Maintaining genome integrity: Protein kinases and phosphatases orchestrate the balancing act of DNA double-strand breaks repair in cancer

S Qin, I Kitty, Y Hao, F Zhao, W Kim - International Journal of Molecular …, 2023 - mdpi.com
DNA double-strand breaks (DSBs) are the most lethal DNA damages which lead to severe
genome instability. Phosphorylation is one of the most important protein post-translation …

MCPH1: a window into brain development and evolution

JN Pulvers, N Journiac, Y Arai… - Frontiers in cellular …, 2015 - frontiersin.org
The development of the mammalian cerebral cortex involves a series of mechanisms: from
patterning, progenitor cell proliferation and differentiation, to neuronal migration. Many …

RB localizes to DNA double-strand breaks and promotes DNA end resection and homologous recombination through the recruitment of BRG1

R Vélez-Cruz, S Manickavinayaham… - Genes & …, 2016 - genesdev.cshlp.org
The retinoblastoma (RB) tumor suppressor is recognized as a master regulator that controls
entry into the S phase of the cell cycle. Its loss leads to uncontrolled cell proliferation and is a …

Microcephalin 1/BRIT1-TRF2 interaction promotes telomere replication and repair, linking telomere dysfunction to primary microcephaly

A Cicconi, R Rai, X Xiong, C Broton… - Nature …, 2020 - nature.com
Telomeres protect chromosome ends from inappropriately activating the DNA damage and
repair responses. Primary microcephaly is a key clinical feature of several human telomere …

RNAi-Based Suppressor Screens Reveal Genetic Interactions Between the CRL2LRR-1 E3-Ligase and the DNA Replication Machinery in Caenorhabditis elegans

B Ossareh-Nazari, A Katsiarimpa… - G3: Genes, Genomes …, 2016 - academic.oup.com
Abstract Cullin-RING E3-Ligases (CRLs), the largest family of E3 ubiquitin-Ligases, regulate
diverse cellular processes by promoting ubiquitination of target proteins. The evolutionarily …

Microcephaly family protein MCPH1 stabilizes RAD51 filaments

HY Chang, CY Lee, CH Lu, W Lee… - Nucleic Acids …, 2020 - academic.oup.com
Abstract Microcephalin 1 (MCPH1) was identified from genetic mutations in patients with
primary autosomal recessive microcephaly. In response to DNA double-strand breaks …

Ataxia-telangiectasia and Nijmegen breakage syndrome

J Kobayashi - DNA Repair Disorders, 2019 - Springer
Ataxia-telangiectasia (AT) and Nijmegen breakage syndrome (NBS) are well-known single-
gene disorders, which have similar cellular phenotypes, including chromosome instability …

[PDF][PDF] BRCA1 和TopBP1 表达与非小细胞肺癌含铂方案疗效的相关性研究

汪洋, 王临润, 陈建, 李银燕, 孙浩珍… - 中国药学 …, 2015 - journal11.magtechjournal.com
目的探讨DNA 损伤修复蛋白乳腺癌易感基因-1 (BRCA1) 和拓扑异构酶Ⅱβ 结合蛋白1
(TopBP1) 表达与非小细胞肺癌(non-small cell lung cancer, NSCLC) 含铂方案疗效的相关性 …

Utilization of High Throughput Screening to Identify Therapeutic Targets for Defective MCPH1/BRIT1 Function-Induced Premature Chromosome Condensation in …

AA Awaji - 2016 - etheses.whiterose.ac.uk
Mutations in the N-terminal region of MCPH1/BRIT1 cause premature chromosome
condensation (PCC), whereby cells enter mitosis before completing DNA replication. 792 …

[图书][B] Regulation of the ATR Pathway in the Replication Stress Response

JW Luzwick - 2016 - search.proquest.com
Results.......................................................................................................................... 60 Mutation of
Serine 1333 alters ATR kinase activity............................................. 60 S1333 is unlikely to be …