Search Results - "Jeggo, Penelope A"
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The Repair and Signaling Responses to DNA Double-Strand Breaks
Published in Advances in Genetics (2013)“…A DNA double-strand break (DSB) has long been recognized as a severe cellular lesion, potentially representing an initiating event for carcinogenesis or cell…”
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53BP1-dependent robust localized KAP-1 phosphorylation is essential for heterochromatic DNA double-strand break repair
Published in Nature cell biology (01-02-2010)“…DNA double-strand breaks (DSBs) trigger ATM (ataxia telangiectasia mutated) signalling and elicit genomic rearrangements and chromosomal fragmentation if…”
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ATM Localization and Heterochromatin Repair Depend on Direct Interaction of the 53BP1-BRCT2 Domain with γH2AX
Published in Cell reports (Cambridge) (15-12-2015)“…53BP1 plays multiple roles in mammalian DNA damage repair, mediating pathway choice and facilitating DNA double-strand break repair in heterochromatin…”
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4
The complexity of DNA double strand breaks is a critical factor enhancing end-resection
Published in DNA repair (01-11-2013)“…•Heavy ion beam-induced complex DSBs efficiently activate DNA end resection.•Up to 85% of complex DSBs undergo resection in G2 cells.•Around 20–40% of human G1…”
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Cilia defects upon loss of WDR4 are linked to proteasomal hyperactivity and ubiquitin shortage
Published in Cell death & disease (09-09-2024)“…The WD repeat-containing protein 4 (WDR4) has repeatedly been associated with primary microcephaly, a condition of impaired brain and skull growth. Often,…”
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Diminished origin-licensing capacity specifically sensitizes tumor cells to replication stress
Published in Molecular cancer research (01-04-2013)“…Previous studies have shown that dormant licensed replication origins can be exploited to enhance recovery from replication stress. Since tumor cells express…”
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Journal Article -
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KAP-1 phosphorylation regulates CHD3 nucleosome remodeling during the DNA double-strand break response
Published in Nature structural & molecular biology (01-07-2011)“…Heterochromatin factor KAP-1 is phosphorylated by ATM during the DNA damage response. Now the functional consequences of this modification are explored,…”
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Impaired lymphocyte development and antibody class switching and increased malignancy in a murine model of DNA ligase IV syndrome
Published in The Journal of clinical investigation (01-06-2009)“…Hypomorphic mutations in DNA ligase IV (LIG4) cause a human syndrome of immunodeficiency, radiosensitivity, and growth retardation due to defective DNA repair…”
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Distinct response of adult neural stem cells to low versus high dose ionising radiation
Published in DNA repair (01-04-2019)“…•Apoptosis arises linearly with the radiation dose in adult neural progenitor cells.•Proliferation arrest and differentiation are inefficiently activated at…”
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DNA repair is limiting for haematopoietic stem cells during ageing
Published in Nature (07-06-2007)“…Accumulation of DNA damage leading to adult stem cell exhaustion has been proposed to be a principal mechanism of ageing. Here we address this question by…”
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Establishing mechanisms affecting the individual response to ionizing radiation
Published in International journal of radiation biology (03-03-2020)“…Purpose: Humans are increasingly exposed to ionizing radiation (IR). Both low (<100 mGy) and high doses can cause stochastic effects, including cancer; whereas…”
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Phosphoproteomic analysis reveals that PP4 dephosphorylates KAP-1 impacting the DNA damage response
Published in The EMBO journal (16-05-2012)“…Protein phosphatase PP4C has been implicated in the DNA damage response (DDR), but its substrates in DDR remain largely unknown. We devised a novel proteomic…”
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Resting cells rely on the DNA helicase component MCM2 to build cilia
Published in Nucleic acids research (10-01-2019)“…Abstract Minichromosome maintenance (MCM) proteins facilitate replication by licensing origins and unwinding the DNA double strand. Interestingly, the number…”
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Analysis of cilia dysfunction phenotypes in zebrafish embryos depleted of Origin recognition complex factors
Published in European journal of human genetics : EJHG (01-05-2019)“…Meier-Gorlin syndrome (MGS) is a rare, congenital primordial microcephalic dwarfism disorder. MGS is caused by genetic variants of components of the origin…”
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The life and death of DNA-PK
Published in Oncogene (03-02-2005)“…Double-strand breaks (DSBs) arise endogenously during normal cellular processes and exogenously by genotoxic agents such as ionizing radiation (IR). DSBs are…”
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Normal cellular radiosensitivity in an adult Fanconi anaemia patient with marked clinical radiosensitivity
Published in Radiotherapy and oncology (01-07-2001)“…Background: Fanconi anaemia is a rare disease associated with cellular sensitivity to chemicals (e.g. mitomycin C and diepoxybutane); variable but mild…”
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Reduced joining of DNA ends correlates with chromosomal instability in three melanoma cell lines
Published in Tumor biology (01-03-2003)“…Chromosomal instability plays a pivotal role in multistep carcinogenesis by facilitating the acquisition of the multiple genetic alterations necessary for…”
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Chapter One - The Repair and Signaling Responses to DNA Double-Strand Breaks
Published in Advances in genetics (01-01-2013)“…A DNA double-strand break (DSB) has long been recognized as a severe cellular lesion, potentially representing an initiating event for carcinogenesis or cell…”
Get full text
Journal Article -
19
ATM Localization and Heterochromatin Repair Depend on Direct Interaction of the 53BP1-BRCT 2 Domain with γH2AX
Published in Cell reports (Cambridge) (01-12-2015)Get full text
Journal Article -
20
Phosphoproteomic analysis reveals that PP4 dephosphorylates KAP-1 impacting the DNA damage response: PP4 regulates KAP-1 function in DDR
Published in The EMBO journal (16-05-2012)Get full text
Journal Article