Literature DB >> 24951952

Replication forks reverse at high frequency upon replication stress in Physarum polycephalum.

Chrystelle Maric1, Marianne Bénard.   

Abstract

The addition of hydroxyurea after the onset of S phase allows replication to start and permits the successive detecting of replication-dependent joint DNA molecules and chicken foot structures in the synchronous nuclei of Physarum polycephalum. We find evidence for a very high frequency of reversed replication forks upon replication stress. The formation of these reversed forks is dependent on the presence of joint DNA molecules, the impediment of the replication fork progression by hydroxyurea, and likely on the propensity of some replication origins to reinitiate replication to counteract the action of this compound. As hydroxyurea treatment enables us to successively detect the appearance of joint DNA molecules and then of reversed replication forks, we propose that chicken foot structures are formed both from the regression of hydroxyurea-frozen joint DNA molecules and from hydroxyurea-stalled replication forks. These experiments underscore the transient nature of replication fork regression, which becomes detectable due to the hydroxyurea-induced slowing down of replication fork progression.

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Year:  2014        PMID: 24951952     DOI: 10.1007/s00412-014-0471-z

Source DB:  PubMed          Journal:  Chromosoma        ISSN: 0009-5915            Impact factor:   4.316


  32 in total

1.  The importance of repairing stalled replication forks.

Authors:  M M Cox; M F Goodman; K N Kreuzer; D J Sherratt; S J Sandler; K J Marians
Journal:  Nature       Date:  2000-03-02       Impact factor: 49.962

2.  DNA replication-dependent formation of joint DNA molecules in Physarum polycephalum.

Authors:  M Bénard; C Maric; G Pierron
Journal:  Mol Cell       Date:  2001-05       Impact factor: 17.970

3.  Dna2 offers support for stalled forks.

Authors:  Mong Sing Lai; Marco Foiani
Journal:  Cell       Date:  2012-06-08       Impact factor: 41.582

4.  The intra-S phase checkpoint targets Dna2 to prevent stalled replication forks from reversing.

Authors:  Jiazhi Hu; Lei Sun; Fenfen Shen; Yufei Chen; Yu Hua; Yang Liu; Mian Zhang; Yiren Hu; Qingsong Wang; Wei Xu; Fei Sun; Jianguo Ji; Johanne M Murray; Antony M Carr; Daochun Kong
Journal:  Cell       Date:  2012-06-08       Impact factor: 41.582

5.  RNase-dependent discontinuities associated with the crossovers of spontaneously formed joint DNA molecules in Physarum polycephalum.

Authors:  Chrystelle Maric; Marianne Bénard; Gérard Pierron
Journal:  Chromosoma       Date:  2010-07-07       Impact factor: 4.316

Review 6.  Replication origin plasticity, Taylor-made: inhibition vs recruitment of origins under conditions of replication stress.

Authors:  David M Gilbert
Journal:  Chromosoma       Date:  2007-04-03       Impact factor: 4.316

7.  An N-terminal acidic region of Sgs1 interacts with Rpa70 and recruits Rad53 kinase to stalled forks.

Authors:  Anna Maria Hegnauer; Nicole Hustedt; Kenji Shimada; Brietta L Pike; Markus Vogel; Philipp Amsler; Seth M Rubin; Fred van Leeuwen; Aude Guénolé; Haico van Attikum; Nicolas H Thomä; Susan M Gasser
Journal:  EMBO J       Date:  2012-07-20       Impact factor: 11.598

8.  Replication termination at eukaryotic chromosomes is mediated by Top2 and occurs at genomic loci containing pausing elements.

Authors:  Daniele Fachinetti; Rodrigo Bermejo; Andrea Cocito; Simone Minardi; Yuki Katou; Yutaka Kanoh; Katsuhiko Shirahige; Anna Azvolinsky; Virginia A Zakian; Marco Foiani
Journal:  Mol Cell       Date:  2010-08-27       Impact factor: 17.970

9.  Friedreich's ataxia-associated GAA repeats induce replication-fork reversal and unusual molecular junctions.

Authors:  Cindy Follonier; Judith Oehler; Raquel Herrador; Massimo Lopes
Journal:  Nat Struct Mol Biol       Date:  2013-03-03       Impact factor: 15.369

10.  Fork reversal and ssDNA accumulation at stalled replication forks owing to checkpoint defects.

Authors:  José M Sogo; Massimo Lopes; Marco Foiani
Journal:  Science       Date:  2002-07-26       Impact factor: 47.728

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  2 in total

1.  RNase H1 promotes replication fork progression through oppositely transcribed regions of Drosophila mitochondrial DNA.

Authors:  Jose M González de Cózar; Mike Gerards; Eveliina Teeri; Jack George; Eric Dufour; Howard T Jacobs; Priit Jõers
Journal:  J Biol Chem       Date:  2019-01-11       Impact factor: 5.157

Review 2.  Preserving replication fork integrity and competence via the homologous recombination pathway.

Authors:  Anissia Ait Saada; Sarah A E Lambert; Antony M Carr
Journal:  DNA Repair (Amst)       Date:  2018-08-25
  2 in total

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