53BP1, BRCA1, and the choice between recombination and end joining at DNA double-strand breaks
JM Daley, P Sung - Molecular and cellular biology, 2014 - Taylor & Francis
When DNA double-strand breaks occur, the cell cycle stage has a major influence on the
choice of the repair pathway employed. Specifically, nonhomologous end joining is the …
choice of the repair pathway employed. Specifically, nonhomologous end joining is the …
The Ku heterodimer: function in DNA repair and beyond
VL Fell, C Schild-Poulter - Mutation Research/Reviews in Mutation …, 2015 - Elsevier
Ku is an abundant, highly conserved DNA binding protein found in both prokaryotes and
eukaryotes that plays essential roles in the maintenance of genome integrity. In eukaryotes …
eukaryotes that plays essential roles in the maintenance of genome integrity. In eukaryotes …
GUARDIN is a p53-responsive long non-coding RNA that is essential for genomic stability
The list of long non-coding RNAs (lncRNAs) involved in the p53 pathway of the DNA
damage response is rapidly expanding, but whether lncRNAs have a role in maintaining the …
damage response is rapidly expanding, but whether lncRNAs have a role in maintaining the …
DNA repair factor BRCA1 depletion occurs in Alzheimer brains and impairs cognitive function in mice
E Suberbielle, B Djukic, M Evans, DH Kim… - Nature …, 2015 - nature.com
Maintaining DNA integrity is vital for all cells and organisms. Defective DNA repair may
contribute to neurological disorders, including Alzheimer's disease (AD). We found reduced …
contribute to neurological disorders, including Alzheimer's disease (AD). We found reduced …
[HTML][HTML] Alternative end-joining pathway (s): bricolage at DNA breaks
P Frit, N Barboule, Y Yuan, D Gomez, P Calsou - DNA repair, 2014 - Elsevier
To cope with DNA double strand break (DSB) genotoxicity, cells have evolved two main
repair pathways: homologous recombination which uses homologous DNA sequences as …
repair pathways: homologous recombination which uses homologous DNA sequences as …
A role for human homologous recombination factors in suppressing microhomology-mediated end joining
S Ahrabi, S Sarkar, SX Pfister, G Pirovano… - Nucleic acids …, 2016 - academic.oup.com
DNA double-strand breaks (DSBs) are toxic lesions, which if improperly repaired can result
in cell death or genomic instability. DSB repair is usually facilitated by the classical non …
in cell death or genomic instability. DSB repair is usually facilitated by the classical non …
PARP3 affects the relative contribution of homologous recombination and nonhomologous end-joining pathways
C Beck, C Boehler, J Guirouilh Barbat… - Nucleic acids …, 2014 - academic.oup.com
The repair of toxic double-strand breaks (DSB) is critical for the maintenance of genome
integrity. The major mechanisms that cope with DSB are: homologous recombination (HR) …
integrity. The major mechanisms that cope with DSB are: homologous recombination (HR) …
Reactivation of HIV latency by a newly modified Ingenol derivative via protein kinase Cδ–NF-κB signaling
Objective: Although HAART effectively suppresses viral replication, it fails to eradicate latent
viral reservoirs. The 'shock and kill'strategy involves the activation of HIV from latent …
viral reservoirs. The 'shock and kill'strategy involves the activation of HIV from latent …
DNA replication initiation shapes the mutational landscape and expression of the human genome
P Murat, C Perez, A Crisp, P van Eijk, SH Reed… - Science …, 2022 - science.org
The interplay between active biological processes and DNA repair is central to mutagenesis.
Here, we show that the ubiquitous process of replication initiation is mutagenic, leaving a …
Here, we show that the ubiquitous process of replication initiation is mutagenic, leaving a …
Genomic rearrangements induced by unscheduled DNA double strand breaks in somatic mammalian cells
A So, T Le Guen, BS Lopez… - The FEBS …, 2017 - Wiley Online Library
DNA double‐strand breaks (DSB s) are highly toxic lesions that can lead to profound
genome rearrangements and/or cell death. They routinely occur in genomes due to …
genome rearrangements and/or cell death. They routinely occur in genomes due to …