Literature DB >> 16793417

Methods to study replication fork collapse in budding yeast.

Giordano Liberi1, Cecilia Cotta-Ramusino, Massimo Lopes, Jose' Sogo, Chiara Conti, Aaron Bensimon, Marco Foiani.   

Abstract

Replication of the eukaryotic genome is a difficult task, as cells must coordinate chromosome replication with chromatin remodeling, DNA recombination, DNA repair, transcription, cell cycle progression, and sister chromatid cohesion. Yet, DNA replication is a potentially genotoxic process, particularly when replication forks encounter a bulge in the template: forks under these conditions may stall and restart or even break down leading to fork collapse. It is now clear that fork collapse stimulates chromosomal rearrangements and therefore represents a potential source of DNA damage. Hence, the comprehension of the mechanisms that preserve replication fork integrity or that promote fork collapse are extremely relevant for the understanding of the cellular processes controlling genome stability. Here we describe some experimental approaches that can be used to physically visualize the quality of replication forks in the yeast S. cerevisiae and to distinguish between stalled and collapsed forks.

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Year:  2006        PMID: 16793417     DOI: 10.1016/S0076-6879(05)09026-9

Source DB:  PubMed          Journal:  Methods Enzymol        ISSN: 0076-6879            Impact factor:   1.600


  26 in total

1.  Shu proteins promote the formation of homologous recombination intermediates that are processed by Sgs1-Rmi1-Top3.

Authors:  Hocine W Mankouri; Hien-Ping Ngo; Ian D Hickson
Journal:  Mol Biol Cell       Date:  2007-08-01       Impact factor: 4.138

Review 2.  Quality control of DNA break metabolism: in the 'end', it's a good thing.

Authors:  Roland Kanaar; Claire Wyman; Rodney Rothstein
Journal:  EMBO J       Date:  2008-02-20       Impact factor: 11.598

3.  Resolution by unassisted Top3 points to template switch recombination intermediates during DNA replication.

Authors:  M Rebecca Glineburg; Alejandro Chavez; Vishesh Agrawal; Steven J Brill; F Brad Johnson
Journal:  J Biol Chem       Date:  2013-10-07       Impact factor: 5.157

4.  The S-phase checkpoint is required to respond to R-loops accumulated in THO mutants.

Authors:  Belén Gómez-González; Irene Felipe-Abrio; Andrés Aguilera
Journal:  Mol Cell Biol       Date:  2009-08-03       Impact factor: 4.272

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

Authors:  Chrystelle Maric; Marianne Bénard
Journal:  Chromosoma       Date:  2014-06-21       Impact factor: 4.316

6.  Homologous recombination-dependent rescue of deficiency in the structural maintenance of chromosomes (Smc) 5/6 complex.

Authors:  Alejandro Chavez; Vishesh Agrawal; F Brad Johnson
Journal:  J Biol Chem       Date:  2010-12-07       Impact factor: 5.157

7.  Timeless-dependent DNA replication-coupled recombination promotes Kaposi's Sarcoma-associated herpesvirus episome maintenance and terminal repeat stability.

Authors:  Jayaraju Dheekollu; Horng-Shen Chen; Kenneth M Kaye; Paul M Lieberman
Journal:  J Virol       Date:  2013-01-16       Impact factor: 5.103

Review 8.  Tus-Ter as a tool to study site-specific DNA replication perturbation in eukaryotes.

Authors:  Nicolai B Larsen; Ian D Hickson; Hocine W Mankouri
Journal:  Cell Cycle       Date:  2014       Impact factor: 4.534

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.  SRS2 and SGS1 prevent chromosomal breaks and stabilize triplet repeats by restraining recombination.

Authors:  Alix Kerrest; Ranjith P Anand; Rangapriya Sundararajan; Rodrigo Bermejo; Giordano Liberi; Bernard Dujon; Catherine H Freudenreich; Guy-Franck Richard
Journal:  Nat Struct Mol Biol       Date:  2009-01-11       Impact factor: 15.369

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