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Journal ArticleDOI

Interplay of replication checkpoints and repair proteins at stalled replication forks.

Dana Branzei, +1 more
- 01 Jul 2007 - 
- Vol. 6, Iss: 7, pp 994-1003
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TLDR
This review focuses mainly on the results obtained in budding yeast on the multiple roles of checkpoints in maintaining fork integrity and on the enzymatic activities that cooperate with the checkpoint pathway to promote fork resumption and repair of DNA lesions thereby contributing to genome integrity.
About
This article is published in DNA Repair.The article was published on 2007-07-01. It has received 144 citations till now. The article focuses on the topics: Control of chromosome duplication & DNA re-replication.

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Citations
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Formation of Dicentric and Acentric Chromosomes, by a Template Switch Mechanism, in Budding Yeast

TL;DR: This chapter discusses the many forms of genome rearrangements, general mechanisms underlying genome rearranging, and the five degrees of freedom in replication fork recovery.

Checkpoint Regulation of Replication Forks in Response to DNA Damage: A Dissertation

TL;DR: This thesis work found a wide variety of mutants which either completely or partially failed to slow replication in response to DNA damage, and observed that the RecQ helicase Rqh1, implicated in negatively regulating recombination, was required for slowing.
Dissertation

Analysis of chromosomal rearrangements after replication restart

Saed Mohebi
TL;DR: The work in this thesis analyses the timing of replication restart and appearance of chromosomal rearrangements in a single cell cycle after induction of fork stalling and identifies the recombination-dependent intermediates corresponding to the two pathways of rearrangement.
Dissertation

Investigating fork rotation and DNA pre-catenation in Saccharomyces cerevisiae

TL;DR: It is shown that Tof1/Timeless and Csm3/Tipin proteins regulate DNA replication and prevent chronic genome instability by minimizing pre-catenation during DNA replication.
References
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Journal ArticleDOI

RAD6 -dependent DNA repair is linked to modification of PCNA by ubiquitin and SUMO

TL;DR: It is shown that UBC9, a small ubiquitin-related modifier (SUMO)-conjugating enzyme, is also affiliated with this pathway and that proliferating cell nuclear antigen (PCNA) is a substrate, and that damage-induced PCNA ubiquitination is elementary for DNA repair and occurs at the same conserved residue in yeast and humans.
Journal ArticleDOI

Multiple Pathways of Recombination Induced by Double-Strand Breaks in Saccharomyces cerevisiae

TL;DR: This review encompasses different aspects of DSB-induced recombination in Saccharomyces and attempts to relate genetic, molecular biological, and biochemical studies of the processes of DNA repair and recombination.
Journal ArticleDOI

The Bloom's syndrome helicase suppresses crossing over during homologous recombination

TL;DR: It is shown that mutations in BLM and hTOPO IIIα together effect the resolution of a recombination intermediate containing a double Holliday junction and prevents exchange of flanking sequences, which has wider implications for the understanding of the process of homologous recombination and the mechanisms that exist to prevent tumorigenesis.
Journal ArticleDOI

Choreography of the DNA damage response: Spatiotemporal relationships among checkpoint and repair proteins

TL;DR: The cellular response to DSBs and DNA replication stress is likely directed by the Mre11 complex detecting and processing DNA ends in conjunction with Sae2 and by RP-A recognizing single-stranded DNA and recruiting additional checkpoint and repair proteins.
Journal ArticleDOI

Replication Dynamics of the Yeast Genome

TL;DR: Oligonucleotide microarrays were used to map the detailed topography of chromosome replication in the budding yeast Saccharomyces cerevisiae, finding the two ends of each of the 16 chromosomes are highly correlated in their times of replication.
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