Functional interaction between the Bloom's syndrome helicase and the RAD51 paralog, RAD51L3 (RAD51D) (Q24323327)

1

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Ji-Liang Li

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Leonard Wu

3

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Fiona Caple

4

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Ian D Hickson

Journal of Biological Chemistry

6

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language of work or name

English

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publication date

28 November 2003

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published in

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volume

278

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issue

48

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page(s)

48357-66

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cites work

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A manyfold increase in sister chromatid exchanges in Bloom's syndrome lymphocytes

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The Bloom's syndrome gene product is homologous to RecQ helicases

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Positional cloning of the Werner's syndrome gene

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Mutations in RECQL4 cause a subset of cases of Rothmund-Thomson syndrome

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

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The Saccharomyces cerevisiae Sgs1 helicase efficiently unwinds G-G paired DNAs

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Binding and melting of D-loops by the Bloom syndrome helicase

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

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Biochemical characterization of the DNA helicase activity of the escherichia coli RecQ helicase

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

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Molecular views of recombination proteins and their control

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Functional differences and interactions among the putative RecA homologs Rad51, Rad55, and Rad57.

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Yeast Rad55 and Rad57 proteins form a heterodimer that functions with replication protein A to promote DNA strand exchange by Rad51 recombinase

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Isolation of novel human and mouse genes of the recA/RAD51 recombination-repair gene family

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XRCC2 and XRCC3, new human Rad51-family members, promote chromosome stability and protect against DNA cross-links and other damages

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The mammalian XRCC genes: their roles in DNA repair and genetic stability

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Isolation and cross-sensitivity of X-ray-sensitive mutants of V79-4 hamster cells

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A Chinese hamster ovary cell line hypersensitive to ionizing radiation and deficient in repair replication

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Homologous pairing and ring and filament structure formation activities of the human Xrcc2*Rad51D complex

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Complex formation by the human RAD51C and XRCC3 recombination repair proteins

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Involvement of Rad51C in two distinct protein complexes of Rad51 paralogs in human cells

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Xrcc3 is required for assembly of Rad51 complexes in vivo

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Role of mammalian RAD51L2 (RAD51C) in recombination and genetic stability

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XRCC2 is a nuclear RAD51-like protein required for damage-dependent RAD51 focus formation without the need for ATP binding

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

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Replication protein A physically interacts with the Bloom's syndrome protein and stimulates its helicase activity

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Characterization of the DNA-unwinding activity of human RECQ1, a helicase specifically stimulated by human replication protein A.

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

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The RAD51 family member, RAD51L3, is a DNA-stimulated ATPase that forms a complex with XRCC2

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The Bloom's syndrome gene product interacts with topoisomerase III

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The Bloom's syndrome helicase stimulates the activity of human topoisomerase IIIalpha

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

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Increased error-prone non homologous DNA end-joining--a proposed mechanism of chromosomal instability in Bloom's syndrome

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Defending genome integrity during S-phase: putative roles for RecQ helicases and topoisomerase III.

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Recombinational repair and restart of damaged replication forks.

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Different roles for nonhomologous end joining and homologous recombination following replication arrest in mammalian cells

21 January 2018

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rqh1+, a fission yeast gene related to the Bloom's and Werner's syndrome genes, is required for reversible S phase arrest

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Holliday junction binding activity of the human Rad51B protein

21 January 2018

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

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7 January 2021

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7 January 2021

Mammalian recombination-repair genes XRCC2 and XRCC3 promote correct chromosome segregation

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7 January 2021

The Bloom's syndrome helicase unwinds G4 DNA

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7 January 2021

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

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7 January 2021