli.

Authors:  Sharik R Khan; Andrei Kuzminov
Journal:  J Biol Chem       Date:  2011-12-21       Impact factor: 5.157

3.  Interplay of DNA repair, homologous recombination, and DNA polymerases in resistance to the DNA damaging agent 4-nitroquinoline-1-oxide in Escherichia coli.

Authors:  Ashley B Williams; Kyle M Hetrick; Patricia L Foster
Journal:  DNA Repair (Amst)       Date:  2010-08-19

4.  Rad51 recombinase prevents Mre11 nuclease-dependent degradation and excessive PrimPol-mediated elongation of nascent DNA after UV irradiation.

Authors:  María Belén Vallerga; Sabrina F Mansilla; María Belén Federico; Agustina P Bertolin; Vanesa Gottifredi
Journal:  Proc Natl Acad Sci U S A       Date:  2015-11-16       Impact factor: 11.205

5.  Recruitment of Bacillus subtilis RecN to DNA double-strand breaks in the absence of DNA end processing.

Authors:  Humberto Sanchez; Dawit Kidane; M Castillo Cozar; Peter L Graumann; Juan C Alonso
Journal:  J Bacteriol       Date:  2006-01       Impact factor: 3.490

6.  Transcription regulatory elements are punctuation marks for DNA replication.

Authors:  Ekaterina V Mirkin; Daniel Castro Roa; Evgeny Nudler; Sergei M Mirkin
Journal:  Proc Natl Acad Sci U S A       Date:  2006-05-02       Impact factor: 11.205

7.  Replication fork progression is impaired by transcription in hyperrecombinant yeast cells lacking a functional THO complex.

Authors:  Ralf E Wellinger; Félix Prado; Andrés Aguilera
Journal:  Mol Cell Biol       Date:  2006-04       Impact factor: 4.272

8.  Structural conservation of RecF and Rad50: implications for DNA recognition and RecF function.

Authors:  Olga Koroleva; Nodar Makharashvili; Charmain T Courcelle; Justin Courcelle; Sergey Korolev
Journal:  EMBO J       Date:  2007-01-25       Impact factor: 11.598

Review 9.  Chlamydomonas reinhardtii: a convenient model system for the study of DNA repair in photoautotrophic eukaryotes.

Authors:  Daniel Vlcek; Andrea Sevcovicová; Barbara Sviezená; Eliska Gálová; Eva Miadoková
Journal:  Curr Genet       Date:  2007-11-09       Impact factor: 3.886

10.  Chromatin organization and radio resistance in the bacterium Gemmata obscuriglobus.

Authors:  Arnon Lieber; Andrew Leis; Ariel Kushmaro; Abraham Minsky; Ohad Medalia
Journal:  J Bacteriol       Date:  2008-12-12       Impact factor: 3.490

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