Replication fork stalling in late S-phase elicits nascent strand degradation by DNA mismatch repair

E Colicino-Murbach, C Hathaway… - Nucleic Acids …, 2024 - academic.oup.com
Eukaryotic chromosomal replication occurs in a segmented, temporal manner wherein open
euchromatin and compact heterochromatin replicate during early and late S-phase …

RADX prevents genome instability by confining replication fork reversal to stalled forks

A Krishnamoorthy, J Jackson, T Mohamed, M Adolph… - Molecular cell, 2021 - cell.com
RAD51 facilitates replication fork reversal and protects reversed forks from nuclease
degradation. Although potentially a useful replication stress response mechanism …

SMC5/6 promotes replication Fork Stability via negative regulation of the COP9 signalosome

MJ Xu, PW Jordan - International journal of molecular sciences, 2024 - mdpi.com
It is widely accepted that DNA replication fork stalling is a common occurrence during cell
proliferation, but there are robust mechanisms to alleviate this and ensure DNA replication is …

Identification of replication fork-associated proteins in Drosophila embryos and cultured cells using iPOND coupled to quantitative mass spectrometry

A Munden, MT Wright, D Han, R Tirgar, L Plate… - Scientific Reports, 2022 - nature.com
Replication of the eukaryotic genome requires the formation of thousands of replication forks
that must work in concert to accurately replicate the genetic and epigenetic information …

DCAF14 regulates CDT2 to promote SET8-dependent replication fork protection

N Tirado-Class, C Hathaway, A Nelligan… - Life Science …, 2024 - life-science-alliance.org
DDB1-and CUL4-associated factors (DCAFs) CDT2 and DCAF14 are substrate receptors for
Cullin4–RING E3 ubiquitin ligase (CRL4) complexes. CDT2 is responsible for PCNA …

RepID represses megakaryocytic differentiation by recruiting CRL4A-JARID1A at DAB2 promoter

JH Jo, JU Park, YM Kim, SM Ok, DK Kim… - Cell Communication and …, 2023 - Springer
Abstract Background Megakaryocytes (MKs) are platelet precursors, which arise from
hematopoietic stem cells (HSCs). While MK lineage commitment and differentiation are …

A trivalent nucleosome interaction by PHIP/BRWD2 is disrupted in neurodevelopmental disorders and cancer

MAJ Morgan, IK Popova, A Vaidya… - Genes & …, 2021 - genesdev.cshlp.org
Mutations in the PHIP/BRWD2 chromatin regulator cause the human neurodevelopmental
disorder Chung-Jansen syndrome, while alterations in PHIP expression are linked to …

PHIP variants associated with Chung–Jansen syndrome disrupt replication fork stability and genome integrity

N Tirado-Class, C Hathaway… - Molecular …, 2022 - molecularcasestudies.cshlp.org
Chung–Jansen syndrome (CJS) is a rare, autosomal dominant disorder characterized by
developmental delay, intellectual disability/cognitive impairment, behavioral challenges …

The detection of a strong episignature for Chung–Jansen syndrome, partially overlapping with Börjeson–Forssman–Lehmann and White–Kernohan syndromes

N Vos, S Haghshenas, L van der Laan, PKM Russel… - Human Genetics, 2024 - Springer
Chung-Jansen syndrome is a neurodevelopmental disorder characterized by intellectual
disability, behavioral problems, obesity and dysmorphic features. It is caused by pathogenic …

[HTML][HTML] Pathogenic PHIP variants are variably associated with CAKUT

J de Fallois, T Sieckmann, R Schönauer… - Kidney International …, 2024 - Elsevier
Introduction Congenital anomalies of the kidney and urinary tract (CAKUT) represent the
most common cause of chronic kidney disease in children. While only 20% of cases can be …