[HTML][HTML] Compartmentalization of the DNA damage response: Mechanisms and functions
Cells have evolved an arsenal of molecular mechanisms to respond to continuous
alterations in the primary structure of DNA. At the cellular level, DNA damage response …
alterations in the primary structure of DNA. At the cellular level, DNA damage response …
Induction of homologous recombination by site-specific replication stress
MK Triplett, MJ Johnson, LS Symington - DNA repair, 2024 - Elsevier
ABSTRACT DNA replication stress is one of the primary causes of genome instability. In
response to replication stress, cells can employ replication restart mechanisms that rely on …
response to replication stress, cells can employ replication restart mechanisms that rely on …
Control of DNA replication in vitro using a reversible replication barrier
EJ Vontalge, T Kavlashvili, SN Dahmen, MT Cranford… - Nature …, 2024 - nature.com
A major obstacle to studying DNA replication is that it involves asynchronous and highly
delocalized events. A reversible replication barrier overcomes this limitation and allows …
delocalized events. A reversible replication barrier overcomes this limitation and allows …
Comprehensive interactome map** of the DNA repair scaffold SLX4 using proximity labeling and affinity purification
CM Aprosoff, BJA Dyakov, VHW Cheung… - Journal of Proteome …, 2023 - ACS Publications
The DNA repair scaffold SLX4 has pivotal roles in cellular processes that maintain genome
stability, most notably homologous recombination. Germline mutations in SLX4 are …
stability, most notably homologous recombination. Germline mutations in SLX4 are …
Inactivating TDP2 missense mutation in siblings with congenital abnormalities reminiscent of fanconi anemia
G Zagnoli-Vieira, J Brazina, K Van Den Bogaert… - Human Genetics, 2023 - Springer
Mutations in TDP2, encoding tyrosyl-DNA phosphodiesterase 2, have been associated with
a syndromal form of autosomal recessive spinocerebellar ataxia, type 23 (SCAR23). This is …
a syndromal form of autosomal recessive spinocerebellar ataxia, type 23 (SCAR23). This is …
PARP Inhibitors and Proteins Interacting with SLX4
LP Jordheim - Cancers, 2023 - mdpi.com
Simple Summary The aim of this review is to highlight recent work performed on the activity
of a class of cancer drugs (PARP inhibitor) in various cell lines, either expressing or not …
of a class of cancer drugs (PARP inhibitor) in various cell lines, either expressing or not …
[HTML][HTML] Replication fork barriers to study site-specific DNA replication perturbation
J D'Souza, ID Hickson - DNA repair, 2024 - Elsevier
DNA replication ensures the complete and accurate duplication of the genome. The
traditional approach to analysing perturbation of DNA replication is to use chemical …
traditional approach to analysing perturbation of DNA replication is to use chemical …
A local ATR-dependent checkpoint pathway is activated by a site-specific replication fork block in human cells
When replication forks encounter DNA lesions that cause polymerase stalling, a checkpoint
pathway is activated. The ATR-dependent intra-S checkpoint pathway mediates detection …
pathway is activated. The ATR-dependent intra-S checkpoint pathway mediates detection …
Compartmentalization of the SUMO/RNF4 pathway by SLX4 drives DNA repair
E Alghoul, M Paloni, A Takedachi, S Urbach… - Molecular Cell, 2023 - cell.com
SLX4, disabled in the Fanconi anemia group P, is a scaffolding protein that coordinates the
action of structure-specific endonucleases and other proteins involved in the replication …
action of structure-specific endonucleases and other proteins involved in the replication …
The Fanconi anemia pathway induces chromothripsis and ecDNA-driven cancer drug resistance
Chromothripsis describes the catastrophic shattering of mis-segregated chromosomes
trapped within micronuclei. Although micronuclei accumulate DNA double-strand breaks …
trapped within micronuclei. Although micronuclei accumulate DNA double-strand breaks …