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Open AccessJournal ArticleDOI

Regulation of homologous recombination in eukaryotes

TLDR
The factors and mechanistic stages of recombination that are subject to regulation are reviewed and it is suggested that recombination achieves flexibility and robustness by proceeding through metastable, reversible intermediates.
Abstract
Homologous recombination (HR) is required for accurate chromosome segregation during the first meiotic division and constitutes a key repair and tolerance pathway for complex DNA damage, including DNA double-strand breaks, interstrand crosslinks, and DNA gaps. In addition, recombination and replication are inextricably linked, as recombination recovers stalled and broken replication forks, enabling the evolution of larger genomes/replicons. Defects in recombination lead to genomic instability and elevated cancer predisposition, demonstrating a clear cellular need for recombination. However, recombination can also lead to genome rearrangements. Unrestrained recombination causes undesired endpoints (translocation, deletion, inversion) and the accumulation of toxic recombination intermediates. Evidently, HR must be carefully regulated to match specific cellular needs. Here, we review the factors and mechanistic stages of recombination that are subject to regulation and suggest that recombination achieves fle...

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Journal ArticleDOI

Repair Pathway Choices and Consequences at the Double-Strand Break

TL;DR: Alternative error-prone DSB repair pathways, namely alternative end joining (alt-EJ) and single-strand annealing (SSA) have been recently shown to operate in many different conditions and to contribute to genome rearrangements and oncogenic transformation.
Journal ArticleDOI

Genome editing with CRISPR–Cas nucleases, base editors, transposases and prime editors

TL;DR: This work analyzes key considerations when choosing genome editing agents and identifies opportunities for future improvements and applications in basic research and therapeutics.
Journal ArticleDOI

Enhanced homology-directed human genome engineering by controlled timing of CRISPR/Cas9 delivery.

TL;DR: It is shown here that new genetic information can be introduced site-specifically and with high efficiency by homology-directed repair (HDR) of Cas9-induced site- specific double-strand DNA breaks using timed delivery ofCas9-guide RNA ribonucleoprotein (RNP) complexes.
Journal ArticleDOI

Double-strand break repair: 53BP1 comes into focus

TL;DR: A model is emerging in which 53BP1 recruitment requires the direct recognition of a DSB-specific histone code and its influence on pathway choice is mediated by mutual antagonism with breast cancer 1 (BRCA1).
Journal ArticleDOI

CRISPR-Based Technologies for the Manipulation of Eukaryotic Genomes.

TL;DR: Recent developments that extend the generality, DNA specificity, product selectivity, and fundamental capabilities of natural CRISPR systems are described.
References
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Journal ArticleDOI

Genome maintenance mechanisms for preventing cancer

TL;DR: This review summarizes the main DNA caretaking systems and their impact on genome stability and carcinogenesis.
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

Rates of Spontaneous Mutation

TL;DR: It is now possible to specify some of the evolutionary forces that shape these diverse mutation rates in broad groups of organisms.
Journal ArticleDOI

Mechanism of eukaryotic homologous recombination.

TL;DR: HR accessory factors that facilitate other stages of the Rad51- and Dmc1-catalyzed homologous DNA pairing and strand exchange reaction have also been identified.
Journal ArticleDOI

Human CtIP promotes DNA end resection

TL;DR: These findings establish evolutionarily conserved roles for CtIP-like proteins in controlling DSB resection, checkpoint signalling and homologous recombination.
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