| Literature DB >> 9765292 |
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.Entities:
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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