The Werner syndrome protein is required for recruitment of chromatin assembly factor 1 following DNA damage (Q48336289)

10 February 2018

title

The Werner syndrome protein is required for recruitment of chromatin assembly factor 1 following DNA damage (English)

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10 February 2018

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R Jiao

1

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10 February 2018

J A Harrigan

2

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10 February 2018

I Shevelev

3

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10 February 2018

T Dietschy

4

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10 February 2018

N Selak

5

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10 February 2018

F E Indig

6

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10 February 2018

J Piotrowski

7

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10 February 2018

P Janscak

8

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10 February 2018

V A Bohr

9

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10 February 2018

I Stagljar

10

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10 February 2018

language of work or name

English

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publication date

18 December 2006

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10 February 2018

published in

Oncogene

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10 February 2018

volume

26

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10 February 2018

issue

26

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10 February 2018

page(s)

3811-3822

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10 February 2018

Chromatin disassembly mediated by the histone chaperone Asf1 is essential for transcriptional activation of the yeast PHO5 and PHO8 genes

cites work

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https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Deficient DNA repair in the human progeroid disorder, Werner syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Human telomeric protein TRF2 associates with genomic double-strand breaks as an early response to DNA damage.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Linkage between Werner syndrome protein and the Mre11 complex via Nbs1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Physical and functional mapping of the replication protein a interaction domain of the werner and bloom syndrome helicases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Werner syndrome protein and the MRE11 complex are involved in a common pathway of replication fork recovery

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Chromatin assembly coupled to DNA repair: a new role for chromatin assembly factor I.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

RPA alleviates the inhibitory effect of vinylphosphonate internucleotide linkages on DNA unwinding by BLM and WRN helicases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Local action of the chromatin assembly factor CAF-1 at sites of nucleotide excision repair in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Formation of a nuclear complex containing the p53 tumor suppressor, YB-1, and the Werner syndrome gene product in cells treated with UV light

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

The Werner syndrome protein stimulates DNA polymerase beta strand displacement synthesis via its helicase activity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

The Werner syndrome protein operates in base excision repair and cooperates with DNA polymerase beta

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

RecQ helicases: caretakers of the genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Chromatin assembly factor 1 is essential and couples chromatin assembly to DNA replication in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Physical and functional interaction between the Bloom's syndrome gene product and the largest subunit of chromatin assembly factor 1

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Cellular dynamics and modulation of WRN protein is DNA damage specific

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Werner protein is a target of DNA-dependent protein kinase in vivo and in vitro, and its catalytic activities are regulated by phosphorylation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Ku heterodimer binds to both ends of the Werner protein and functional interaction occurs at the Werner N-terminus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Ultraviolet radiation sensitivity and reduction of telomeric silencing in Saccharomyces cerevisiae cells lacking chromatin assembly factor-I.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

The p150 and p60 subunits of chromatin assembly factor I: a molecular link between newly synthesized histones and DNA replication

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Chromatin assembly factor 1 (CAF-1) colocalizes with replication foci in HeLa cell nuclei

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Chromatin assembly during DNA replication in somatic cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Ethidium bromide provides a simple tool for identifying genuine DNA-independent protein associations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Elevated telomere-telomere recombination in WRN-deficient, telomere dysfunctional cells promotes escape from senescence and engagement of the ALT pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Modulation of Werner syndrome protein function by a single mutation in the conserved RecQ domain

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Functional interaction between Ku and the werner syndrome protein in DNA end processing

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Accumulation of Werner protein at DNA double-strand breaks in human cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

The yeast histone chaperone chromatin assembly factor 1 protects against double-strand DNA-damaging agents

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Crystal structure of the nucleosome core particle at 2.8 A resolution

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Nucleolar localization of the Werner syndrome protein in human cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Recruitment of phosphorylated chromatin assembly factor 1 to chromatin after UV irradiation of human cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

A CAF-1-PCNA-mediated chromatin assembly pathway triggered by sensing DNA damage

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Silencing of chromatin assembly factor 1 in human cells leads to cell death and loss of chromatin assembly during DNA synthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Induction of CAF-1 expression in response to DNA strand breaks in quiescent human cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Junction of RecQ helicase biochemistry and human disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Werner syndrome and the function of the Werner protein; what they can teach us about the molecular aging process.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

The Werner syndrome helicase and exonuclease cooperate to resolve telomeric D loops in a manner regulated by TRF1 and TRF2

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Telomere-binding protein TRF2 binds to and stimulates the Werner and Bloom syndrome helicases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

A functional interaction of Ku with Werner exonuclease facilitates digestion of damaged DNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Current advances in unraveling the function of the Werner syndrome protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

The Bloom's syndrome helicase interacts directly with the human DNA mismatch repair protein hMSH6.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Nucleotide excision repair in yeast

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Characterisation of the interaction between WRN, the helicase/exonuclease defective in progeroid Werner's syndrome, and an essential replication factor, PCNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Werner helicase relocates into nuclear foci in response to DNA damaging agents and co-localizes with RPA and Rad51.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

In vivo function of the conserved non-catalytic domain of Werner syndrome helicase in DNA replication

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

The interaction site of Flap Endonuclease-1 with WRN helicase suggests a coordination of WRN and PCNA

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Stimulation of flap endonuclease-1 by the Bloom's syndrome protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Characterization of Werner syndrome protein DNA helicase activity: directionality, substrate dependence and stimulation by replication protein A

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Replication-dependent marking of DNA by PCNA facilitates CAF-1-coupled inheritance of chromatin

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Purification and characterization of CAF-I, a human cell factor required for chromatin assembly during DNA replication in vitro

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

p53-mediated apoptosis is attenuated in Werner syndrome cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Werner protein recruits DNA polymerase delta to the nucleolus

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

The p55 subunit of Drosophila chromatin assembly factor 1 is homologous to a histone deacetylase-associated protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Interaction between the Drosophila CAF-1 and ASF1 chromatin assembly factors

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Nucleosome assembly by a complex of CAF-1 and acetylated histones H3/H4

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Central Role for the Werner Syndrome Protein/Poly(ADP-Ribose) Polymerase 1 Complex in the Poly(ADP-Ribosyl)ation Pathway after DNA Damage

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Poly(ADP-ribose) polymerase 1 regulates both the exonuclease and helicase activities of the Werner syndrome protein

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Colocalization, physical, and functional interaction between Werner and Bloom syndrome proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Functional interaction of p53 and BLM DNA helicase in apoptosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

The Bloom's syndrome gene product interacts with topoisomerase III

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

The processing of Holliday junctions by BLM and WRN helicases is regulated by p53

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

Positional cloning of the Werner's syndrome gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

The human Rothmund-Thomson syndrome gene product, RECQL4, localizes to distinct nuclear foci that coincide with proteins involved in the maintenance of genome stability

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

inferred from DOI database lookup

7 January 2021

based on heuristic

A minimal exonuclease domain of WRN forms a hexamer on DNA and possesses both 3'- 5' exonuclease and 5'-protruding strand endonuclease activities

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

inferred from DOI database lookup

7 January 2021

based on heuristic

Defective S phase chromatin assembly causes DNA damage, activation of the S phase checkpoint, and S phase arrest

1 reference

https://api.crossref.org/works/10.1038%2FSJ.ONC.1210150

inferred from DOI database lookup

7 January 2021

based on heuristic

Identifiers

DOI

10.1038/SJ.ONC.1210150

1 reference

10 February 2018

1 reference

10 February 2018