The processing of Holliday junctions by BLM and WRN helicases is regulated by p53 (Q28206425)

13

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Vilhelm A. Bohr

16

object named as

Vilhelm A Bohr

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author name string

Qin Yang

1

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Ran Zhang

2

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Xin Wei Wang

3

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Elisa A Spillare

4

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Steven P Linke

5

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Deepa Subramanian

6

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Jack D Griffith

7

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Ji Liang Li

8

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Ian D Hickson

9

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Jiang Cheng Shen

10

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Lawrence A Loeb

11

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Sharlyn J Mazur

12

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Robert M Brosh

14

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Parimal Karmakar

15

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Curtis C Harris

Journal of Biological Chemistry

17

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language of work or name

English

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publication date

30 August 2002

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published in

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volume

277

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issue

35

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page(s)

31980-7

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cites work

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The Bloom's syndrome gene product interacts with topoisomerase III

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Functional interaction between the Werner Syndrome protein and DNA polymerase delta

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Werner protein recruits DNA polymerase delta to the nucleolus

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The Bloom's and Werner's syndrome proteins are DNA structure-specific helicases

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Werner's syndrome protein (WRN) migrates Holliday junctions and co-localizes with RPA upon replication arrest

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The Bloom's syndrome gene product promotes branch migration of holliday junctions

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Surfing the p53 network

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Regulation of the p53 tumor suppressor protein

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Increase of spontaneous intrachromosomal homologous recombination in mammalian cells expressing a mutant p53 protein

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Inactivation of p53 results in high rates of homologous recombination

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Interaction of p53 with the human Rad51 protein

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Tumor suppressor protein p53 binds preferentially to supercoiled DNA.

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Physical and functional interaction between p53 and the Werner's syndrome protein

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p53-mediated apoptosis is attenuated in Werner syndrome cells

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Functional interaction of p53 and BLM DNA helicase in apoptosis

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Functional and physical interaction between WRN helicase and human replication protein A

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Oligomeric ring structure of the Bloom's syndrome helicase

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Wild-type but not mutant p53 immunopurified proteins bind to sequences adjacent to the SV40 origin of replication

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RecG helicase activity at three- and four-strand DNA structures.

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p53 Modulates the exonuclease activity of Werner syndrome protein

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Electron microscope visualization of chromatin and other DNA-protein complexes

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Regulation of the sequence-specific DNA binding function of p53 by protein kinase C and protein phosphatases

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Identification of p53 as a sequence-specific DNA-binding protein

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Activation of the cryptic DNA binding function of mutant forms of p53.

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Regulation of the specific DNA binding function of p53

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Relaxing and unwinding on Holliday: DNA helicase-mediated branch migration

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Crystal structure of DNA recombination protein RuvA and a model for its binding to the Holliday junction

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BLM, the Bloom's syndrome protein, varies during the cell cycle in its amount, distribution, and co-localization with other nuclear proteins

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Post-translational modifications and activation of p53 by genotoxic stresses

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Covalent and noncovalent modifiers of the p53 protein

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ATM-dependent activation of p53 involves dephosphorylation and association with 14-3-3 proteins

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Potential role for the BLM helicase in recombinational repair via a conserved interaction with RAD51

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Regulation and localization of the Bloom syndrome protein in response to DNA damage

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Regulation of ubiquitination and degradation of p53 in unstressed cells through C-terminal phosphorylation

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Stabilization and activation of p53 are regulated independently by different phosphorylation events

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Posttranslational modifications of p53 in replicative senescence overlapping but distinct from those induced by DNA damage

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The Werner syndrome gene product co-purifies with the DNA replication complex and interacts with PCNA and topoisomerase I.

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Bloom's syndrome. XIX. Cytogenetic and population evidence for genetic heterogeneity.

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Defending genome integrity during DNA replication: a proposed role for RecQ family helicases

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Human werner syndrome DNA helicase unwinds tetrahelical structures of the fragile X syndrome repeat sequence d(CGG)n

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The Bloom's syndrome helicase unwinds G4 DNA

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Dissociation of the recombination control and the sequence-specific transactivation function of P53

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p53 Protein exhibits 3'-to-5' exonuclease activity

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Human p53 binds Holliday junctions strongly and facilitates their cleavage

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Preferential binding of tumor suppressor p53 to positively or negatively supercoiled DNA involves the C-terminal domain

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Analysis of the binding of p53 to DNAs containing mismatched and bulged bases

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Molecular biology. DNA ends ReQ-uire attention

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Identifiers

DOI

10.1074/JBC.M204111200

1 reference

Consolidated OpenCitations Corpus – April 2017

1 reference

Consolidated OpenCitations Corpus – April 2017

PubMed publication ID

12080066

1 reference

Consolidated OpenCitations Corpus – April 2017