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Replication Stress, Genomic Instability, and Replication Timing: A Complex Relationship.

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TLDR
In this article, a review of the complex relationship between replication timing, replication stress, and genomic instability is presented, and the results of these studies will potentially facilitate the discovery of new therapeutic pathways, particularly for personalized medicine or new biomarkers.
Abstract
The replication-timing program constitutes a key element of the organization and coordination of numerous nuclear processes in eukaryotes. This program is established at a crucial moment in the cell cycle and occurs simultaneously with the organization of the genome, thus indicating the vital significance of this process. With recent technological achievements of high-throughput approaches, a very strong link has been confirmed between replication timing, transcriptional activity, the epigenetic and mutational landscape, and the 3D organization of the genome. There is also a clear relationship between replication stress, replication timing, and genomic instability, but the extent to which they are mutually linked to each other is unclear. Recent evidence has shown that replication timing is affected in cancer cells, although the cause and consequence of this effect remain unknown. However, in-depth studies remain to be performed to characterize the molecular mechanisms of replication-timing regulation and clearly identify different cis- and trans-acting factors. The results of these studies will potentially facilitate the discovery of new therapeutic pathways, particularly for personalized medicine, or new biomarkers. This review focuses on the complex relationship between replication timing, replication stress, and genomic instability.

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Journal ArticleDOI

RETSAT associates with DDX39B to promote fork restarting and resistance to gemcitabine based chemotherapy in pancreatic ductal adenocarcinoma

TL;DR: In this article , the role of RETSAT in replication stress resistance and hypoxia adaptation in pancreatic ductal adenocarcinoma (PDAC) cells, and decipher the underlying mechanism.
Journal ArticleDOI

Mapping Replication Timing in Single Mammalian Cells

TL;DR: An improved single‐cell Repli‐seq protocol that uses degenerate oligonucleotide–primed PCR (DOP‐PCR) for uniform whole‐genome amplification and uniquely barcoded primers that permit early pooling of single‐ cell samples into a single library preparation is described.
Journal ArticleDOI

Both phosphorylation and phosphatase activity of PTEN are required to prevent replication fork progression during stress by inducing heterochromatin.

TL;DR: In this paper , the association between the catalytic function of PTEN regulated by posttranslational modulation and cellular response to replication stress has been studied explicitly, and it was shown that PTEN-null cells display unrestrained replication fork progression with accumulation of damaged DNA after treatment with aphidicolin which can be rescued by ectopic expression of full-length PTEN.
Journal ArticleDOI

RIF1 Links Replication Timing with Fork Reactivation and DNA Double-Strand Break Repair

TL;DR: The role of RIF1 is associated with binding G4-quadruplexes and changes in 3D chromatin that may suppress origin activation over a long distance as discussed by the authors.
References
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Journal ArticleDOI

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Michael S. Lawrence, +96 more
- 11 Jul 2013 - 
TL;DR: A fundamental problem with cancer genome studies is described: as the sample size increases, the list of putatively significant genes produced by current analytical methods burgeons into the hundreds and the list includes many implausible genes, suggesting extensive false-positive findings that overshadow true driver events.
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Journal ArticleDOI

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Journal ArticleDOI

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TL;DR: In this paper, the kinase ATR (ATM- and Rad3-related) stabilizes and helps to restart stalled replication forks, avoiding the generation of DNA damage and genome instability.
Journal ArticleDOI

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TL;DR: Finite cycles of TCR at naturally occurring non-canonical DNA structures might contribute to genomic instability and genetic disease.
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