Literature DB >> 9765292

The Bloom's syndrome helicase unwinds G4 DNA.

H Sun1, J K Karow, I D Hickson, N Maizels.   

Abstract

BLM, the gene that is defective in Bloom's syndrome, encodes a protein homologous to RecQ subfamily helicases that functions as a 3'-5' DNA helicase in vitro. We now report that the BLM helicase can unwind G4 DNA. The BLM G4 DNA unwinding activity is ATP-dependent and requires a short 3' region of single-stranded DNA. Strikingly, G4 DNA is a preferred substrate of the BLM helicase, as measured both by efficiency of unwinding and by competition. These results suggest that G4 DNA may be a natural substrate of BLM in vivo and that the failure to unwind G4 DNA may cause the genomic instability and increased frequency of sister chromatid exchange characteristic of Bloom's syndrome.

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Year:  1998        PMID: 9765292     DOI: 10.1074/jbc.273.42.27587

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  228 in total

1.  Palindromes as substrates for multiple pathways of recombination in Escherichia coli.

Authors:  G A Cromie; C B Millar; K H Schmidt; D R Leach
Journal:  Genetics       Date:  2000-02       Impact factor: 4.562

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

Authors:  J K Karow; A Constantinou; J L Li; S C West; I D Hickson
Journal:  Proc Natl Acad Sci U S A       Date:  2000-06-06       Impact factor: 11.205

Review 3.  Immunoglobulin class switch recombination: will genetics provide new clues to mechanism?

Authors:  N Maizels
Journal:  Am J Hum Genet       Date:  1999-05       Impact factor: 11.025

4.  Molecular characterisation of RecQ homologues in Arabidopsis thaliana.

Authors:  F Hartung; H Plchová; H Puchta
Journal:  Nucleic Acids Res       Date:  2000-11-01       Impact factor: 16.971

5.  Potent inhibition of werner and bloom helicases by DNA minor groove binding drugs.

Authors:  R M Brosh; J K Karow; E J White; N D Shaw; I D Hickson; V A Bohr
Journal:  Nucleic Acids Res       Date:  2000-06-15       Impact factor: 16.971

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

Authors:  P Mohaghegh; J K Karow; R M Brosh; V A Bohr; I D Hickson
Journal:  Nucleic Acids Res       Date:  2001-07-01       Impact factor: 16.971

7.  Telomere repeat DNA forms a large non-covalent complex with unique cohesive properties which is dissociated by Werner syndrome DNA helicase in the presence of replication protein A.

Authors:  I Ohsugi; Y Tokutake; N Suzuki; T Ide; M Sugimoto; Y Furuichi
Journal:  Nucleic Acids Res       Date:  2000-09-15       Impact factor: 16.971

8.  Werner syndrome exonuclease catalyzes structure-dependent degradation of DNA.

Authors:  J C Shen; L A Loeb
Journal:  Nucleic Acids Res       Date:  2000-09-01       Impact factor: 16.971

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

Authors:  Leonard Wu; Ian D Hickson
Journal:  Nucleic Acids Res       Date:  2002-11-15       Impact factor: 16.971

10.  Conserved helicase domain of human RecQ4 is required for strand annealing-independent DNA unwinding.

Authors:  Marie L Rossi; Avik K Ghosh; Tomasz Kulikowicz; Deborah L Croteau; Vilhelm A Bohr
Journal:  DNA Repair (Amst)       Date:  2010-05-06
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