Literature DB >> 7984091

When replication forks stop.

H Bierne1, B Michel.   

Abstract

DNA synthesis is an accurate and very processive phenomenon, yet chromosome replication does not proceed at a constant rate and progression of the replication fork can be impeded. Several structural and functional features of the template can modulate the rate of progress of the replication fork. These include DNA secondary structures, DNA damage and occupied protein-binding sites. In addition, prokaryotes contain sites where replication is specifically arrested. DNA regions at which the replication machinery is blocked or transiently slowed could be particularly susceptible to genome rearrangements. Illegitimate recombination, a ubiquitous phenomenon which may have dramatic consequences, occurs by a variety of mechanisms. The observation that some rearrangements might be facilitated by a pause in replication could provide a clue in elucidating these processes. In support of this, some homologous and illegitimate recombination events have already been correlated with replication pauses or arrest sites.

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Year:  1994        PMID: 7984091     DOI: 10.1111/j.1365-2958.1994.tb00398.x

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


  45 in total

1.  Sister chromatid exchanges are mediated by homologous recombination in vertebrate cells.

Authors:  E Sonoda; M S Sasaki; C Morrison; Y Yamaguchi-Iwai; M Takata; S Takeda
Journal:  Mol Cell Biol       Date:  1999-07       Impact factor: 4.272

2.  Visualisation of plasmid replication intermediates containing reversed forks.

Authors:  E Viguera; P Hernández; D B Krimer; R Lurz; J B Schvartzman
Journal:  Nucleic Acids Res       Date:  2000-01-15       Impact factor: 16.971

3.  Recombination enhancement by replication (RER) in Rhizobium etli.

Authors:  E Valencia-Morales; D Romero
Journal:  Genetics       Date:  2000-03       Impact factor: 4.562

4.  An antitumor drug-induced topoisomerase cleavage complex blocks a bacteriophage T4 replication fork in vivo.

Authors:  G Hong; K N Kreuzer
Journal:  Mol Cell Biol       Date:  2000-01       Impact factor: 4.272

5.  Visualization of repair of double-strand breaks in the bacteriophage T7 genome without normal DNA replication.

Authors:  Y T Lai; W Masker
Journal:  J Bacteriol       Date:  2000-01       Impact factor: 3.490

6.  Tandem repeat recombination induced by replication fork defects in Escherichia coli requires a novel factor, RadC.

Authors:  C J Saveson; S T Lovett
Journal:  Genetics       Date:  1999-05       Impact factor: 4.562

7.  Replication by a single DNA polymerase of a stretched single-stranded DNA.

Authors:  B Maier; D Bensimon; V Croquette
Journal:  Proc Natl Acad Sci U S A       Date:  2000-10-24       Impact factor: 11.205

Review 8.  Rescue of arrested replication forks by homologous recombination.

Authors:  B Michel; M J Flores; E Viguera; G Grompone; M Seigneur; V Bidnenko
Journal:  Proc Natl Acad Sci U S A       Date:  2001-07-17       Impact factor: 11.205

Review 9.  Historical overview: searching for replication help in all of the rec places.

Authors:  M M Cox
Journal:  Proc Natl Acad Sci U S A       Date:  2001-07-17       Impact factor: 11.205

10.  Homologous recombination is essential for RAD51 up-regulation in Saccharomyces cerevisiae following DNA crosslinking damage.

Authors:  Yuval Cohen; Michele Dardalhon; Dietrich Averbeck
Journal:  Nucleic Acids Res       Date:  2002-03-01       Impact factor: 16.971

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